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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Systems biology of cisplatin resistance: past, present and future</title><author><name sortKey="Galluzzi, L" sort="Galluzzi, L" uniqKey="Galluzzi L" first="L" last="Galluzzi">L. Galluzzi</name><affiliation><nlm:aff id="aff1"><institution>Gustave Roussy</institution>, Villejuif,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff2"><institution>Université Paris Descartes/Paris V, Sorbonne Paris Cité</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff3"><institution>Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers</institution>, Paris,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Vitale, I" sort="Vitale, I" uniqKey="Vitale I" first="I" last="Vitale">I. Vitale</name><affiliation><nlm:aff id="aff4"><institution>Regina Elena National Cancer Institute</institution>, Rome,<country>Italy</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff5"><institution>National Institute of Health</institution>, Rome,<country>Italy</country></nlm:aff></affiliation></author><author><name sortKey="Michels, J" sort="Michels, J" uniqKey="Michels J" first="J" last="Michels">J. Michels</name><affiliation><nlm:aff id="aff1"><institution>Gustave Roussy</institution>, Villejuif,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff3"><institution>Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff6"><institution>INSERM, U848</institution>, Villejuif,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Brenner, C" sort="Brenner, C" uniqKey="Brenner C" first="C" last="Brenner">C. Brenner</name><affiliation><nlm:aff id="aff7"><institution>INSERM, UMRS 769; LabEx LERMIT</institution>, Châtenay Malabry,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff8"><institution>Faculté de Pharmacie, Université de Paris Sud/Paris XI</institution>, Châtenay Malabry,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Szabadkai, G" sort="Szabadkai, G" uniqKey="Szabadkai G" first="G" last="Szabadkai">G. Szabadkai</name><affiliation><nlm:aff id="aff9"><institution>Department of Cell and Developmental Biology, Consortium for Mitochondrial Research, University College London</institution>, London,<country>UK</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff10"><institution>Department of Biomedical Sciences, Università Degli Studi di Padova</institution>, Padova,<country>Italy</country></nlm:aff></affiliation></author><author><name sortKey="Harel Bellan, A" sort="Harel Bellan, A" uniqKey="Harel Bellan A" first="A" last="Harel-Bellan">A. Harel-Bellan</name><affiliation><nlm:aff id="aff11"><institution>Laboratoire Epigenetique et Cancer, Université de Paris Sud/Paris XI</institution>, Gif-Sur-Yvette,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff12"><institution>CNRS, FRE3377</institution>, Gif-Sur-Yvette,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff13"><institution>Commissariat à l'Energie Atomique (CEA)</institution>, Saclay,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Castedo, M" sort="Castedo, M" uniqKey="Castedo M" first="M" last="Castedo">M. Castedo</name><affiliation><nlm:aff id="aff1"><institution>Gustave Roussy</institution>, Villejuif,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff3"><institution>Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff6"><institution>INSERM, U848</institution>, Villejuif,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Kroemer, G" sort="Kroemer, G" uniqKey="Kroemer G" first="G" last="Kroemer">G. Kroemer</name><affiliation><nlm:aff id="aff2"><institution>Université Paris Descartes/Paris V, Sorbonne Paris Cité</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff3"><institution>Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff6"><institution>INSERM, U848</institution>, Villejuif,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff14"><institution>Pôle de Biologie, Hôpital Européen Georges Pompidou, AP-HP</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff15"><institution>Metabolomics and Cell Biology Platforms, Gustave Roussy</institution>, Villejuif,<country>France</country></nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">24874729</idno><idno type="pmc">4047912</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047912</idno><idno type="RBID">PMC:4047912</idno><idno type="doi">10.1038/cddis.2013.428</idno><date when="2014">2014</date><idno type="wicri:Area/Pmc/Corpus">000029</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000029</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Systems biology of cisplatin resistance: past, present and future</title><author><name sortKey="Galluzzi, L" sort="Galluzzi, L" uniqKey="Galluzzi L" first="L" last="Galluzzi">L. Galluzzi</name><affiliation><nlm:aff id="aff1"><institution>Gustave Roussy</institution>, Villejuif,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff2"><institution>Université Paris Descartes/Paris V, Sorbonne Paris Cité</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff3"><institution>Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers</institution>, Paris,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Vitale, I" sort="Vitale, I" uniqKey="Vitale I" first="I" last="Vitale">I. Vitale</name><affiliation><nlm:aff id="aff4"><institution>Regina Elena National Cancer Institute</institution>, Rome,<country>Italy</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff5"><institution>National Institute of Health</institution>, Rome,<country>Italy</country></nlm:aff></affiliation></author><author><name sortKey="Michels, J" sort="Michels, J" uniqKey="Michels J" first="J" last="Michels">J. Michels</name><affiliation><nlm:aff id="aff1"><institution>Gustave Roussy</institution>, Villejuif,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff3"><institution>Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff6"><institution>INSERM, U848</institution>, Villejuif,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Brenner, C" sort="Brenner, C" uniqKey="Brenner C" first="C" last="Brenner">C. Brenner</name><affiliation><nlm:aff id="aff7"><institution>INSERM, UMRS 769; LabEx LERMIT</institution>, Châtenay Malabry,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff8"><institution>Faculté de Pharmacie, Université de Paris Sud/Paris XI</institution>, Châtenay Malabry,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Szabadkai, G" sort="Szabadkai, G" uniqKey="Szabadkai G" first="G" last="Szabadkai">G. Szabadkai</name><affiliation><nlm:aff id="aff9"><institution>Department of Cell and Developmental Biology, Consortium for Mitochondrial Research, University College London</institution>, London,<country>UK</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff10"><institution>Department of Biomedical Sciences, Università Degli Studi di Padova</institution>, Padova,<country>Italy</country></nlm:aff></affiliation></author><author><name sortKey="Harel Bellan, A" sort="Harel Bellan, A" uniqKey="Harel Bellan A" first="A" last="Harel-Bellan">A. Harel-Bellan</name><affiliation><nlm:aff id="aff11"><institution>Laboratoire Epigenetique et Cancer, Université de Paris Sud/Paris XI</institution>, Gif-Sur-Yvette,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff12"><institution>CNRS, FRE3377</institution>, Gif-Sur-Yvette,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff13"><institution>Commissariat à l'Energie Atomique (CEA)</institution>, Saclay,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Castedo, M" sort="Castedo, M" uniqKey="Castedo M" first="M" last="Castedo">M. Castedo</name><affiliation><nlm:aff id="aff1"><institution>Gustave Roussy</institution>, Villejuif,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff3"><institution>Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff6"><institution>INSERM, U848</institution>, Villejuif,<country>France</country></nlm:aff></affiliation></author><author><name sortKey="Kroemer, G" sort="Kroemer, G" uniqKey="Kroemer G" first="G" last="Kroemer">G. Kroemer</name><affiliation><nlm:aff id="aff2"><institution>Université Paris Descartes/Paris V, Sorbonne Paris Cité</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff3"><institution>Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff6"><institution>INSERM, U848</institution>, Villejuif,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff14"><institution>Pôle de Biologie, Hôpital Européen Georges Pompidou, AP-HP</institution>, Paris,<country>France</country></nlm:aff></affiliation><affiliation><nlm:aff id="aff15"><institution>Metabolomics and Cell Biology Platforms, Gustave Roussy</institution>, Villejuif,<country>France</country></nlm:aff></affiliation></author></analytic><series><title level="j">Cell Death & Disease</title><idno type="eISSN">2041-4889</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>The platinum derivative <italic>cis</italic>-diamminedichloroplatinum(II), best known as cisplatin, is currently employed for the clinical management of patients affected by testicular, ovarian, head and neck, colorectal, bladder and lung cancers. For a long time, the antineoplastic effects of cisplatin have been fully ascribed to its ability to generate unrepairable DNA lesions, hence inducing either a permanent proliferative arrest known as cellular senescence or the mitochondrial pathway of apoptosis. Accumulating evidence now suggests that the cytostatic and cytotoxic activity of cisplatin involves both a nuclear and a cytoplasmic component. Despite the unresolved issues regarding its mechanism of action, the administration of cisplatin is generally associated with high rates of clinical responses. However, in the vast majority of cases, malignant cells exposed to cisplatin activate a multipronged adaptive response that renders them less susceptible to the antiproliferative and cytotoxic effects of the drug, and eventually resume proliferation. Thus, a large fraction of cisplatin-treated patients is destined to experience therapeutic failure and tumor recurrence. Throughout the last four decades great efforts have been devoted to the characterization of the molecular mechanisms whereby neoplastic cells progressively lose their sensitivity to cisplatin. The advent of high-content and high-throughput screening technologies has accelerated the discovery of cell-intrinsic and cell-extrinsic pathways that may be targeted to prevent or reverse cisplatin resistance in cancer patients. Still, the multifactorial and redundant nature of this phenomenon poses a significant barrier against the identification of effective chemosensitization strategies. Here, we discuss recent systems biology studies aimed at deconvoluting the complex circuitries that underpin cisplatin resistance, and how their findings might drive the development of rational approaches to tackle this clinically relevant problem.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Peyrone, M" uniqKey="Peyrone M">M Peyrone</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Burchenal, Jh" uniqKey="Burchenal J">JH Burchenal</name></author><author><name sortKey="Kalaher, K" uniqKey="Kalaher K">K Kalaher</name></author><author><name sortKey="Dew, K" uniqKey="Dew K">K Dew</name></author><author><name sortKey="Lokys, L" uniqKey="Lokys L">L Lokys</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Rosenberg, B" uniqKey="Rosenberg B">B Rosenberg</name></author><author><name sortKey="Vancamp, L" uniqKey="Vancamp L">L Vancamp</name></author><author><name 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Cell Death Dis</journal-id><journal-id journal-id-type="iso-abbrev">Cell Death Dis</journal-id><journal-title-group><journal-title>Cell Death & Disease</journal-title></journal-title-group><issn pub-type="epub">2041-4889</issn><publisher><publisher-name>Nature Publishing Group</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">24874729</article-id><article-id pub-id-type="pmc">4047912</article-id><article-id pub-id-type="pii">cddis2013428</article-id><article-id pub-id-type="doi">10.1038/cddis.2013.428</article-id><article-categories><subj-group subj-group-type="heading"><subject>Review</subject></subj-group></article-categories><title-group><article-title>Systems biology of cisplatin resistance: past, present and future</article-title><alt-title alt-title-type="running">Systematic approaches to tackle CDDP resistance</alt-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Galluzzi</surname><given-names>L</given-names></name><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="aff" rid="aff2">2</xref><xref ref-type="aff" rid="aff3">3</xref><xref ref-type="author-notes" rid="note1"><sup>16</sup></xref><xref ref-type="corresp" rid="caf1">*</xref></contrib><contrib contrib-type="author"><name><surname>Vitale</surname><given-names>I</given-names></name><xref ref-type="aff" rid="aff4">4</xref><xref ref-type="aff" rid="aff5">5</xref></contrib><contrib contrib-type="author"><name><surname>Michels</surname><given-names>J</given-names></name><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="aff" rid="aff3">3</xref><xref ref-type="aff" rid="aff6">6</xref></contrib><contrib contrib-type="author"><name><surname>Brenner</surname><given-names>C</given-names></name><xref ref-type="aff" rid="aff7">7</xref><xref ref-type="aff" rid="aff8">8</xref></contrib><contrib contrib-type="author"><name><surname>Szabadkai</surname><given-names>G</given-names></name><xref ref-type="aff" rid="aff9">9</xref><xref ref-type="aff" rid="aff10">10</xref></contrib><contrib contrib-type="author"><name><surname>Harel-Bellan</surname><given-names>A</given-names></name><xref ref-type="aff" rid="aff11">11</xref><xref ref-type="aff" rid="aff12">12</xref><xref ref-type="aff" rid="aff13">13</xref></contrib><contrib contrib-type="author"><name><surname>Castedo</surname><given-names>M</given-names></name><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="aff" rid="aff3">3</xref><xref ref-type="aff" rid="aff6">6</xref></contrib><contrib contrib-type="author"><name><surname>Kroemer</surname><given-names>G</given-names></name><xref ref-type="aff" rid="aff2">2</xref><xref ref-type="aff" rid="aff3">3</xref><xref ref-type="aff" rid="aff6">6</xref><xref ref-type="aff" rid="aff14">14</xref><xref ref-type="aff" rid="aff15">15</xref><xref ref-type="author-notes" rid="note1"><sup>16</sup></xref><xref ref-type="corresp" rid="caf2">*</xref></contrib><aff id="aff1"><label>1</label><institution>Gustave Roussy</institution>, Villejuif,<country>France</country></aff><aff id="aff2"><label>2</label><institution>Université Paris Descartes/Paris V, Sorbonne Paris Cité</institution>, Paris,<country>France</country></aff><aff id="aff3"><label>3</label><institution>Equipe 11 labellisée par la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers</institution>, Paris,<country>France</country></aff><aff id="aff4"><label>4</label><institution>Regina Elena National Cancer Institute</institution>, Rome,<country>Italy</country></aff><aff id="aff5"><label>5</label><institution>National