Serveur d'exploration Chloroquine

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Targeting the lysosome in cancer

Identifieur interne : 000D87 ( Main/Exploration ); précédent : 000D86; suivant : 000D88

Targeting the lysosome in cancer

Auteurs : Shengfu Piao [États-Unis] ; Ravi K. Amaravadi [États-Unis]

Source :

RBID : ISTEX:52244FD8572E0927E7BCFCDFF5F15A80C164EE1C

Abstract

Lysosomes are membrane‐bound intracellular organelles that receive macromolecules delivered by endocytosis, phagocytosis, and autophagy for degradation and recycling. Over the last decade, advances in lysosome research have established a broad role for the lysosome in the pathophysiology of disease. In this review, we highlight the recent discoveries in lysosome biology, with an emphasis on their implications for cancer therapy. We focus on targeting the lysosome in cancer by exploring lysosomal biogenesis and its role in the crosstalk between apoptosis and autophagy. We also discuss how lysosomal inhibition could emerge as a new therapeutic strategy to overcome drug resistance in cancer.

Url:
DOI: 10.1111/nyas.12953


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Targeting the lysosome in cancer</title>
<author>
<name sortKey="Piao, Shengfu" sort="Piao, Shengfu" uniqKey="Piao S" first="Shengfu" last="Piao">Shengfu Piao</name>
</author>
<author>
<name sortKey="Amaravadi, Ravi K" sort="Amaravadi, Ravi K" uniqKey="Amaravadi R" first="Ravi K." last="Amaravadi">Ravi K. Amaravadi</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:52244FD8572E0927E7BCFCDFF5F15A80C164EE1C</idno>
<date when="2016" year="2016">2016</date>
<idno type="doi">10.1111/nyas.12953</idno>
<idno type="url">https://api.istex.fr/ark:/67375/WNG-K2PV672D-N/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000C72</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000C72</idno>
<idno type="wicri:Area/Istex/Curation">000C72</idno>
<idno type="wicri:Area/Istex/Checkpoint">000006</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">000006</idno>
<idno type="wicri:doubleKey">0077-8923:2016:Piao S:targeting:the:lysosome</idno>
<idno type="wicri:Area/Main/Merge">000D88</idno>
<idno type="wicri:Area/Main/Curation">000D87</idno>
<idno type="wicri:Area/Main/Exploration">000D87</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main">Targeting the lysosome in cancer</title>
<author>
<name sortKey="Piao, Shengfu" sort="Piao, Shengfu" uniqKey="Piao S" first="Shengfu" last="Piao">Shengfu Piao</name>
<affiliation wicri:level="3">
<country>États-Unis</country>
<placeName>
<settlement type="city">Philadelphie</settlement>
<region type="state">Pennsylvanie</region>
</placeName>
<wicri:orgArea>Department of Medicine and Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Pennsylvania</wicri:orgArea>
</affiliation>
</author>
<author>
<name sortKey="Amaravadi, Ravi K" sort="Amaravadi, Ravi K" uniqKey="Amaravadi R" first="Ravi K." last="Amaravadi">Ravi K. Amaravadi</name>
<affiliation wicri:level="3">
<country>États-Unis</country>
<placeName>
<settlement type="city">Philadelphie</settlement>
<region type="state">Pennsylvanie</region>
</placeName>
<wicri:orgArea>Department of Medicine and Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Pennsylvania</wicri:orgArea>
</affiliation>
<affiliation wicri:level="1">
<country wicri:rule="url">États-Unis</country>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j" type="main">Annals of the New York Academy of Sciences</title>
<title level="j" type="sub">Targeting the Lysosome</title>
<title level="j" type="alt">ANNALS OF THE NEW YORK ACADEMY OF SCIENCES</title>
<idno type="ISSN">0077-8923</idno>
<idno type="eISSN">1749-6632</idno>
<imprint>
<biblScope unit="vol">1371</biblScope>
<biblScope unit="issue">1</biblScope>
<biblScope unit="page" from="45">45</biblScope>
<biblScope unit="page" to="54">54</biblScope>
<biblScope unit="page-count">10</biblScope>
<date type="published" when="2016-05">2016-05</date>
</imprint>
<idno type="ISSN">0077-8923</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0077-8923</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract">Lysosomes are membrane‐bound intracellular organelles that receive macromolecules delivered by endocytosis, phagocytosis, and autophagy for degradation and recycling. Over the last decade, advances in lysosome research have established a broad role for the lysosome in the pathophysiology of disease. In this review, we highlight the recent discoveries in lysosome biology, with an emphasis on their implications for cancer therapy. We focus on targeting the lysosome in cancer by exploring lysosomal biogenesis and its role in the crosstalk between apoptosis and autophagy. We also discuss how lysosomal inhibition could emerge as a new therapeutic strategy to overcome drug resistance in cancer.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>Pennsylvanie</li>
</region>
<settlement>
<li>Philadelphie</li>
</settlement>
</list>
<tree>
<country name="États-Unis">
<region name="Pennsylvanie">
<name sortKey="Piao, Shengfu" sort="Piao, Shengfu" uniqKey="Piao S" first="Shengfu" last="Piao">Shengfu Piao</name>
</region>
<name sortKey="Amaravadi, Ravi K" sort="Amaravadi, Ravi K" uniqKey="Amaravadi R" first="Ravi K." last="Amaravadi">Ravi K. Amaravadi</name>
<name sortKey="Amaravadi, Ravi K" sort="Amaravadi, Ravi K" uniqKey="Amaravadi R" first="Ravi K." last="Amaravadi">Ravi K. Amaravadi</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000D87 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000D87 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    ChloroquineV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:52244FD8572E0927E7BCFCDFF5F15A80C164EE1C
   |texte=   Targeting the lysosome in cancer
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Wed Mar 25 22:43:59 2020. Site generation: Sun Jan 31 12:44:45 2021