Institute of Health</institution>, Rome,<country>Italy</country></aff><aff id="aff6"><label>6</label><institution>INSERM, U848</institution>, Villejuif,<country>France</country></aff><aff id="aff7"><label>7</label><institution>INSERM, UMRS 769; LabEx LERMIT</institution>, Châtenay Malabry,<country>France</country></aff><aff id="aff8"><label>8</label><institution>Faculté de Pharmacie, Université de Paris Sud/Paris XI</institution>, Châtenay Malabry,<country>France</country></aff><aff id="aff9"><label>9</label><institution>Department of Cell and Developmental Biology, Consortium for Mitochondrial Research, University College London</institution>, London,<country>UK</country></aff><aff id="aff10"><label>10</label><institution>Department of Biomedical Sciences, Università Degli Studi di Padova</institution>, Padova,<country>Italy</country></aff><aff id="aff11"><label>11</label><institution>Laboratoire Epigenetique et Cancer, Université de Paris Sud/Paris XI</institution>, Gif-Sur-Yvette,<country>France</country></aff><aff id="aff12"><label>12</label><institution>CNRS, FRE3377</institution>, Gif-Sur-Yvette,<country>France</country></aff><aff id="aff13"><label>13</label><institution>Commissariat à l'Energie Atomique (CEA)</institution>, Saclay,<country>France</country></aff><aff id="aff14"><label>14</label><institution>Pôle de Biologie, Hôpital Européen Georges Pompidou, AP-HP</institution>, Paris,<country>France</country></aff><aff id="aff15"><label>15</label><institution>Metabolomics and Cell Biology Platforms, Gustave Roussy</institution>, Villejuif,<country>France</country></aff></contrib-group><author-notes><corresp id="caf1"><label>*</label><institution>Université Paris Descartes/Paris V, INSERM, U848, Gustave Roussy</institution>, PR1, 39, rue Camille Desmoulins, Villejuif F-94805, <country>France</country>. Tel: +33 1 4211 4516; Fax: 33 1 4211 6665; E-mail: <email>deadoc@vodafone.it</email></corresp><corresp id="caf2"><label>*</label><institution>INSERM, U848, Gustave Roussy, PR1, 39, rue Camille Desmoulins</institution>, Villejuif F-94805, <country>France</country>. Tel: +33 1 4211 6046; Fax: +33 1 4211 6047; E-mail: <email>kroemer@orange.fr</email></corresp><fn fn-type="present-address" id="note1"><label>16</label><p>Share senior co-authorship.</p></fn></author-notes><pub-date pub-type="ppub"><month>05</month><year>2014</year></pub-date><pub-date pub-type="epub"><day>29</day><month>05</month><year>2014</year></pub-date><pub-date pub-type="pmc-release"><day>1</day><month>5</month><year>2014</year></pub-date><volume>5</volume><issue>5</issue><fpage>e1257</fpage><lpage></lpage><history><date date-type="received"><day>02</day><month>09</month><year>2013</year></date><date date-type="rev-recd"><day>23</day><month>09</month><year>2013</year></date><date date-type="accepted"><day>26</day><month>09</month><year>2013</year></date></history><permissions><copyright-statement>Copyright © 2014 Macmillan Publishers Limited</copyright-statement><copyright-year>2014</copyright-year><copyright-holder>Macmillan Publishers Limited</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-nd/3.0/"><pmc-comment>author-paid</pmc-comment>
<license-p>This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc-nd/3.0/">http://creativecommons.org/licenses/by-nc-nd/3.0/</ext-link></license-p></license></permissions><abstract><p>The platinum derivative <italic>cis</italic>-diamminedichloroplatinum(II), best known as cisplatin, is currently employed for the clinical management of patients affected by testicular, ovarian, head and neck, colorectal, bladder and lung cancers. For a long time, the antineoplastic effects of cisplatin have been fully ascribed to its ability to generate unrepairable DNA lesions, hence inducing either a permanent proliferative arrest known as cellular senescence or the mitochondrial pathway of apoptosis. Accumulating evidence now suggests that the cytostatic and cytotoxic activity of cisplatin involves both a nuclear and a cytoplasmic component. Despite the unresolved issues regarding its mechanism of action, the administration of cisplatin is generally associated with high rates of clinical responses. However, in the vast majority of cases, malignant cells exposed to cisplatin activate a multipronged adaptive response that renders them less susceptible to the antiproliferative and cytotoxic effects of the drug, and eventually resume proliferation. Thus, a large fraction of cisplatin-treated patients is destined to experience therapeutic failure and tumor recurrence. Throughout the last four decades great efforts have been devoted to the characterization of the molecular mechanisms whereby neoplastic cells progressively lose their sensitivity to cisplatin. The advent of high-content and high-throughput screening technologies has accelerated the discovery of cell-intrinsic and cell-extrinsic pathways that may be targeted to prevent or reverse cisplatin resistance in cancer patients. Still, the multifactorial and redundant nature of this phenomenon poses a significant barrier against the identification of effective chemosensitization strategies. Here, we discuss recent systems biology studies aimed at deconvoluting the complex circuitries that underpin cisplatin resistance, and how their findings might drive the development of rational approaches to tackle this clinically relevant problem.</p></abstract><kwd-group><kwd>BCL-2</kwd><kwd>carboplatin</kwd><kwd>CTR1</kwd><kwd>DNA damage response</kwd><kwd>oxaliplatin</kwd><kwd>p53</kwd></kwd-group></article-meta></front><body><sec><title>Facts</title><p><list list-type="bullet"><list-item><p>A large fraction of human malignancies rapidly becomes (or intrinsically is) insensitive to the cytostatic/cytotoxic effects of cisplatin.</p></list-item><list-item><p>Cisplatin resistance is generally multifactorial, that is, it relies on the activation of multiple, non-redundant molecular or cellular circuitries.</p></list-item><list-item><p>Throughout the past two decades, a number of systems biology studies has been performed to obtain additional insights into cisplatin resistance.</p></list-item><list-item><p>The results of such an intense wave of investigation may promote the development of strategies to circumvent this clinically relevant hurdle.</p></list-item></list></p></sec><sec><title>Open Questions</title><p><list list-type="bullet"><list-item><p>The precise molecular mechanisms whereby cisplatin exerts antineoplastic effects have not yet been elucidated.</p></list-item><list-item><p>In particular, it remains unclear to which extent the cytoplasmic and nuclear events elicited by cisplatin contribute to its cytostatic/cytotoxic activity.</p></list-item><list-item><p>Moreover, the possibility that cisplatin resistance may originate (at least in part) from cell-extrinsic (stromal or immune system-related) mechanisms has not yet been investigated in detail.</p></list-item></list></p><p>First described by the Italian chemist Michele Peyrone as early as in 1845, <italic>cis</italic>-diamminedichloroplatinum(II) (CDDP, best known as cisplatin or cisplatinum), is the founding member of a class of antineoplastic agents born in the second half of the 19th century around the peculiar atomic configuration of platinum.<sup><xref ref-type="bibr" rid="bib1">1</xref>, <xref ref-type="bibr" rid="bib2">2</xref></sup> More than 120 years had indeed to pass from Peyrone's observations for the American chemist Barnett Rosenberg to characterize the robust antiproliferative effects of CDDP, first in <italic>Escherichia coli</italic> cultures, then in solid and hematopoietic tumor xenografts.<sup><xref ref-type="bibr" rid="bib3">3</xref>, <xref ref-type="bibr" rid="bib4">4</xref></sup> Rosenberg's findings initiated an intense wave of preclinical and clinical investigation aimed at elucidating not only the molecular mechanisms that underpin the cytostatic/cytotoxic effects of CDDP, but also its safety and therapeutic profile.<sup><xref ref-type="bibr" rid="bib5">5</xref>, <xref ref-type="bibr" rid="bib6">6</xref>, <xref ref-type="bibr" rid="bib7">7</xref></sup> Such an experimental effort culminated in 1978 with the approval of CDDP by the US Food and Drug Administration (FDA) for use in testicular and bladder cancer patients.<sup><xref ref-type="bibr" rid="bib7">7</xref></sup> Since then, CDDP has been licensed worldwide for the treatment of multiple other solid neoplasms, including head and neck, lung, colorectal and ovarian cancers.<sup><xref ref-type="bibr" rid="bib5">5</xref>, <xref ref-type="bibr" rid="bib8">8</xref>, <xref ref-type="bibr" rid="bib9">9</xref></sup> Thus, during the last 35 years, several millions of cancer patients have received CDDP-based antineoplastic regimens, either as part of consolidated therapeutic procedures or in the context of clinical studies. Unfortunately, CDDP-based chemo(radio)therapy was often destined to fail.</p><p>As a matter of fact, CDDP is highly efficient only against testicular germ cell cancer, leading to a durable complete remission in >80% of the patients.<sup><xref ref-type="bibr" rid="bib10">10</xref>, <xref ref-type="bibr" rid="bib11">11</xref></sup> Conversely, the clinical responses elicited by CDDP-based chemo(radio)therapeutic regimens in patients affected by other solid tumors (e.g., ovarian carcinoma) are temporary and vanish as malignant cells become chemoresistant. Moreover, a significant fraction of lung, prostate and colorectal cancer patients bears neoplastic lesions that are intrinsically resistant to the cytostatic/cytotoxic activity of CDDP.<sup><xref ref-type="bibr" rid="bib12">12</xref>, <xref ref-type="bibr" rid="bib13">13</xref>, <xref ref-type="bibr" rid="bib14">14</xref></sup> Thus, although the use of CDDP (which is generally administered i.v. as a short-term infusion in physiological saline) has been associated with mild-to-moderate nephrotoxic, neurotoxic, cardiotoxic and ototoxic side effects,<sup><xref ref-type="bibr" rid="bib7">7</xref>, <xref ref-type="bibr" rid="bib15">15</xref></sup> chemoresistance (be it intrinsic or acquired) constitutes the most prominent obstacle against the use of this drug. The biological reasons underlying the exquisite sensitivity of testicular germ cell cancers to CDDP have not been completely elucidated. Indeed, although defects in several DNA repair pathways (see below) have been associated with improved disease outcome in CDDP-treated testicular germ cell cancer patients,<sup><xref ref-type="bibr" rid="bib16">16</xref>, <xref ref-type="bibr" rid="bib17">17</xref>, <xref ref-type="bibr" rid="bib18">18</xref>, <xref ref-type="bibr" rid="bib19">19</xref></sup> additional hitherto unidentified factors are likely to influence this phenomenon.</p><p>In the early 1980s, investigators and clinicians began to refocus their attention on the development of CDDP derivatives that would elicit robust therapeutic responses accompanied by clinically manageable side effects. Such an effort led to the discovery of two additional platinum derivatives that are nowadays approved by FDA for use in cancer patients: <italic>cis</italic>-diammine (cyclobutane-1,1-dicarboxylate-<italic>O</italic>,<italic>O</italic>′) platinum(II) (carboplatin) and [(1<italic>R</italic>,2<italic>R</italic>)-cyclohexane-1,2-diamine](ethanedioato-<italic>O</italic>,<italic>O</italic>')platinum(II) (oxaliplatin).<sup><xref ref-type="bibr" rid="bib20">20</xref>, <xref ref-type="bibr" rid="bib21">21</xref></sup> The former has been licensed in 1989 for the treatment of ovarian cancer,<sup><xref ref-type="bibr" rid="bib20">20</xref></sup> whereas the latter has entered clinical practice in 2002, as part of a 5-fluorouracil (5-FU)- and folinic acid-containing cocktail (the so-called FOLFOX regimen) that is routinely employed as a neo-adjuvant or adjuvant intervention in colorectal cancer patients.<sup><xref ref-type="bibr" rid="bib21">21</xref></sup> Carboplatin and CDDP exert antineoplastic effects via very similar, if not undistinguishable, mechanisms, reflecting the fact that the active forms of these drugs are identical. Still, carboplatin appears to be less nephro- and neurotoxic than CDDP, perhaps reflecting its reduced biological potency.<sup><xref ref-type="bibr" rid="bib22">22</xref></sup> Conversely, oxaliplatin and CDDP constitute two chemically distinct entities and as such exhibit distinct pharmacological and immunological properties.<sup><xref ref-type="bibr" rid="bib23">23</xref>, <xref ref-type="bibr" rid="bib24">24</xref>, <xref ref-type="bibr" rid="bib25">25</xref></sup> Nonetheless, a significant proportion of CDDP-insensitive tumors is resistant not only to carboplatin but also to oxaliplatin as well as to a large array of antineoplastic agents with a completely unrelated mechanism of action.<sup><xref ref-type="bibr" rid="bib26">26</xref>, <xref ref-type="bibr" rid="bib27">27</xref>, <xref ref-type="bibr" rid="bib28">28</xref>, <xref ref-type="bibr" rid="bib29">29</xref>, <xref ref-type="bibr" rid="bib30">30</xref>, <xref ref-type="bibr" rid="bib31">31</xref>, <xref ref-type="bibr" rid="bib32">32</xref>, <xref ref-type="bibr" rid="bib33">33</xref>, <xref ref-type="bibr" rid="bib34">34</xref>, <xref ref-type="bibr" rid="bib35">35</xref>, <xref ref-type="bibr" rid="bib36">36</xref></sup> These observations, which reflect the multilevel and multifactorial nature of CDDP resistance (see below), have fostered the development of additional platinum derivatives, including amminedichloro(2-methylpyridine)platinum (picoplatin) and (<italic>OC</italic>-6-43)-bis(acetato)amminedichloro(cyclohexylamine)platinum (satraplatin). As it stands, however, neither picoplatin- nor satraplatin-containing regimens provide consistent advantages over CDDP-, oxaliplatin- and carboplatin-based chemotherapy.<sup><xref ref-type="bibr" rid="bib37">37</xref>, <xref ref-type="bibr" rid="bib38">38</xref>, <xref ref-type="bibr" rid="bib39">39</xref>, <xref ref-type="bibr" rid="bib40">40</xref></sup> Thus, the interest in developing novel platinum derivatives as well as clinically applicable strategies to increase the sensitivity of human neoplasms to CDDP remains high.</p><p>In this review, we summarize the mechanisms whereby CDDP exerts antineoplastic effects as well as the major determinants of CDDP resistance, laying special emphasis on recent systems biology studies aimed at avoiding or overcoming this crucial clinical issue.</p></sec><sec><title>Mode of Action</title><p>CDDP is chemically inert until one or both of its <italic>cis</italic> chloro groups are replaced by water molecules.<sup><xref ref-type="bibr" rid="bib41">41</xref>, <xref ref-type="bibr" rid="bib42">42</xref></sup> Such an ‘aquation' occurs spontaneously in the cytoplasm, presumably due to the relatively low concentration of chloride ions (∼2–10 mM, as compared with ∼100 mM in the extracellular space).<sup><xref ref-type="bibr" rid="bib43">43</xref>, <xref ref-type="bibr" rid="bib44">44</xref></sup> Mono- and bi-aquated forms of CDDP are highly electrophilic and hence prone to form covalent bonds with methionine as well as with a large panel of cysteine-containing peptides and polypeptides, including reduced glutathione (GSH) and metallothioneins.<sup><xref ref-type="bibr" rid="bib45">45</xref></sup> The interaction between aquated CDDP and endogenous nucleophiles has dual consequences. On one hand, it depletes the cytosol of reducing equivalents, hence promoting the establishment of oxidative stress, which may have direct cytotoxic effects or provoke DNA damage (see below).<sup><xref ref-type="bibr" rid="bib46">46</xref>, <xref ref-type="bibr" rid="bib47">47</xref></sup> On the other hand, it results in the inactivation of (at least a fraction of) chemically reactive CDDP, hence functioning as a cytoprotective buffer.<sup><xref ref-type="bibr" rid="bib12">12</xref>, <xref ref-type="bibr" rid="bib48">48</xref></sup></p><p>Upon aquation, CDDP also binds with high affinity to mitochondrial and nuclear DNA, in particular to nucleophilic N7 sites on purines, thus favoring the generation of heterotypic protein–DNA complexes as well as homotypic inter- and intra-strand DNA adducts.<sup><xref ref-type="bibr" rid="bib49">49</xref>, <xref ref-type="bibr" rid="bib50">50</xref>, <xref ref-type="bibr" rid="bib51">51</xref></sup> If limited in amount, the DNA lesions provoked by CDDP can be recognized and safely removed by several repair systems that normally operate in the context of a temporary cell cycle arrest.<sup><xref ref-type="bibr" rid="bib52">52</xref>, <xref ref-type="bibr" rid="bib53">53</xref>, <xref ref-type="bibr" rid="bib54">54</xref>, <xref ref-type="bibr" rid="bib55">55</xref>, <xref ref-type="bibr" rid="bib56">56</xref></sup> Conversely, when the CDDP-induced DNA damage is irreparable, either such a cell cycle arrest becomes permanent (an oncosuppressive response known as cellular senescence)<sup><xref ref-type="bibr" rid="bib57">57</xref>, <xref ref-type="bibr" rid="bib58">58</xref></sup> or cells become committed to die, most often via mitochondrial apoptosis.<sup><xref ref-type="bibr" rid="bib59">59</xref>, <xref ref-type="bibr" rid="bib60">60</xref>, <xref ref-type="bibr" rid="bib61">61</xref>, <xref ref-type="bibr" rid="bib62">62</xref>, <xref ref-type="bibr" rid="bib63">63</xref>, <xref ref-type="bibr" rid="bib64">64</xref></sup> Both these processes can be initiated by the sequential activation of ATM- and RAD3-related protein (ATR, a sensor of DNA damage) and checkpoint kinase 1 (CHEK1, its major downstream effector), eventually resulting in the stabilizing phosphorylation of the oncosuppressor protein p53.<sup><xref ref-type="bibr" rid="bib65">65</xref>, <xref ref-type="bibr" rid="bib66">66</xref>, <xref ref-type="bibr" rid="bib67">67</xref>, <xref ref-type="bibr" rid="bib68">68</xref>, <xref ref-type="bibr" rid="bib69">69</xref></sup> A precise description of the molecular mechanisms whereby an excess of DNA lesions promotes widespread mitochondrial outer membrane permeabilization (MOMP), and hence cell death, exceeds the scope of this review and can be found in other publications.<sup><xref ref-type="bibr" rid="bib65">65</xref>, <xref ref-type="bibr" rid="bib66">66</xref>, <xref ref-type="bibr" rid="bib67">67</xref>, <xref ref-type="bibr" rid="bib70">70</xref>, <xref ref-type="bibr" rid="bib71">71</xref></sup></p><p>Importantly, it is now clear that the cytostatic/cytotoxic effects of CDDP do not represent a mere consequence of its genotoxic activity, but originate from both nuclear and cytoplasmic signaling pathways.<sup><xref ref-type="bibr" rid="bib48">48</xref>, <xref ref-type="bibr" rid="bib72">72</xref></sup> In line with this notion, (i) only ∼1% of intracellular CDDP forms covalent bonds with nuclear DNA<sup><xref ref-type="bibr" rid="bib73">73</xref></sup> and (ii) CDDP (as well as oxaliplatin) exerts prominent cytotoxic effects in enucleated cells (cytoplasts).<sup><xref ref-type="bibr" rid="bib51">51</xref>, <xref ref-type="bibr" rid="bib74">74</xref>, <xref ref-type="bibr" rid="bib75">75</xref>, <xref ref-type="bibr" rid="bib76">76</xref>, <xref ref-type="bibr" rid="bib77">77</xref>, <xref ref-type="bibr" rid="bib78">78</xref></sup> The molecular mechanisms that underlie the cytotoxic potential of cytoplasmic CDDP are poorly understood, yet may involve: (i) the accumulation of reactive oxygen species (ROS) and nitric oxide (NO), which not only exacerbate CDDP genotoxicity but also exert direct cytotoxic effects by favoring the opening of the so-called permeability transition pore complex (PTPC);<sup><xref ref-type="bibr" rid="bib70">70</xref>, <xref ref-type="bibr" rid="bib79">79</xref>, <xref ref-type="bibr" rid="bib80">80</xref></sup> (ii) the transduction of a MOMP-stimulatory signal via the pro-apoptotic BCL-2 family member BAK1, the PTPC component voltage-dependent anion channel 1 (VDAC1) and the BAK1 homolog BAX;<sup><xref ref-type="bibr" rid="bib81">81</xref>, <xref ref-type="bibr" rid="bib82">82</xref></sup> (iii) the activation of a cytoplasmic pool of p53 that is capable of promoting MOMP via various mechanisms<sup><xref ref-type="bibr" rid="bib83">83</xref>, <xref ref-type="bibr" rid="bib84">84</xref>, <xref ref-type="bibr" rid="bib85">85</xref>, <xref ref-type="bibr" rid="bib86">86</xref></sup> and (iv) in specific cellular models (see below), the establishment of an endoplasmic reticulum (ER) stress response.<sup><xref ref-type="bibr" rid="bib77">77</xref>, <xref ref-type="bibr" rid="bib87">87</xref></sup></p><p>The relative contribution of all these nuclear and cytoplasmic effects to the cytostatic/cytotoxic activity of CDDP remains to be deciphered and may exhibit a consistent degree of context dependency (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p></sec><sec><title>Mechanisms of Resistance</title><p>We have recently discussed the molecular mechanisms that reduce the sensitivity of malignant cells to CDDP, and classified them based on functional and hierarchical parameters. In particular, we proposed that CDDP resistance can surge from alterations (i) in processes that precede the binding of CDDP to its actual targets, including DNA and cytoplasmic structures (pre-target resistance), (ii) directly related to the molecular damage provoked by CDDP (on-target resistance), (iii) in the lethal signaling pathways triggered by such molecular lesions (post-target resistance) and (iv) influencing molecular circuitries that are not (or at least have not yet been) intimately associated with CDDP-elicited signals (off-target resistance).<sup><xref ref-type="bibr" rid="bib48">48</xref></sup></p><sec><title>Pre-target resistance</title><p>CDDP resistance can develop along with alterations that reduce the amount of aquated CDDP forms in the cytoplasm. Although for a long time CDDP has been believed to get access to the cytoplasmic compartment by passively diffusing across the plasma membrane,<sup><xref ref-type="bibr" rid="bib42">42</xref>, <xref ref-type="bibr" rid="bib88">88</xref></sup> it is now clear that the majority of CDDP is actively moved in and out of the cell by copper transporters. In particular, copper transporter 1 (CTR1) has turned out to mediate a significant fraction of CDDP intake,<sup><xref ref-type="bibr" rid="bib89">89</xref>, <xref ref-type="bibr" rid="bib90">90</xref>, <xref ref-type="bibr" rid="bib91">91</xref>, <xref ref-type="bibr" rid="bib92">92</xref>, <xref ref-type="bibr" rid="bib93">93</xref></sup> whereas ATPase, Cu<sup>2+</sup> transporting, <italic>β</italic> polypeptide (ATP7B), a Cu<sup>2+</sup>-extruding P-type ATPase involved in the pathogenesis of Wilson's disease,<sup><xref ref-type="bibr" rid="bib94">94</xref></sup> plays a significant role in CDDP export.<sup><xref ref-type="bibr" rid="bib90">90</xref>, <xref ref-type="bibr" rid="bib95">95</xref></sup> In line with this notion, alterations in the expression level, subcellular localization and/or functionality of CTR1 and ATP7B have been associated with CDDP resistance, both in preclinical models and in cancer patients.<sup><xref ref-type="bibr" rid="bib90">90</xref>, <xref ref-type="bibr" rid="bib91">91</xref>, <xref ref-type="bibr" rid="bib93">93</xref>, <xref ref-type="bibr" rid="bib96">96</xref>, <xref ref-type="bibr" rid="bib97">97</xref>, <xref ref-type="bibr" rid="bib98">98</xref>, <xref ref-type="bibr" rid="bib99">99</xref>, <xref ref-type="bibr" rid="bib100">100</xref>, <xref ref-type="bibr" rid="bib101">101</xref>, <xref ref-type="bibr" rid="bib102">102</xref></sup> Promising (though very preliminary) results from a pilot clinical trial investigating the safety and chemosensitizing potential of trientine (a copper chelator) plus platinum-based chemotherapy in advanced cancer patients (NCT01178112) have recently been disseminated.<sup><xref ref-type="bibr" rid="bib102">102</xref>, <xref ref-type="bibr" rid="bib103">103</xref>, <xref ref-type="bibr" rid="bib104">104</xref></sup></p><p>Other plasma membrane transporters have been suggested to contribute to the extrusion of CDDP (hence promoting CDDP resistance in preclinical as well as clinical settings), notably ATP-binding cassette, subfamily C (CFTR/MRP), member 2 (ABCC2), best known as multidrug resistance-associated protein 2 (MRP2)<sup><xref ref-type="bibr" rid="bib105">105</xref>, <xref ref-type="bibr" rid="bib106">106</xref>, <xref ref-type="bibr" rid="bib107">107</xref>, <xref ref-type="bibr" rid="bib108">108</xref>, <xref ref-type="bibr" rid="bib109">109</xref></sup> and ATPase, class VI, type 11B (ATP11B).<sup><xref ref-type="bibr" rid="bib110">110</xref></sup> Moreover, CDDP-resistant cancer cells may exhibit increased levels of GSH, the enzyme that catalyzes GSH synthesis (i.e., <italic>γ</italic>-glutamylcysteine synthetase), the enzyme that conjugates CDDP with GSH (i.e., glutathione S-transferase), or metallothioneins.<sup><xref ref-type="bibr" rid="bib111">111</xref>, <xref ref-type="bibr" rid="bib112">112</xref>, <xref ref-type="bibr" rid="bib113">113</xref>, <xref ref-type="bibr" rid="bib114">114</xref></sup> Although none of these alterations has been shown to be clinically relevant, all of them may contribute to pre-target resistance by incrementing the capacity of the cytoplasmic CDDP buffer.</p></sec><sec><title>On-target resistance</title><p>The sensitivity of cancer cells to the cytostatic/cytotoxic effects of CDDP is limited in the presence of a proficient DNA repair apparatus. In particular, the nucleotide excision repair (NER) system is believed to resolve the majority of DNA lesions provoked by CDDP,<sup><xref ref-type="bibr" rid="bib53">53</xref>, <xref ref-type="bibr" rid="bib54">54</xref></sup> although components of the mismatch repair (MMR) machinery have also been implicated in this process (at least in its detection, as opposed to resolution, phase).<sup><xref ref-type="bibr" rid="bib55">55</xref></sup> In line with this notion, an increased NER proficiency has been associated with CDDP resistance <italic>in vitro</italic>, in murine models as well as in cohorts of cancer patients.<sup><xref ref-type="bibr" rid="bib115">115</xref>, <xref ref-type="bibr" rid="bib116">116</xref>, <xref ref-type="bibr" rid="bib117">117</xref>, <xref ref-type="bibr" rid="bib118">118</xref>, <xref ref-type="bibr" rid="bib119">119</xref>, <xref ref-type="bibr" rid="bib120">120</xref>, <xref ref-type="bibr" rid="bib121">121</xref>, <xref ref-type="bibr" rid="bib122">122</xref>, <xref ref-type="bibr" rid="bib123">123</xref></sup> Convenient biomarkers for assessing NER proficiency in human tumors are still missing, as the actual predictive value of excision repair cross-complementing rodent repair deficiency, complementation group 1 (ERCC1) expression levels (first proposed in 2006),<sup><xref ref-type="bibr" rid="bib118">118</xref></sup> has recently been reconsidered.<sup><xref ref-type="bibr" rid="bib124">124</xref></sup> The MMR system is believed to detect DNA adducts caused by CDDP, engage in their repair and ultimately fail, thus transmitting a pro-apoptotic signal.<sup><xref ref-type="bibr" rid="bib125">125</xref></sup> Accordingly, genes encoding MMR components such as <italic>mutS</italic> homolog 2 (MSH2) and <italic>mutL</italic> homolog 1 (MLH1) are frequently mutated or downregulated in the context-acquired CDDP resistance.<sup><xref ref-type="bibr" rid="bib126">126</xref>, <xref ref-type="bibr" rid="bib127">127</xref>, <xref ref-type="bibr" rid="bib128">128</xref>, <xref ref-type="bibr" rid="bib129">129</xref></sup> Moreover, non-small cell lung carcinoma (NSCLC) lesions expressing high MSH2 levels exhibit an improved prognosis upon surgical resection (in the absence of adjuvant chemotherapy).<sup><xref ref-type="bibr" rid="bib130">130</xref></sup> Thus, high expression levels of MMR components may exert a positive influence both on the propensity of chemotherapy-naive tumors to relapse (perhaps because MMR limits the accumulation of additional genetic alterations) and on the probability that neoplasms exposed to CDDP become chemoresistant. <italic>MLH1</italic> mutations are also associated with increased rates of translesion synthesis (TLS), the process whereby DNA is replicated (by a peculiar class of polymerases) in spite of unrepaired lesions.<sup><xref ref-type="bibr" rid="bib131">131</xref></sup> In line with this notion, defects in TLS polymerases including polymerase (DNA-directed), <italic>η</italic> (POLH) and REV3-like, polymerase (DNA directed), <italic>ζ</italic>, catalytic subunit (REV3L) have been linked to increased CDDP sensitivity <italic>in vitro</italic>.<sup><xref ref-type="bibr" rid="bib132">132</xref>, <xref ref-type="bibr" rid="bib133">133</xref>, <xref ref-type="bibr" rid="bib134">134</xref>, <xref ref-type="bibr" rid="bib135">135</xref></sup> However, compelling clinical evidence in support of the translational relevance of these findings is elusive.</p><p>CDDP-elicited DNA adducts can engender double-strand breaks (DSBs), which are normally repaired along with DNA synthesis (or shortly after) via homologous recombination (HR).<sup><xref ref-type="bibr" rid="bib136">136</xref></sup> Accordingly, HR-deficient neoplasms, such as those bearing loss-of-function mutations in the genes encoding breast cancer 1, early onset (BRCA1) or breast cancer 2, early onset (BRCA2),<sup><xref ref-type="bibr" rid="bib137">137</xref>, <xref ref-type="bibr" rid="bib138">138</xref></sup> are generally more susceptible to the genotoxic effects of CDDP than HR-proficient cancers of the same type.<sup><xref ref-type="bibr" rid="bib139">139</xref>, <xref ref-type="bibr" rid="bib140">140</xref>, <xref ref-type="bibr" rid="bib141">141</xref></sup> Moreover, the appearance of compensatory mutations in <italic>BRCA1</italic> and <italic>BRCA2</italic> that restore the functionality of HR has been show to favor CDDP resistance in breast carcinoma cells.<sup><xref ref-type="bibr" rid="bib142">142</xref></sup> Mutations of this type not only have been associated with the resistance of ovarian carcinoma to platinum-based chemotherapy<sup><xref ref-type="bibr" rid="bib142">142</xref>, <xref ref-type="bibr" rid="bib143">143</xref></sup> but also appear to influence the sensitivity of pancreatic and ovarian neoplasms to inhibitors of poly(ADP-ribose) polymerase 1 (PARP1), another important regulator of DNA repair.<sup><xref ref-type="bibr" rid="bib144">144</xref></sup> Of note, while the innate resistance of pancreatic carcinoma cells to CDDP and PARP1 inhibitors resolves simultaneously in response to HR-restoring <italic>BRCA2</italic> mutations,<sup><xref ref-type="bibr" rid="bib143">143</xref></sup> we have recently reported that NSCLC cells cultured for prolonged periods in the presence of subtoxic amounts of CDDP often (but not always) manifest a constitutive hyperactivation of PARP1, hence becoming susceptible to pharmacological or genetic PARP inhibition.<sup><xref ref-type="bibr" rid="bib145">145</xref></sup> In line with these notions, the concomitant administration of CDDP and PARP inhibitors appears to elicit at least additive antineoplastic effects, <italic>in vitro</italic> and <italic>in vivo</italic>.<sup><xref ref-type="bibr" rid="bib146">146</xref>, <xref ref-type="bibr" rid="bib147">147</xref>, <xref ref-type="bibr" rid="bib148">148</xref></sup></p><p>Although the identity of the cytoplasmic components that account for the extranuclear toxicity of CDDP has only recently begun to emerge, these molecules as well as the enzymatic systems that regulate their preservation/turnover may also be involved in the development of on-target CDDP resistance.<sup><xref ref-type="bibr" rid="bib72">72</xref></sup> So far, only a few extranuclear CDDP-binding partners have been identified, including near-to-ubiquitous (e.g., valosin-containing protein), as well as mostly cytosolic (e.g., myosin IIa, HSP90), ribosomal (e.g., ribosomal protein L5), reticular (e.g., calreticulin) and mitochondrial components (e.g., mitochondrial DNA, VDAC1).<sup><xref ref-type="bibr" rid="bib51">51</xref>, <xref ref-type="bibr" rid="bib149">149</xref></sup> Remarkably, human NSCLC cells developing CDDP resistance as they are exposed for long periods to sublethal doses of the drug appear to be positively selected for specific mitochondrial DNA mutations, resulting in partial defects of the respiratory chain.<sup><xref ref-type="bibr" rid="bib150">150</xref>, <xref ref-type="bibr" rid="bib151">151</xref></sup> Two mechanisms that may account for this effect are the compensatory stimulation of mitochondrial biogenesis by retrograde mitochondrio-nuclear signaling and the activation of a peroxisome proliferator-activated receptor <italic>γ</italic>, coactivator 1<italic>β</italic> (PPARGC1B)-dependent (but mitochondrion-independent) signal transduction cascade.<sup><xref ref-type="bibr" rid="bib150">150</xref>, <xref ref-type="bibr" rid="bib152">152</xref></sup> Moreover, both rho<sup>0</sup> cells and cells depleted of VDAC1 by RNA interference are less susceptible to CDDP cytotoxicity than their wild-type counterparts.<sup><xref ref-type="bibr" rid="bib51">51</xref>, <xref ref-type="bibr" rid="bib81">81</xref></sup> In line with this notion, the transfection-enforced overexpression of VDAC1 reportedly sensitizes carcinoma cells to cell death induction by CDDP.<sup><xref ref-type="bibr" rid="bib82">82</xref></sup> However, elevated expression levels of VDAC1 may exert broad chemosensitization effects.<sup><xref ref-type="bibr" rid="bib153">153</xref></sup> Thus, whether these observations constitute examples of <italic>bona fide</italic> on-target resistance or rather reflect the critical role of mitochondria (and in particular of the PTPC) in CDDP-elicited cell death, hence constituting examples of post-target resistance, remains an open conundrum. Along similar lines, although physical interactions between CDDP and cyclin-dependent kinase 2 (CDK2) have not yet been documented, CDK2 has been shown to contribute to extranuclear CDDP toxicity (by inducing ER stress, at least in some cellular models), and CDK2-deficient cells exhibit some extent of CDDP resistance.<sup><xref ref-type="bibr" rid="bib77">77</xref>, <xref ref-type="bibr" rid="bib87">87</xref></sup></p></sec><sec><title>Post-target resistance</title><p>In line with the notion that regulated cell death (be it apoptotic or necrotic) is under the control of a plethora of checkpoints and safeguard mechanisms, post-target CDDP resistance may develop along with a wide panel of alterations in the systems that detect the molecular damage caused by CDDP and convert it into a lethal signal, as well as in the machinery that <italic>de facto</italic> executes cell death.<sup><xref ref-type="bibr" rid="bib12">12</xref>, <xref ref-type="bibr" rid="bib48">48</xref>, <xref ref-type="bibr" rid="bib154">154</xref></sup> Malignant cells are (i) intrinsically more resistant to adverse microenvironmental and intracellular cues than their non-transformed counterparts<sup><xref ref-type="bibr" rid="bib155">155</xref>, <xref ref-type="bibr" rid="bib156">156</xref></sup> and (ii) highly prone to acquire additional genetic and epigenetic alterations.<sup><xref ref-type="bibr" rid="bib157">157</xref>, <xref ref-type="bibr" rid="bib158">158</xref></sup> Thus, (at least some degree of) post-target resistance can be documented in most, if not all, CDDP-exposed tumors. Importantly, post-target CDDP resistance is rarely (if ever) specific, rather extending to other DNA-damaging agents (including radiation),<sup><xref ref-type="bibr" rid="bib27">27</xref>, <xref ref-type="bibr" rid="bib33">33</xref>, <xref ref-type="bibr" rid="bib159">159</xref></sup> as well as to cytotoxic stimuli that engage a wide panel of primary targets (e.g., death receptor agonists).<sup><xref ref-type="bibr" rid="bib160">160</xref></sup></p><p>As a general rule, intracellular stress conditions (such as those elicited by CDDP) promote the rapid activation of an integrated adaptive response aimed at the re-establishment of cellular homeostasis.<sup><xref ref-type="bibr" rid="bib161">161</xref></sup> This is generally accompanied by the emission of robust anti-apoptotic cues and only when homeostasis cannot be restored (for instance, when stress conditions are excessive in intensity or duration) lethal signals are transmitted, <italic>de facto</italic> representing a mechanism for the preservation of organismal homeostasis.<sup><xref ref-type="bibr" rid="bib162">162</xref></sup> In the case of CDDP, these signals consist in (i) the switch of the DNA damage response from a cytoprotective to a cytotoxic mode, followed by the (often, but not always, p53-dependent) activation of BAX and BAK1<sup><xref ref-type="bibr" rid="bib163">163</xref></sup> and (ii) the accumulation of ROS and consequent PTPC opening.<sup><xref ref-type="bibr" rid="bib81">81</xref>, <xref ref-type="bibr" rid="bib164">164</xref></sup> Both these processes eventually promote MOMP, in turn resulting in the functional and physical breakdown of mitochondria followed by the activation of caspase-dependent and independent mechanisms of cell death.<sup><xref ref-type="bibr" rid="bib70">70</xref>, <xref ref-type="bibr" rid="bib165">165</xref></sup> Thus, post-target CDDP resistance has been associated not only with genetic and epigenetic alterations that impair p53 signaling (<italic>in vitro</italic>, in murine tumor models as well as in several distinct clinical scenarios)<sup><xref ref-type="bibr" rid="bib11">11</xref>, <xref ref-type="bibr" rid="bib166">166</xref>, <xref ref-type="bibr" rid="bib167">167</xref>, <xref ref-type="bibr" rid="bib168">168</xref>, <xref ref-type="bibr" rid="bib169">169</xref>, <xref ref-type="bibr" rid="bib170">170</xref></sup> but also with defects in several other pro-apoptotic signal transducers, including mitogen-activated protein kinase 14 (MAPK14, best known as p38<sup>MAPK</sup>) and c-Jun N-terminal kinase 1 (JNK1).<sup><xref ref-type="bibr" rid="bib171">171</xref>, <xref ref-type="bibr" rid="bib172">172</xref></sup> Along similar lines, post-target CDDP resistance appears to be significantly influenced by the expression levels and functional status of BCL-2 family members and caspases, a class of cysteine proteases that has a major role in the execution of apoptotic cell death.<sup><xref ref-type="bibr" rid="bib81">81</xref>, <xref ref-type="bibr" rid="bib173">173</xref>, <xref ref-type="bibr" rid="bib174">174</xref></sup> This said, only a few of these factors have been formally correlated with CDDP resistance in clinical studies, including various BCL-2-like proteins such as BCL-2 itself, BCL-X<sub>L</sub> and MCL-1,<sup><xref ref-type="bibr" rid="bib175">175</xref>, <xref ref-type="bibr" rid="bib176">176</xref>, <xref ref-type="bibr" rid="bib177">177</xref>, <xref ref-type="bibr" rid="bib178">178</xref></sup> survivin, a caspase inhibitor that is often upregulated in response to CDDP,<sup><xref ref-type="bibr" rid="bib179">179</xref>, <xref ref-type="bibr" rid="bib180">180</xref>, <xref ref-type="bibr" rid="bib181">181</xref>, <xref ref-type="bibr" rid="bib182">182</xref></sup> as well as other members of the baculoviral IAP repeat-containing (BIRC) protein family.<sup><xref ref-type="bibr" rid="bib183">183</xref></sup> In line with this notion, small molecules that antagonize the anti-apoptotic effects of BCL-2-like proteins (e.g., ABT-263) as well as IAP inhibitors (e.g., YM155, LY2181308, LBW242) have been intensively investigated in clinical trials, either as standalone anticancer interventions or in combination with various chemotherapeutics including CDDP.<sup><xref ref-type="bibr" rid="bib184">184</xref>, <xref ref-type="bibr" rid="bib185">185</xref>, <xref ref-type="bibr" rid="bib186">186</xref>, <xref ref-type="bibr" rid="bib187">187</xref>, <xref ref-type="bibr" rid="bib188">188</xref></sup> In spite of an acceptable safety profile and promising antineoplastic activity, the clinical development of all these agents appears to stand at an impasse, at least as judged by the low rate of ongoing <italic>versus</italic> completed, terminated or withdrawn trials (source <ext-link ext-link-type="uri" xlink:href="http://www.clinicaltrials.gov">www.clinicaltrials.gov</ext-link>).</p></sec><sec><title>Off-target resistance</title><p>The susceptibility of cancer cells to CDDP can also be limited by off-target mechanisms, that is, molecular circuitries that deliver compensatory survival signals even though they are not directly activated by CDDP.<sup><xref ref-type="bibr" rid="bib48">48</xref></sup> For instance, the overexpression of <italic>v-erb-b2</italic> avian erythroblastic leukemia viral oncogene homolog 2 (ERBB2), which is common in breast and ovarian carcinomas,<sup><xref ref-type="bibr" rid="bib189">189</xref>, <xref ref-type="bibr" rid="bib190">190</xref></sup> has been suggested to promote CDDP resistance not only by delivering robust pro-survival signals via the <italic>v-akt</italic> murine thymoma viral oncogene homolog 1 (AKT1) signaling axis, but also by finely regulating the transitory cell cycle arrest that is required for the repair of CDDP-induced DNA lesions.<sup><xref ref-type="bibr" rid="bib191">191</xref>, <xref ref-type="bibr" rid="bib192">192</xref></sup> Along similar lines, dual-specificity Y-phosphorylation-regulated kinase 1B (DYRK1B, also known as MIRK) appears to sustain CDDP resistance as it favors the expression of various antioxidant enzymes.<sup><xref ref-type="bibr" rid="bib193">193</xref></sup> By augmenting the intracellular pool of antioxidants, DYRK1B may actually reduce the susceptibility of cancer cells to CDDP via on-target, post-target as well as off-target mechanisms.<sup><xref ref-type="bibr" rid="bib48">48</xref></sup> Recently, a poorly characterized transmembrane protein (TMEM205) has been shown to favor CDDP resistance via a molecular cascade that involves the small RAS-like GTPase RAB8A.<sup><xref ref-type="bibr" rid="bib194">194</xref>, <xref ref-type="bibr" rid="bib195">195</xref></sup> Whether this constitutes an off-target mechanism of resistance or rather reflects the inhibition of caspase-9 by AKT1-transduced signals<sup><xref ref-type="bibr" rid="bib196">196</xref></sup> (hence representing a post-target effect) remains to be clarified. Finally, several relatively unspecific adaptive responses to stress have been implicated in CDDP resistance. Such general responses include macroautophagy and the so-called heat-shock response, that is, the adaptation of cells to increased temperatures and other conditions that promote protein unfolding.<sup><xref ref-type="bibr" rid="bib161">161</xref></sup> Thus, various components of the autophagic machinery and several chaperones of the heat-shock protein (HSP) family reportedly impair the cytostatic/cytotoxic response of cultured cancer cells to CDDP.<sup><xref ref-type="bibr" rid="bib149">149</xref>, <xref ref-type="bibr" rid="bib197">197</xref>, <xref ref-type="bibr" rid="bib198">198</xref>, <xref ref-type="bibr" rid="bib199">199</xref>, <xref ref-type="bibr" rid="bib200">200</xref>, <xref ref-type="bibr" rid="bib201">201</xref></sup> Moreover, the expression levels of HSP27 may constitute a predictive biomarkers of clinical responses to CDDP in esophageal squamous cell carcinoma patients.<sup><xref ref-type="bibr" rid="bib202">202</xref></sup></p><p>In conclusion, malignant cells can lose their sensitivity to CDDP owing to a wide panel of molecular and functional alterations, many of which are <italic>a priori</italic> connected to oncogenesis and tumor progression. CDDP resistance is often multifactorial, as it relies on the simultaneous activation of multiple, non-redundant molecular circuitries (<xref ref-type="fig" rid="fig2">Figure 2</xref>).<sup><xref ref-type="bibr" rid="bib48">48</xref>, <xref ref-type="bibr" rid="bib203">203</xref></sup> This obviously poses a major hurdle against the development of therapeutically useful chemosensitization strategies. As summarized below, several systems biology studies have recently been undertaken to address this clinically relevant issue.</p></sec></sec><sec><title>Systems Biology and Cisplatin Resistance</title><p>Throughout the last decade, a huge number of high-content and/or high-throughput studies have been initiated to tackle – by means of an empirical approach – the complex and clinically relevant problem of CDDP resistance. For illustrative purposes, these studies can be classified into three large groups: (i) genomic, transcriptomic, methylomic and proteomic approaches, investigating the correlation between CDDP resistance and gene expression/regulation or the activation of specific signal transduction pathways (in preclinical models or patient material); (ii) large-scale silencing approaches and functional screenings, determining whether the genetic or pharmacological inhibition of specific proteins alters CDDP sensitivity (in preclinical models only) and (iii) multiplex genotyping studies, assessing in a high-throughput manner whether particular (combinations of) single-nucleotide polymorphisms (SNPs) are associated with increased or reduced CDDP sensitivity (in clinical settings). Each of these approaches obviously brings about specific advantages and disadvantages, which we will not systematically discuss here (for further details please consult a recent study by He <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib204">204</xref></sup>). Still, it is important to note that, with a few exceptions (including some genotyping studies), the majority of these strategies have relied on relatively reductionistic models (e.g., cultured cancer cells) or readouts (e.g., mRNA levels in whole-tumor lysates). Considering tumors as relatively homogeneous entities exclusively composed of malignant cells and attributing CDDP resistance only to cancer cell-intrinsic mechanisms (hence neglecting the prominent structural and functional impact of stromal and immune cells) appears indeed as an excessive oversimplification (see below), and may in part explain why clinically applicable strategies for restoring CDDP sensitivity are still missing. Nonetheless, these studies have provided us with ever more precise insights into the molecular mechanisms that account for CDDP resistance, at least at the cell-intrinsic level. Here, we provide an overview of recent systems biology studies (for the most part published in the last 3 years) that have significantly added to our understanding of CDDP resistance (<xref ref-type="supplementary-material" rid="sup1">Supplementary Table 1</xref>).</p><sec><title>Genomic, methylomic, transcriptomic and proteomic approaches</title><p>For nearly one decade, it has been possible – and cost-efficient – to employ microarrays for quantifying (i) variations in gene copy number, by comparative genomic hybridization (CGH), (ii) the abundance of mRNAs and (iii) the expression levels of regulatory RNA species (including microRNAs and long non-coding RNAs) in both human and murine samples. Thus, several research groups worldwide, including us, have adopted one of these approaches to get further insights into CDDP resistance. Nonetheless, the potential of these methods is intrinsically limited by the frequent lack of correlation between copy number or mRNA/microRNA expression levels and phenotype, calling for robust rounds of functional validation.<sup><xref ref-type="bibr" rid="bib205">205</xref></sup> Recently, along with the evolution of mass spectrometry and the development of high-throughput techniques for the study of post-translational protein modifications (including, but not limited to, phosphorylation and acetylation),<sup><xref ref-type="bibr" rid="bib206">206</xref>, <xref ref-type="bibr" rid="bib207">207</xref>, <xref ref-type="bibr" rid="bib208">208</xref>, <xref ref-type="bibr" rid="bib209">209</xref></sup> attention has been refocused to proteomic/interactomic approaches as well as to the identification of novel signal transduction cascades that underpin CDDP resistance. In addition, great enthusiasm has been generated by the possibility to sequence the whole genome of neoplastic lesions, as first achieved for acute myeloid leukemia and quickly thereafter for various other malignancies.<sup><xref ref-type="bibr" rid="bib210">210</xref>, <xref ref-type="bibr" rid="bib211">211</xref>, <xref ref-type="bibr" rid="bib212">212</xref>, <xref ref-type="bibr" rid="bib213">213</xref>, <xref ref-type="bibr" rid="bib214">214</xref></sup> Further increasing the potential of this approach, Murtaza <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib215">215</xref></sup> have just demonstrated that advanced solid tumors can be sequenced starting from DNA molecules released by malignant cells into the plasma, <italic>de facto</italic> constituting a non-invasive liquid biopsy. Again, although these approaches can undoubtedly improve our understanding of CDDP resistance, caution should be taken while interpreting sequencing data in the absence of functional validation.</p><p>Several factors have recently been revealed or confirmed to contribute to CDDP resistance as a result of genomic, methylomic, transcriptomic and proteomic studies (<xref ref-type="supplementary-material" rid="sup1">Supplementary Table 1</xref>). Using CGH arrays, Cui <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib216">216</xref></sup> identified an interleukin-7 (IL-7)-dependent autocrine loop specifically activated in glioma cells that have lost their sensitivity to CDDP. By means of an integrated approach involving CGH arrays and transcriptomic studies, Jiffar <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib218">218</xref></sup> demonstrated that head and neck squamous cell carcinomas (HNSCCs) can become resistant to CDDP along with the loss of KiSS-1 metastasis-suppressor (KISS1), a G protein-coupled receptor ligand that also mediates CDDP-independent oncosuppressive functions.<sup><xref ref-type="bibr" rid="bib217">217</xref>, <xref ref-type="bibr" rid="bib218">218</xref></sup> By comparing the methylome of CDDP-sensitive and CDDP-resistant isogenic ovarian cancer cells, Yu <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib219">219</xref></sup> found that the latter exhibit not only a global decrease in the methylation of CpG islands but also specific alterations including the hypomethylation (which is generally associated with increased gene expression) of protein tyrosine kinase 6 (<italic>PTK6</italic>), coding for a non-receptor tyrosine kinase with prominent pro-survival functions; protein kinase C<italic>ɛ</italic> (<italic>PRKCE</italic>), encoding a Ca<sup>2+</sup>- and diacylglycerol-activated serine/threonine kinase, and BCL-2-like 1 (<italic>BCL2L1</italic>), coding for BCL-X<sub>L</sub>.<sup><xref ref-type="bibr" rid="bib219">219</xref></sup> By means of a systems biology approach comprising a methylomic and a transcriptomic component, Zeller <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib220">220</xref></sup> identified a set of nine genes that are hypermethylated (resulting in decreased transcription) both in several, independent CDDP-resistant derivatives of an ovarian carcinoma cell line (i.e., A2780 cells), and in clinical samples from ovarian carcinoma patients relapsing upon platinum-based chemotherapy. Besides <italic>MLH1</italic>, which is often mutated or downregulated in the context of CDDP resistance,<sup><xref ref-type="bibr" rid="bib126">126</xref>, <xref ref-type="bibr" rid="bib127">127</xref>, <xref ref-type="bibr" rid="bib128">128</xref>, <xref ref-type="bibr" rid="bib129">129</xref></sup> these genes include Rho GDP dissociation inhibitor <italic>β</italic> beta (<italic>ARHGDIB</italic>), armadillo repeat containing, X-linked 2 (<italic>ARMCX2</italic>), collagen, type I, <italic>α</italic>1 (<italic>COL1A1</italic>), filamin A<italic>α</italic> (<italic>FLNA</italic>) filamin C<italic>γ</italic> (<italic>FLNC</italic>), mesoderm-specific transcript (<italic>MEST</italic>), neurotensin (<italic>NTS</italic>) and proteasome (prosome, macropain) subunit, <italic>β</italic> type, 9 (<italic>PSMB9</italic>), pointing to the existence of hitherto unexplored mechanisms whereby malignant cells can lose their sensitivity to CDDP.<sup><xref ref-type="bibr" rid="bib220">220</xref></sup> Ivanova <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib221">221</xref></sup> applied a very similar experimental strategy to study gastric cancer, identifying bone morphogenetic protein 4 (BMP4) as an epigenetically regulated factor that underpins CDDP (but not oxaliplatin) resistance and exerts oncogenic functions (at least in this setting) by promoting the epithelial-to-mesenchymal transition (EMT). It remains unclear whether the oncogenic activity of BMP4, similar to that of IL-7, relies on autocrine signaling circuitries.</p><p>The profound implication of the DNA repair machinery and the BCL-2 protein family in CDDP resistance has been confirmed by a large number of recent transcriptomic studies.<sup><xref ref-type="bibr" rid="bib118">118</xref>, <xref ref-type="bibr" rid="bib124">124</xref>, <xref ref-type="bibr" rid="bib222">222</xref>, <xref ref-type="bibr" rid="bib223">223</xref>, <xref ref-type="bibr" rid="bib224">224</xref>, <xref ref-type="bibr" rid="bib225">225</xref>, <xref ref-type="bibr" rid="bib226">226</xref></sup> However, none of these factors has yet been validated as a reliable clinical predictor of CDDP sensitivity.<sup><xref ref-type="bibr" rid="bib124">124</xref></sup> Alongside, the abundance of transcripts coding for several proteins that have no obvious links with CDDP-elicited signaling pathway has been correlated with clinical CDDP resistance. These factors include AKT1, eukaryotic translation initiation factor 4B (EIF4B) and ribosomal protein S6 (RPS6), defining a metabolic signature linked to the activity of mammalian target of rapamycin (mTOR);<sup><xref ref-type="bibr" rid="bib227">227</xref></sup> cytochrome P450, family 4, subfamily B, polypeptide 1 (CYP4B1), choline/ethanolamine phosphotransferase 1 (CEPT1) and charged multivesicular body protein 4A (CHMP4A),<sup><xref ref-type="bibr" rid="bib228">228</xref></sup> as well as several proteins implicated in the EMT.<sup><xref ref-type="bibr" rid="bib229">229</xref></sup> However, whether the EMT triggers a specific pathway of CDDP resistance or these observations rather reflect the high number of genetic and epigenetic alterations that characterize advanced neoplastic lesions (underpinning their aggressiveness and chemoresistance) remains to be determined. Furthermore, by analyzing HNSCC biopsies with whole-genome microarrays and quantitative reverse transcriptase PCR cards, Tomkiewicz <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib230">230</xref></sup> delineated a 10-gene signature that predicts the response of HNSCC patients to CDDP/5-FU-based induction chemotherapy. As it stands, most of these genes have not been previously implicated in CDDP resistance, although some of them code for factors that have a role in the cytoprotective response to redox stress, such as DnaJ (Hsp40) homolog, subfamily A, member 1 (<italic>DNAJA1</italic>) and thioredoxin domain containing 9 (<italic>TXNDC9</italic>).<sup><xref ref-type="bibr" rid="bib230">230</xref></sup></p><p>By comparing the transcriptomic profile of NSCLC A549 cells exposed to cytotoxic doses of CDDP, cadmium dichloride (CdCl<sub>2</sub>, an environmental pollutant that triggers oxidative stress-dependent apoptosis) and C<sub>2</sub>-ceramide (a plasma membrane permeant ceramide with mitochondriotoxic effects), we have recently demonstrated that CDDP elicits signaling cascades (encompassing both pro-survival and pro-death pathways) that are for the most part ‘private', that is, they manifest limited overlap with the molecular mechanisms set in motion by other inducers of mitochondrial apoptosis.<sup><xref ref-type="bibr" rid="bib231">231</xref></sup> Along similar lines, by studying the microRNAome of A549 cells succumbing to CDDP, CdCl<sub>2</sub> or C<sub>2</sub>-ceramide, we identified miR-181a and miR-630 as functional components of the molecular mechanisms that underpin CDDP toxicity and the general cytoprotective response of A549 cells to stress, respectively.<sup><xref ref-type="bibr" rid="bib232">232</xref></sup> On a similar note, several research groups have recently investigated the microRNAomic profile of CDDP-sensitive <italic>versus</italic> CDDP-resistant cancer cell lines of various origin, including glioblastoma,<sup><xref ref-type="bibr" rid="bib233">233</xref></sup> tongue squamous cell carcinoma (TSCC),<sup><xref ref-type="bibr" rid="bib234">234</xref></sup> NSCLC,<sup><xref ref-type="bibr" rid="bib235">235</xref>, <xref ref-type="bibr" rid="bib236">236</xref>, <xref ref-type="bibr" rid="bib237">237</xref>, <xref ref-type="bibr" rid="bib238">238</xref></sup> hepatocellular carcinoma (HCC)<sup><xref ref-type="bibr" rid="bib239">239</xref></sup> and ovarian carcinoma.<sup><xref ref-type="bibr" rid="bib240">240</xref>, <xref ref-type="bibr" rid="bib241">241</xref></sup> Several of these studies identified the downregulation of microRNAs that inhibit the expression of anti-apoptotic BCL-2-like proteins (e.g., miR-135 and miR-497) as a prominent mechanism of CDDP resistance.<sup><xref ref-type="bibr" rid="bib235">235</xref>, <xref ref-type="bibr" rid="bib236">236</xref></sup> In addition, a decrease in the sensitivity of cancer cells to the cytostatic/cytotoxic effects of CDDP has been associated with the upregulation of microRNAs that target the major oncosuppressive factor phosphatase and tensin homolog (PTEN), such as miR-130a and miR-93,<sup><xref ref-type="bibr" rid="bib240">240</xref>, <xref ref-type="bibr" rid="bib241">241</xref></sup> and ERCC1, like miR-138,<sup><xref ref-type="bibr" rid="bib237">237</xref></sup> as well as with the downregulation of microRNAs that normally limit the expression of cell cycle-associated proteins such as let-7b.<sup><xref ref-type="bibr" rid="bib233">233</xref></sup> Similarly, CDDP resistance in cultured A549 cells has been correlated with the downregulation of a long non-coding RNA (AK126698) that inhibits WNT/<italic>β</italic>-catenin signaling.<sup><xref ref-type="bibr" rid="bib238">238</xref></sup></p><p>At odds with our observations, elevated expression levels of miR-181a have been associated with a decreased (rather than increased) sensitivity of cultured HCC cells to multiple antineoplastic agents, including CDDP.<sup><xref ref-type="bibr" rid="bib239">239</xref></sup> Such an apparent discrepancy may originate from the experimental systems employed (i.e., acute response to CDDP in NSCLC cells <italic>versus</italic> stably acquired resistance in HCC cells) or reflect a context-dependent role of miR-181a. This said, elevated expression levels of miR-181 species (in the context of a 58-component microRNA signature) have been shown to predict the response of gastric carcinoma patients to CDDP/5-FU-based chemotherapy.<sup><xref ref-type="bibr" rid="bib242">242</xref></sup> The precise elucidation of the molecular targets of miR-181 may provide important insights this issue. In another clinical study, the upregulation of miR-135b and miR-145 in response to trimodal therapy (concurrent CDDP, irinotecan and irradiation, followed by surgery) has been associated with poor disease-free survival (DFS) among esophageal carcinoma patients,<sup><xref ref-type="bibr" rid="bib243">243</xref></sup> but the molecular mechanisms underpinning these observations have not been further investigated. Interestingly, microRNAomic studies also implicate the EMT in CDDP resistance. In particular, miR-200b and miR-15b (which are downregulated in CDDP-resistant TSCC cells) turned out to actively inhibit the EMT (hence exerting oncosuppressive effects) by targeting the polycomb ring finger oncogenic factor BMI1.<sup><xref ref-type="bibr" rid="bib234">234</xref></sup> In line with this notion, reduced intratumoral levels of miR-200b or miR-15b have been associated with clinical CDDP resistance and poor survival in a cohort of TSCC patients.<sup><xref ref-type="bibr" rid="bib234">234</xref></sup> Of note, the expression of several microRNAs and proteins that contribute to CDDP resistance is under the control of epigenetic mechanisms, including DNA methylation and histone acetylation.<sup><xref ref-type="bibr" rid="bib244">244</xref>, <xref ref-type="bibr" rid="bib245">245</xref>, <xref ref-type="bibr" rid="bib246">246</xref>, <xref ref-type="bibr" rid="bib247">247</xref></sup> This raises the intriguing possibility that pharmacological inhibitors of DNA methyltransferases and histone deacetylases, some of which are currently approved by international regulatory agencies for use in cancer patients, may limit CDDP resistance at least in part by modulating the abundance of specific microRNAs.<sup><xref ref-type="bibr" rid="bib247">247</xref>, <xref ref-type="bibr" rid="bib248">248</xref>, <xref ref-type="bibr" rid="bib249">249</xref>, <xref ref-type="bibr" rid="bib250">250</xref>, <xref ref-type="bibr" rid="bib251">251</xref>, <xref ref-type="bibr" rid="bib252">252</xref></sup> Robust experimental evidence in support of this hypothesis is lacking.</p><p>Various aspects of CDDP resistance have been uncovered by proteomic approaches. By combining quantitative proteomics with interaction network analyses, Chavez <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib253">253</xref></sup> demonstrated that the levels of no less than 374 proteins are altered in CDDP-resistant (as compared with wild-type, CDDP-sensitive) cervical carcinoma HeLa cells, including various components of energy-producing metabolic pathways as well as proteins involved in DNA repair and other stress response mechanisms. Zeng <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib254">254</xref></sup> found CDDP-insensitive NSCLC A549 cells to differ from their CDDP-susceptible counterparts in the expression levels of 9 proteins, including parkinson protein 7 (PARK7, best known as DJ-1), a transcription-modulatory and antioxidant factor implicated in the development of familiar Parkinson disease. These findings had an important clinical correlate, as elevated amounts of DJ-1 turned out to predict poor disease outcome in a cohort of 67 locally advanced NSCLC patients.<sup><xref ref-type="bibr" rid="bib254">254</xref></sup> Along similar lines, Roesch <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib255">255</xref></sup> demonstrated that melanoma cells exposed for long periods to suboptimal CDDP concentrations not only express increased levels of the histone demethylase Jumonji, AT-rich interactive domain 1 (JARID1) but also contain increased amounts of several enzymes implicated in mitochondrial respiration. Importantly, inhibition of the mitochondrial respiratory chain appears to prevent the accumulation of these slowly proliferating CDDP-insensitive cells, delineating a strategy for the selective elimination of malignant cell clones that initially resist CDDP-based chemotherapy.<sup><xref ref-type="bibr" rid="bib255">255</xref></sup> Accordingly, the response of esophageal adenocarcinoma patients to neo-adjuvant CDDP-based chemotherapy correlates with mitochondrial defects provoked by the loss of specific cytochrome c oxidase (COX) subunits.<sup><xref ref-type="bibr" rid="bib256">256</xref></sup> On a slightly different note, Vasko <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib257">257</xref></sup> investigated the acute proteomic alterations caused by therapeutic concentrations of CDDP in renal cell carcinoma cells. In this context, CDDP-treated cells were found to express increased levels of multiple cytoskeletal proteins, molecular chaperones of the HSP family and glycolytic enzymes.<sup><xref ref-type="bibr" rid="bib257">257</xref></sup> Taken together, these observations suggest that cancer cells acutely exposed to CDDP might temporarily rely on glycolysis as a source of energy (presumably reflecting the mitochondriotoxic effects of cytoplasmic CDDP), whereas the acquisition of stable CDDP resistance might require a robust respiratory activity.<sup><xref ref-type="bibr" rid="bib255">255</xref>, <xref ref-type="bibr" rid="bib256">256</xref>, <xref ref-type="bibr" rid="bib257">257</xref></sup> At least in part, this is at odds with our recent findings, indicating that CDDP resistance can be mediated by the activation of a PPARGC1B-dependent signaling pathway that is elicited by respiratory chain defects but does not depend on mitochondrial biogenesis.<sup><xref ref-type="bibr" rid="bib150">150</xref></sup> Thus, the precise contribution of glycolysis and mitochondrial respiration to the development of CDDP resistance remains to be clarified.</p><p>As an alternative to conventional whole-cell approaches, proteomic studies to elucidate CDDP resistance have been performed on enriched subcellular compartments (e.g., nuclei, mitochondria),<sup><xref ref-type="bibr" rid="bib258">258</xref>, <xref ref-type="bibr" rid="bib259">259</xref>, <xref ref-type="bibr" rid="bib260">260</xref></sup> purified components known to participate in CDDP-elicited signaling pathways (e.g., immobilized CDDP, Y-box binding protein 1),<sup><xref ref-type="bibr" rid="bib149">149</xref>, <xref ref-type="bibr" rid="bib261">261</xref></sup> as well as on serum samples from cancer patients.<sup><xref ref-type="bibr" rid="bib262">262</xref>, <xref ref-type="bibr" rid="bib263">263</xref></sup> The latter approach allowed for the identification of <italic>α</italic>1-antitripsin (a circulating protease inhibitor with anti-inflammatory functions) and S100A9 (a Ca<sup>2+</sup>-binding protein that exerts immunomodulatory effects) as possible biomarkers of clinical CDDP resistance.<sup><xref ref-type="bibr" rid="bib262">262</xref>, <xref ref-type="bibr" rid="bib263">263</xref></sup> Moreover, CDDP resistance has been associated with immunopeptidomic alterations, that is, changes in the composition and abundance of peptides presented on the cell surface in complex with MHC molecules.<sup><xref ref-type="bibr" rid="bib260">260</xref></sup> This is particularly important in view of the facts that (i) several anticancer regimens operate by eliciting or boosting anticancer immunity, some of them by altering the immunopeptidome of malignant cells<sup><xref ref-type="bibr" rid="bib264">264</xref>, <xref ref-type="bibr" rid="bib265">265</xref></sup> and that (ii) CDDP is generally considered as a non-immunogenic anticancer agent.<sup><xref ref-type="bibr" rid="bib24">24</xref>, <xref ref-type="bibr" rid="bib25">25</xref></sup> Thus, it is tempting to speculate that CDDP resistance might involve specific changes in the immunopeptidome of neoplastic cells as well as in the tumor microenvironment that prevent the activation of anticancer immune responses. Formal evidence in support of this hypothesis is missing.</p></sec><sec><title>Large-scale silencing approaches and functional screenings</title><p>In the mid 2000s, key technological advances have allowed researchers to tackle CDDP resistance with large-scale functional/empirical approaches, as opposed to high-throughput observational studies followed by low-throughput functional validation (such as the genomic, methylomic, transcriptomic and proteomic approaches described above). These developments include (but perhaps are not limited to): (i) the availability of the first genome-wide siRNA sets, at least theoretically permitting the downregulation of each mRNA encoded by the human or murine genome;<sup><xref ref-type="bibr" rid="bib266">266</xref>, <xref ref-type="bibr" rid="bib267">267</xref></sup> (ii) the explosion of combinatorial chemistry, allowing for the generation of huge libraries of compounds for investigational purposes<sup><xref ref-type="bibr" rid="bib268">268</xref>, <xref ref-type="bibr" rid="bib269">269</xref></sup> and (iii) the rapid diffusion of fully robotized platforms compatible with the sterile handling of 96- and 384-well plates.<sup><xref ref-type="bibr" rid="bib270">270</xref>, <xref ref-type="bibr" rid="bib271">271</xref></sup> Thus, along with the establishment of reproducible and cost-efficient workflows, large-scale silencing approaches and ample chemical screenings have been undertaken by several groups worldwide, providing profound insights into the phenomenon of CDDP resistance.<sup><xref ref-type="bibr" rid="bib231">231</xref>, <xref ref-type="bibr" rid="bib272">272</xref>, <xref ref-type="bibr" rid="bib273">273</xref>, <xref ref-type="bibr" rid="bib274">274</xref>, <xref ref-type="bibr" rid="bib275">275</xref>, <xref ref-type="bibr" rid="bib276">276</xref>, <xref ref-type="bibr" rid="bib277">277</xref></sup> It should be noted that these functional/empirical approaches are not exempted from validation. Rather, primary hits must be confirmed upon (i) the exclusion of putative off-target effects and the establishment of a robust cause–effect relationship between the downregulation of a specific protein and CDDP resistance (possibly coupled to the elucidation of the underlying mechanisms) or (ii) the precise identification of the molecular target(s) through which a given chemical alters the sensitivity of cancer cells to CDDP (and again the clarification of mechanistic aspects of this phenomenon). Similar to the genomic, transcriptomic, methylomic and proteomic approaches described above, these functional/empiric approaches rely on homotypic experimental settings, mainly cultured cancer cells, <italic>de facto</italic> overlooking the notion that CDDP resistance (at least in some settings) might originate from alterations of the tumor microenvironment or systemic defects (see below). Approximately in the same period, investigators have attempted to elucidate the mechanisms that limit the sensitivity of malignant cells to CDDP by taking advantage of well-established, genetically tractable models that would be compatible with ample knockout strategies, such as <italic>Saccharomyces cerevisiae</italic>, <italic>Schizosaccharomyces pombe</italic> and <italic>Dictyostelium discoideum</italic>.<sup><xref ref-type="bibr" rid="bib89">89</xref>, <xref ref-type="bibr" rid="bib231">231</xref>, <xref ref-type="bibr" rid="bib278">278</xref>, <xref ref-type="bibr" rid="bib279">279</xref>, <xref ref-type="bibr" rid="bib280">280</xref>, <xref ref-type="bibr" rid="bib281">281</xref></sup> Although these genetic approaches are cost-efficient and straightforward, hits must be subjected to multiple, intense rounds of cross-species functional validation.</p><p>We have been working intensively along these lines to obtain clinically relevant insights into CDDP resistance. As a result of a genome-wide siRNA screening approach, we identified the metabolism of vitamin B6 as a central regulator of the response of cancer cells to a wide array of nutritional, physical and chemical stress conditions, including the administration of CDDP.<sup><xref ref-type="bibr" rid="bib272">272</xref>, <xref ref-type="bibr" rid="bib282">282</xref></sup> In particular, we found that the cytotoxic response of a large panel of cancer cells to stress is significantly exacerbated in the presence of a cell permeant B6 vitamer, pyridoxine. Such an effect was only observed when cells expressed pyridoxal kinase (PDXK), the enzyme that generates the bioactive form of vitamin B6 (pyridoxal-5-phosphate). In line with this notion, the downregulation of PDXK conferred a significant degree of protection from stress to cancer cells, while that of pyridoxal phosphatase (PDXP), the enzyme that degrades bioactive vitamin B6, caused a robust increase in the cytotoxicity of several stimuli.<sup><xref ref-type="bibr" rid="bib272">272</xref></sup> Importantly, NSCLC patients (from two distinct cohorts, one from Europe and one from North America) bearing lesions that expressed high levels of PDXK had an improved disease-free and overall survival (OS) than individuals affected by tumors with low PDXK levels, irrespective of therapy.<sup><xref ref-type="bibr" rid="bib272">272</xref></sup> Of note, the prognostic value of the vitamin B6 metabolism among NSCLC patients was clear when PDXK levels were quantified by immunohistochemistry (IHC) in malignant cells, but neither when the adjacent, non-malignant lung tissue was analyzed (implying that the effect of vitamin B6 on disease progression originates in the tumor) nor when the amount of the PDXK-coding mRNA was assessed in tumor biopsies (perhaps suggesting that PDXK is subjected to a relevant degree of post-transcriptional regulation).<sup><xref ref-type="bibr" rid="bib272">272</xref></sup> Although the precise molecular mechanisms whereby vitamin B6 sensitizes malignant cells to adverse conditions remain unclear, we found that the administration of pyridoxine (i) facilitates the establishment of oxidative stress (presumably explaining the influence of vitamin B6 on tumor progression)<sup><xref ref-type="bibr" rid="bib272">272</xref></sup> and (ii) promotes the intracellular accumulation of CDDP (at least in part accounting for the ability of vitamin B6 to promote the cytotoxicity of CDDP, <italic>in vitro</italic> and <italic>in vivo</italic>).<sup><xref ref-type="bibr" rid="bib273">273</xref></sup> Both these effects were strictly dependent on the presence of PDXK, implying that they both are mediated by pyridoxal-5-phosphate.<sup><xref ref-type="bibr" rid="bib272">272</xref>, <xref ref-type="bibr" rid="bib273">273</xref>, <xref ref-type="bibr" rid="bib282">282</xref></sup> Of note, the same study led us to identify 84 additional factors that influence the response of NSCLC to CDDP, including lipase, hepatic (LIPC).<sup><xref ref-type="bibr" rid="bib283">283</xref></sup> Similar to those of PDXK, the intratumoral levels of LIPC turned out to positively correlate with disease outcome (independent of several other prognostic factors, including PDXK expression) in two distinct cohorts of NSCLC patients.<sup><xref ref-type="bibr" rid="bib283">283</xref></sup> Moreover, in one of these relatively small cohorts, LIPC expression levels tended to have a predictive (as opposed to merely prognostic) value.<sup><xref ref-type="bibr" rid="bib283">283</xref></sup> Thus, although validation in large patient cohorts is still pending, LIPC expression levels may constitute a biomarker that allows for the identification of patients who obtain a true clinical benefit from the administration of platinum-based chemotherapy. This said, the molecular mechanisms through which LIPC influences tumor progression (and perhaps response to chemotherapy) remain obscure.</p><p>A few other groups have undertaken global silencing approaches to discover novel factors involved in CDDP resistance. For instance, Ho <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib277">277</xref></sup> found that the GTPase RAS homolog family member J (RHOJ) and p21 protein (CDC42/RAC)-activated kinase 1 (PAK1) render melanoma cells resistant to DNA-damaging agents (including dacarbazine and CDDP) by uncoupling ATR from its downstream effectors, resulting in the expression of the survival gene SRY (sex determining region Y)-box 10 (<italic>SOX10</italic>). By focusing this strategy on lipid and protein kinases, Guerreiro <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib284">284</xref></sup> identified a set of six factors involved in the decreased sensitivity of medulloblastoma cells to CDDP, including ATR, membrane protein, palmitoylated 2 (MPP2), phosphatidylinositol 4-kinase, catalytic, <italic>α</italic> (PI4KA), phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit <italic>γ</italic> (PIK3CG), STE20-related kinase adaptor <italic>α</italic> (STRADA, a pseudokinase also known as LYK5) and WNK lysine-deficient protein kinase 4 (WNK4). A kinome-wide siRNA screen allowed Salm <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib276">276</xref></sup> to identify fibroblast growth factor receptor 2 (FGFR2) as an important determinant of CDDP resistance in neuroblastoma. FGFR2 turned out to decrease the sensitivity of neuroblastoma cells to CDDP via an autocrine loop promoting the expression of BCL-2 and BCL-X<sub>L</sub>. Moreover, the expression levels of FGFR2 were shown to have a clinical relevance, as they correlated with the amplification of <italic>v-myc</italic> avian myelocytomatosis viral oncogene neuroblastoma-derived homolog (<italic>MYCN</italic>) and advanced disease stage.<sup><xref ref-type="bibr" rid="bib276">276</xref></sup> Of note, silencing approaches can also be implemented by means of microRNA mimics. By screening a panel of these reagents, Pouliot <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib285">285</xref></sup> demonstrated that several microRNAs of the miR-15 family, including miR-15a, miR-15b, miR-16, miR-16-1* and miR-424*, alter the sensitivity of epidermoid carcinoma cells to CDDP as they regulate the expression of cell cycle-associated kinases.</p><p>Large chemical libraries have been screened for the presence of compounds that may increase the susceptibility of malignant cells to the cytostatic/cytotoxic effects of CDDP. Using this approach, Chen <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib275">275</xref></sup> identified pimozide and GW7647, two distinct inhibitors of the deubiquitinase complex assembled by ubiquitin specific peptidase 1 (USP1) and WD repeat domain 48 (WDR48, also known as UAF1), as putative chemosensitizers in NSCLC cells. As the USP1/UAF1 complex is involved in TLS, pimozide and GW7647 may operate by limiting the ability of cancer cells to bypass CDDP-induced DNA lesions. By screening a validated library of kinase inhibitors, Wong <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib286">286</xref></sup> demonstrated that the inhibition of several signal transducers including AKT1, mTOR, NF-<italic>κ</italic>B, transforming growth factor <italic>β</italic> receptor 1 (TGFBR1), phosphoinositide-3-kinase (PI3K) and various MAPKs sensitizes basal-like breast carcinoma cells to the toxic effects of CDDP. Specifically, the mTOR inhibitor rapamycin was shown to synergize with CDDP in the killing of basal-like MDA-MB-468, MDA-MB-231 and HCC1937 cells, but not luminal-like T47D or MCF-7 cells, owing to the induction of the p53-related protein p73.<sup><xref ref-type="bibr" rid="bib286">286</xref></sup> Jacquemont <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib274">274</xref></sup> tested >16 000 compounds for their ability to inhibit the formation of DNA damage foci triggered by irradiation or CDDP, identifying a dozen molecules that sensitize ovarian cancer cells to the cytotoxic effects of the latter. These molecules include several inhibitors of the Fanconi anemia (FA) DNA repair pathway (which coordinates HR and TLS for the repair of interstrand crosslinks) and indeed were confirmed to exacerbate the cytostatic/cytotoxic potential of CDDP in FA-proficient but not in FA-deficient ovarian cancer cells. Finally, Garnett <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib287">287</xref></sup> recently undertook a large screen to identify genes associated with the cellular responses to most anticancer agents available to date. To this aim, 130 drugs currently approved by regulatory agencies for use in cancer patients or under clinical development were tested on several hundred cancer cell lines, representing much of the tissue-type and genetic diversity of human tumors. This systematic screening approach generated several unexpected findings, including the extremely high sensitivity to both PARP inhibitors and CDDP of Ewing's sarcoma cells harboring a translocation that involves EWS RNA-binding protein 1 (<italic>EWSR1</italic>) and Fli-1 proto-oncogene, ETS transcription factor (<italic>FLI1</italic>).<sup><xref ref-type="bibr" rid="bib287">287</xref></sup></p><p>Functional screenings recently performed in genetically tractable organisms have also unveiled various aspects of CDDP resistance. For instance, by screening the clonogenic potential of a collection of <italic>S. cerevisiae</italic> mutants exposed to an overtly toxic amount of CDDP, we demonstrated that the molecular cascades elicited by CDDP, CdCl<sub>2</sub> and C<sub>2</sub>-ceramide in yeast exhibit very limited overlaps.<sup><xref ref-type="bibr" rid="bib231">231</xref></sup> Indeed, none of the <italic>S. cerevisiae</italic> mutants tested was protected from the cytostatic/cytotoxic potential of all these compounds. Of note, <italic>Δpor2</italic> cells, lacking one isoform of the yeast ortholog of human VDAC1, turned out to be specifically protected against CDDP cytotoxicity, indicating that the molecular mechanisms that underlie CDDP resistance are phylogenetically conserved.<sup><xref ref-type="bibr" rid="bib231">231</xref></sup> Upon the development of a high-resolution high-throughput screening (HTS) platform, Sletta <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib281">281</xref></sup> tested the response of >1400 <italic>S. cerevisiae</italic> deletion mutants to three distinct DNA-damaging agents, namely, methyl methanesulphonate, 5-FU and CDDP, identifying MAPK7 (also known as ERK5) as an evolutionarily ancient regulator of the DNA damage response that also operates in human cells. Using 2359 non-essential haploid deletion mutants of the fission yeast <italic>S. pombe</italic>, Gatti <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib280">280</xref></sup> identified no less than 13 distinct gene products involved in the ubiquitin-proteasome system whose absence increases (3 proteins) or decreases (10 proteins) CDDP sensitivity. Although these authors did not validate their findings in mammalian systems, we and others confirmed the implication of the proteasome in the response of human cells to CDDP.<sup><xref ref-type="bibr" rid="bib220">220</xref>, <xref ref-type="bibr" rid="bib272">272</xref></sup></p></sec><sec><title>Multiplex genotyping studies</title><p>During the last decade, dozens of studies have been carried out to determine whether SNPs affecting one or more genetic loci would influence the natural course of multiple neoplasms (leading to the identification of prognostic biomarkers) or the propensity of neoplastic lesions to respond to specific therapeutic regimens, including CDDP-based chemotherapy (resulting in the characterization of predictive biomarkers).<sup><xref ref-type="bibr" rid="bib288">288</xref>, <xref ref-type="bibr" rid="bib289">289</xref>, <xref ref-type="bibr" rid="bib290">290</xref>, <xref ref-type="bibr" rid="bib291">291</xref></sup> This approach has obvious clinical implications because it may lead to the identification of patient subgroups that will benefit from treatment, and hence allow for the implementation of personalized medicine.<sup><xref ref-type="bibr" rid="bib292">292</xref></sup> Moreover, the identification of genetic backgrounds that influence the antineoplastic activity of CDDP would have one major advantage as compared with most strategies for the elucidation of resistance discussed above: it would intrinsically consider all possible cancer cell-extrinsic factors that may impact on this phenomenon, irrespective of whether they have previously been described or not. However, until recently, genotyping studies could only focus on SNPs affecting one (or a few) protein(s) at the same time, owing to technical limitations. Thus, near-to-invariably, these approaches would study SNPs known or expected to influence cellular or organismal processes linked to CDDP sensitivity, such as CDDP extrusion (e.g., SNPs affecting ABCC2), DNA damage-elicited signal transduction (e.g., SNPs affecting ERCC1), apoptosis (e.g., SNPs affecting caspases) or immune responses (e.g., SNPs affecting cytokines or their receptors).<sup><xref ref-type="bibr" rid="bib293">293</xref>, <xref ref-type="bibr" rid="bib294">294</xref>, <xref ref-type="bibr" rid="bib295">295</xref>, <xref ref-type="bibr" rid="bib296">296</xref>, <xref ref-type="bibr" rid="bib297">297</xref>, <xref ref-type="bibr" rid="bib298">298</xref></sup> This limitation has nowadays been circumvented by the introduction of technical platforms that allow for the simultaneous determination of up to 384 different SNPs in one single assay.<sup><xref ref-type="bibr" rid="bib299">299</xref>, <xref ref-type="bibr" rid="bib300">300</xref>, <xref ref-type="bibr" rid="bib301">301</xref></sup></p><p>A few genotyping studies of this type have already been performed to obtain insights into the organismal aspects of CDDP resistance. Tan <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib302">302</xref></sup> reported that two SNPs affecting the expression levels of death-associated protein kinase 3 (DAPK3) and methyltransferase like 6 (METTL6) influenced disease outcome in 222 small cell lung carcinoma and 961 NSCLC patients treated with platinum-based therapy. Accordingly, the knockdown of DAPK3 and METTL6 was shown to significantly decrease CDDP sensitivity in lung carcinoma cells.<sup><xref ref-type="bibr" rid="bib302">302</xref></sup> By adopting a similar approach, Wheeler <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib303">303</xref></sup> tested the association between 2 million SNPs and the response of lymphoblastoid cell lines (LCLs) derived from 83 individuals of African American descent to cytarabine, 5′-deoxyfluorouridine, carboplatin and CDDP. This study led to the identification of 41 genes that putatively influence the response of African Americans to CDDP-based chemotherapy. Notably, the set of SNPs associated with the sensitivity of LCLs to CDDP exhibited some degree of overlap with that linked to carboplatin susceptibility, reinforcing the notion that platinum derivatives activate similar, but not identical, signal transduction cascades.<sup><xref ref-type="bibr" rid="bib303">303</xref></sup> More recently, the same authors expanded their analysis to a total of 608 LCLs and >3 million SNPs, reporting a robust association between CDDP susceptibility and a SNP upstream of keratin 16 pseudogene 2 (<italic>KRT16P2</italic>) as well as a link between the sensitivity of LCLs to CDDP and SNPs affecting <italic>BCL2</italic>, <italic>ERCC2</italic>, <italic>ERCC6</italic>, glutathione S-transferase <italic>μ</italic>1 (<italic>GSTM1</italic>) and glutathione S-transferase <italic>θ</italic>1 (<italic>GSTT1</italic>).<sup><xref ref-type="bibr" rid="bib304">304</xref></sup> Li <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib305">305</xref></sup> analyzed the association between 894 SNPs affecting 70 genes involved in glutathione metabolism, DNA repair, cell cycle and epidermal growth factor receptor (EGFR) signaling and disease outcome among 1076 NSCLC patients treated with various platinum-based chemotherapeutic regimens. Globally, SNPs affecting glutathione synthetase (<italic>GSS</italic>) and mitogen-activated protein kinase kinase kinase 1 (<italic>MAP3K1</italic>) were linked to poor OS. Moreover, SNPs affecting <italic>MAP3K1</italic> turned out to negatively influence the OS of NSCLC patients treated with platinum derivatives plus a taxane, whereas SNPs in the <italic>v-raf-1</italic> murine leukemia viral oncogene homolog 1 (<italic>RAF1</italic>) had an opposite effect on the OS of this patient subgroup. Along similar lines, SNPs involving <italic>RAF1</italic> (as well as glutathione peroxidase 5, <italic>GPX5</italic>) were associated with improved OS among patients receiving platinum derivatives plus gemcitabine. Conversely, SNPs affecting <italic>GPX7</italic> and neuroblastoma RAS viral (<italic>v-ras</italic>) oncogene homolog (<italic>NRAS</italic>) had a negative influence on OS in these individuals.<sup><xref ref-type="bibr" rid="bib305">305</xref></sup> Wu <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib306">306</xref></sup> studied the influence of 307 260 distinct SNPs on the survival of three distinct cohorts of (327, 315 and 420) advanced-stage NSCLC patients who received platinum-based chemotherapy with or without irradiation, identifying a relatively reproducible (though not absolute) association between SNPs in chemokine-like receptor 1 (<italic>CMKLR1</italic>) and sortilin-related VPS10 domain containing receptor 2 (<italic>SORCS2</italic>) and poor OS. Along similar lines, Hu <italic>et al.</italic><sup><xref ref-type="bibr" rid="bib307">307</xref></sup> performed a fast-track genotyping study on three distinct cohorts of (307, 228 and 340) NSCLC patients receiving first-line platinum-based chemotherapy, finding an association between three SNPs (rs7629386 at 3p22.1, rs969088 at 5p14.1 and rs3850370 at 14q24.3) and poor OS as well as a link between two SNPs (rs41997 at 7q31.31 and rs12000445 at 9p21.3) and improved OS. These studies and others of a similar type to come may provide significant insights into the organismal aspect of CDDP resistance.</p></sec></sec><sec><title>Concluding Remarks</title><p>Throughout the last 4 decades, several millions of cancer patients have been treated with CDDP-based chemo(radio)therapeutic regimens. Exception made for individuals bearing testicular germ cell tumors, most of these patients only obtained temporary clinical benefits, which were destined to vanish along with the progressive transition of malignant cells from a chemosensitive to a chemoresistant state. Thus, even though CDDP provokes moderate-to-severe adverse effects in a fraction of patients, the most prominent hurdle related to the use of CDDP in the clinical practice is posed by the elevated incidence of chemoresistance, be it innate or acquired. An intense wave of preclinical and clinical investigation aimed at developing strategies to restore the sensitivity of human neoplasms to the cytostatic/cytotoxic effects of CDDP has been initiated worldwide in the late 1970s. Reflecting the huge clinical and socioeconomic impact of CDDP resistance, such an investigational effort has not yet come to an end. Indeed, although several strategies have been devised to circumvent CDDP resistance in cancer patients, including (but not limited to) the use of CDDP in combination with targeted anticancer agents such as erlotinib (a pharmacological inhibitor of the tyrosine kinase activity of EGFR), trastuzumab (an EGFR-specific antibody) and bevacizumab (a vascular endothelial growth factor-blocking antibody), a majority of these combinatorial regimens failed to improve the therapeutic profile of CDDP in randomized clinical trials.<sup><xref ref-type="bibr" rid="bib308">308</xref>, <xref ref-type="bibr" rid="bib309">309</xref>, <xref ref-type="bibr" rid="bib310">310</xref></sup></p><sec><title>Past</title><p>Before the advent of high-content, high-throughput technologies, the elucidation of the molecular mechanisms underpinning the cytostatic/cytotoxic effects of CDDP has long been under the limelight. It was indeed tempting to accept the relatively straightforward assumptions that (i) CDDP would exert antineoplastic effects by binding one (or a few) molecular target(s), hence activating relatively simple signaling pathways, and (ii) that CDDP resistance would originate from the activation of mutually exclusive mechanisms. Starting with the early 1990s, the attention of molecular oncologists focused on the cellular factors that are responsible for the detection and repair of CDDP-elicited DNA lesions, and on the mechanisms whereby these systems transduce a lethal signal when damage is irreparable (on-target and post-target resistance). The increasingly more precise characterization of plasma membrane transporters that actively extrude various xenobiotics, including several members of the ATP-binding cassette (ABC) protein family,<sup><xref ref-type="bibr" rid="bib311">311</xref></sup> led to the hypothesis that CDDP resistance would mainly involve pre-target mechanisms. Such a hypothesis, however, was soon disconfirmed by findings from many groups indicating that the inhibition of ABC transporters does not suffice to reinstate CDDP sensitivity. In the early 2000s, the role of copper transporters in the uptake and extrusion of CDDP became clear, yet the experimental modulation of these systems also failed to completely abolish the insensitivity of some cancer cells to CDDP. Thus, the redundant and multifactorial nature of CDDP resistance has been established even before the advent of high-content, high-throughput technologies.</p></sec><sec><title>Present</title><p>The automation of functional screenings and the introduction of high-content experimental platforms have literally revolutionized the study of several biological phenomena, including CDDP resistance. The first high-content, high-throughput technologies (such as mRNA and CGH microarrays and mass spectrometry) have been available for more than a decade, but the true explosion of this area has occurred in the late 2000s, along with the commercialization of platforms such as automated fluorescence microscopes and the introduction of innovative protocols like deep sequencing. Several attempts have recently been made to harness these technologies for empirically resolving the clinical hurdle posed by CDDP resistance, with very promising results. In addition, increasingly more detailed insights into the complexity of the signal transduction pathways triggered by CDDP in cancer and normal cells have been obtained. Nonetheless, no chemosensitization strategies have yet been introduced into the clinical practice (though a few of them are currently being investigated in clinical settings).</p></sec><sec><title>Future</title><p>Accumulating evidence indicates that, contrarily to long-standing beliefs, the limited sensitivity of human neoplasms to CDDP may reflect not only cell-intrinsic but also cell-extrinsic alterations.<sup><xref ref-type="bibr" rid="bib24">24</xref>, <xref ref-type="bibr" rid="bib25">25</xref>, <xref ref-type="bibr" rid="bib312">312</xref>, <xref ref-type="bibr" rid="bib313">313</xref></sup> On one hand, CDDP appears to be much less effective than other chemotherapeutics, including oxaliplatin (in spite of their chemical resemblance), at inducing the immunogenic demise of cancer cells.<sup><xref ref-type="bibr" rid="bib314">314</xref>, <xref ref-type="bibr" rid="bib315">315</xref></sup> On the other hand, it has recently been shown that CDDP resistance is significantly influenced by non-transformed mesenchymal stem cells and other components of the tumor stroma, including proteins of the extracellular matrix and immunosuppressive cell populations.<sup><xref ref-type="bibr" rid="bib312">312</xref>, <xref ref-type="bibr" rid="bib313">313</xref>, <xref ref-type="bibr" rid="bib316">316</xref></sup> Until now, such a cell-extrinsic dimension of CDDP resistance was largely underestimated. We surmise that the application of high-content, high-throughput technologies to heterotypic experimental settings that involve not only malignant cells but also various other components of the tumor microenvironment (including endothelial, mesenchymal and immune cells) is the key for the development of efficient strategies to restore the sensitivity of multiple human neoplasms to CDDP. Along similar lines, we believe that the untargeted metabolomic profiling of CDDP-sensitive <italic>versus</italic> CDDP-resistant tumor models, an approach that only recently has begun to be applied to the study of chemoresistance,<sup><xref ref-type="bibr" rid="bib313">313</xref>, <xref ref-type="bibr" rid="bib317">317</xref>, <xref ref-type="bibr" rid="bib318">318</xref></sup> may yield important insights into this considerable clinical impediment.</p></sec></sec></body><back><ack><p>The authors are supported by the Ligue contre le Cancer (équipe labellisée); Agence National de la Recherche (ANR); Association pour la recherche sur le cancer (ARC); Associazione Italiana per la Ricerca sul Cancro (AIRC); Cancéropôle Ile-de-France; AXA Chair for Longevity Research; Institut National du Cancer (INCa); Fondation Bettencourt-Schueller; Fondation de France; Fondation pour la Recherche Médicale (FRM); the European Commission (ArtForce); the European Research Council (ERC); the LabEx Immuno-Oncology; the LabEx LERMIT; the SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE); the SIRIC Cancer Research and Personalized Medicine (CARPEM) and the Paris Alliance of Cancer Research Institutes (PACRI).</p></ack><glossary><def-list><def-item><term>5-FU</term><def><p>5-fluorouracil</p></def></def-item><def-item><term>ABCC2</term><def><p>ATP-binding cassette, subfamily C (CFTR/MRP), member 2</p></def></def-item><def-item><term>AKT1</term><def><p><italic>v-akt</italic> murine thymoma viral oncogene homolog 1</p></def></def-item><def-item><term>ATP7B</term><def><p>ATPase, Cu<sup>2+</sup> transporting, <italic>β</italic> polypeptide</p></def></def-item><def-item><term>BMP4</term><def><p>bone morphogenetic protein 4</p></def></def-item><def-item><term>BRCA1</term><def><p>breast cancer 1, early onset</p></def></def-item><def-item><term>BRCA2</term><def><p>breast cancer 2, early onset</p></def></def-item><def-item><term>CDDP</term><def><p><italic>cis</italic>-diamminedichloroplatinum(II)</p></def></def-item><def-item><term>CDK2</term><def><p>cyclin-dependent kinase 2</p></def></def-item><def-item><term>CTR1</term><def><p>copper transporter 1</p></def></def-item><def-item><term>DAPK3</term><def><p>death-associated protein kinase 3</p></def></def-item><def-item><term>DFS</term><def><p>disease-free survival</p></def></def-item><def-item><term>DSB</term><def><p>double-strand break</p></def></def-item><def-item><term>DYRK1B</term><def><p>dual-specificity Y-phosphorylation regulated kinase 1B</p></def></def-item><def-item><term>EGFR</term><def><p>epidermal growth factor receptor</p></def></def-item><def-item><term>EMT</term><def><p>epithelial-to-mesenchymal transition</p></def></def-item><def-item><term>ER</term><def><p>endoplasmic reticulum</p></def></def-item><def-item><term>ERCC1</term><def><p>excision repair cross-complementing rodent repair deficiency, complementation group 1</p></def></def-item><def-item><term>FA</term><def><p>Fanconi anemia</p></def></def-item><def-item><term>FDA</term><def><p>Food and Drug Administration</p></def></def-item><def-item><term>FGFR2</term><def><p>fibroblast growth factor receptor 2</p></def></def-item><def-item><term>GSH</term><def><p>reduced glutathione</p></def></def-item><def-item><term>GST</term><def><p>glutathione S-transferase</p></def></def-item><def-item><term>HCC</term><def><p>hepatocellular carcinoma</p></def></def-item><def-item><term>HNSCC</term><def><p>head and neck squamous cell carcinoma</p></def></def-item><def-item><term>HR</term><def><p>homologous recombination</p></def></def-item><def-item><term>HSP</term><def><p>heat-shock protein</p></def></def-item><def-item><term>HTS</term><def><p>high-throughput screening</p></def></def-item><def-item><term>IL-7</term><def><p>interleukin-7</p></def></def-item><def-item><term>LCL</term><def><p>lymphoblastoid cell line</p></def></def-item><def-item><term>LIPC</term><def><p>lipase, hepatic</p></def></def-item><def-item><term>MAPK</term><def><p>mitogen-activated protein kinase</p></def></def-item><def-item><term>MAP3K1</term><def><p>mitogen-activated protein kinase kinase kinase 1</p></def></def-item><def-item><term>METTL6</term><def><p>methyltransferase like 6</p></def></def-item><def-item><term>MLH1</term><def><p><italic>mutL</italic> homolog 1</p></def></def-item><def-item><term>MMR</term><def><p>mismatch repair</p></def></def-item><def-item><term>MOMP</term><def><p>mitochondrial outer membrane permeabilization</p></def></def-item><def-item><term>MSH2</term><def><p><italic>mutS</italic> homolog 2</p></def></def-item><def-item><term>mTOR</term><def><p>mammalian target of rapamycin</p></def></def-item><def-item><term>NER</term><def><p>nucleotide excision repair</p></def></def-item><def-item><term>NSCLC</term><def><p>non-small cell lung carcinoma</p></def></def-item><def-item><term>OS</term><def><p>overall survival</p></def></def-item><def-item><term>PARP1</term><def><p>poly(ADP-ribose) polymerase 1</p></def></def-item><def-item><term>PDXK</term><def><p>pyridoxal kinase</p></def></def-item><def-item><term>PPARGC1B</term><def><p>peroxisome proliferator-activated receptor <italic>γ</italic>, coactivator 1<italic>β</italic></p></def></def-item><def-item><term>PTPC</term><def><p>permeability transition pore complex</p></def></def-item><def-item><term>RAF1</term><def><p><italic>v-raf-1</italic> murine leukemia viral oncogene homolog 1</p></def></def-item><def-item><term>ROS</term><def><p>reactive oxygen species</p></def></def-item><def-item><term>SNP</term><def><p>single-nucleotide polymorphism</p></def></def-item><def-item><term>TLS</term><def><p>translesion synthesis</p></def></def-item><def-item><term>TSCC</term><def><p>tongue squamous cell carcinoma</p></def></def-item><def-item><term>USP1</term><def><p>ubiquitin specific peptidase 1</p></def></def-item><def-item><term>VDAC1</term><def><p>voltage-dependent anion channel 1</p></def></def-item></def-list></glossary><fn-group><fn><p><xref ref-type="supplementary-material" rid="sup1">Supplementary Information</xref> accompanies this paper on Cell Death and Disease website (http://www.nature.com/cddis)</p></fn><fn><p>Edited by B Zhivotovsky</p></fn></fn-group><notes><p>The authors declare no conflict of interest.</p></notes><ref-list><ref id="bib1"><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Peyrone</surname><given-names>M</given-names></name></person-group><article-title>Ueber die Einwirkung des Ammoniaks auf Platinchlorür</article-title><source>Ann Chemie Pharm</source><year>1844</year><volume>51</volume><fpage>1</fpage><lpage>29</lpage></mixed-citation></ref><ref id="bib2"><mixed-citation publication-type="journal"><person-group 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xlink:href="cddis2013428x1.doc"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material></sec></back><floats-group><fig id="fig1"><label>Figure 1</label><caption><p>Mode of action of cisplatin. As a result of the reduced cytoplasmic concentration of chloride ions, intracellular cisplatin (CDDP) is rapidly ‘aquated', hence acquiring a pronounced electrophilic reactivity. Aquated CDDP binds with high affinity to nuclear DNA, in particular to nucleophilic N7 sites on purines, thereby promoting the activation of the DNA damage response. In addition, CDDP can physically interact with several cytoplasmic nucleophiles, including mitochondrial DNA (mtDNA) as well as multiple mitochondrial and extramitochondrial proteins, hence (i) favoring the establishment of oxidative and reticular stress; (ii) eliciting a signal transduction cascade that involves the pro-apoptotic BCL-2 family members BAK1 and BAX, as well as voltage-dependent anion channel 1 (VDAC1) and (iii) activating the cytoplasmic pool of p53. The relative contribution of these nuclear and cytoplasmic modules to the cytostatic/cytotoxic activity of CDDP remains to be precisely elucidated and may exhibit an elevated degree of context dependency. Asterisks tag the primary consequences of CDDP reactivity. ER, endoplasmic reticulum; MOMP, mitochondrial outer membrane permeabilization</p></caption><graphic xlink:href="cddis2013428f1"></graphic></fig><fig id="fig2"><label>Figure 2</label><caption><p>Molecular mechanisms of cisplatin resistance. Malignant cells can lose their sensitivity to the cytostatic/cytotoxic activity of cisplatin (CDDP) as a result of a wide panel of genetic or epigenetic defects. These alterations can (i) affect processes that precede the actual binding of CDDP to its targets (pre-target resistance); (ii) potentiate the ability of cells to repair the molecular damage caused by CDDP (on-target resistance); (iii) impair the transmission of signals that normally relay such a CDDP-induced damage to cell senescence or apoptosis (post-target resistance) or (iv) stimulate the delivery of pro-survival signals that antagonize CDDP cytotoxicity although they are normally not elicited by this drug (off-target resistance). Of note, CDDP resistance is generally multifactorial, that is, it relies on the activation of several, non-overlapping mechanisms that concur to limit the cytostatic/cytotoxic effects of CDDP at multiple levels. At least in part, this explains why efficient strategies to increase the sensitivity of human neoplasms to CDDP are still lacking in spite of a prolonged and intense wave of investigation. ATP7B, ATPase, Cu<sup>2+</sup> transporting, <italic>β</italic> polypeptide; CTR1, copper transporter 1; MRP2, multidrug resistance-associated protein 2; UPR, unfolded protein response. CDDP aquation is depicted in red</p></caption><graphic xlink:href="cddis2013428f2"></graphic></fig></floats-group></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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