Biological functions of CDK5 and potential CDK5 targeted clinical treatments
Identifieur interne : 000747 ( Main/Exploration ); précédent : 000746; suivant : 000748Biological functions of CDK5 and potential CDK5 targeted clinical treatments
Auteurs : Alison Shupp [États-Unis] ; Mathew C. Casimiro [États-Unis] ; Richard G. Pestell [États-Unis]Source :
- Oncotarget [ 1949-2553 ] ; 2017.
Abstract
Cyclin dependent kinases are proline-directed serine/threonine protein kinases that are traditionally activated upon association with a regulatory subunit. For most CDKs, activation by a cyclin occurs through association and phosphorylation of the CDK’s T-loop. CDK5 is unusual because it is not typically activated upon binding with a cyclin and does not require T-loop phosphorylation for activation, even though it has high amino acid sequence homology with other CDKs. While it was previously thought that CDK5 only interacted with p35 or p39 and their cleaved counterparts, Recent evidence suggests that CDK5 can interact with certain cylins, amongst other proteins, which modulate CDK5 activity levels. This review discusses recent findings of molecular interactions that regulate CDK5 activity and CDK5 associated pathways that are implicated in various diseases. Also covered herein is the growing body of evidence for CDK5 in contributing to the onset and progression of tumorigenesis.
Url:
DOI: 10.18632/oncotarget.14538
PubMed: 28077789
PubMed Central: 5370047
Affiliations:
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Casimiro</name><affiliation wicri:level="1"><nlm:aff id="A2"> Pennsylvania Cancer and Regenerative Medicine Research Center, Baruch S Blumberg Institute, Doylestown, PA, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea> Pennsylvania Cancer and Regenerative Medicine Research Center, Baruch S Blumberg Institute, Doylestown, PA</wicri:regionArea><wicri:noRegion>PA</wicri:noRegion></affiliation></author><author><name sortKey="Pestell, Richard G" sort="Pestell, Richard G" uniqKey="Pestell R" first="Richard G." last="Pestell">Richard G. Pestell</name><affiliation wicri:level="1"><nlm:aff id="A2"> Pennsylvania Cancer and Regenerative Medicine Research Center, Baruch S Blumberg Institute, Doylestown, PA, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea> Pennsylvania Cancer and Regenerative Medicine Research Center, Baruch S Blumberg Institute, Doylestown, PA</wicri:regionArea><wicri:noRegion>PA</wicri:noRegion></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">28077789</idno><idno type="pmc">5370047</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370047</idno><idno type="RBID">PMC:5370047</idno><idno type="doi">10.18632/oncotarget.14538</idno><date when="2017">2017</date><idno type="wicri:Area/Pmc/Corpus">004B46</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">004B46</idno><idno type="wicri:Area/Pmc/Curation">004B45</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Curation">004B45</idno><idno type="wicri:Area/Pmc/Checkpoint">000378</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Checkpoint">000378</idno><idno type="wicri:Area/Ncbi/Merge">008C00</idno><idno type="wicri:Area/Ncbi/Curation">008C00</idno><idno type="wicri:Area/Ncbi/Checkpoint">008C00</idno><idno type="wicri:Area/Main/Merge">000748</idno><idno type="wicri:Area/Main/Curation">000747</idno><idno type="wicri:Area/Main/Exploration">000747</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Biological functions of CDK5 and potential CDK5 targeted clinical treatments</title><author><name sortKey="Shupp, Alison" sort="Shupp, Alison" uniqKey="Shupp A" first="Alison" last="Shupp">Alison Shupp</name><affiliation wicri:level="1"><nlm:aff id="A1"> Departments of Cancer Biology, Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea> Departments of Cancer Biology, Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA</wicri:regionArea><wicri:noRegion>PA</wicri:noRegion></affiliation></author><author><name sortKey="Casimiro, Mathew C" sort="Casimiro, Mathew C" uniqKey="Casimiro M" first="Mathew C." last="Casimiro">Mathew C. Casimiro</name><affiliation wicri:level="1"><nlm:aff id="A2"> Pennsylvania Cancer and Regenerative Medicine Research Center, Baruch S Blumberg Institute, Doylestown, PA, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea> Pennsylvania Cancer and Regenerative Medicine Research Center, Baruch S Blumberg Institute, Doylestown, PA</wicri:regionArea><wicri:noRegion>PA</wicri:noRegion></affiliation></author><author><name sortKey="Pestell, Richard G" sort="Pestell, Richard G" uniqKey="Pestell R" first="Richard G." last="Pestell">Richard G. Pestell</name><affiliation wicri:level="1"><nlm:aff id="A2"> Pennsylvania Cancer and Regenerative Medicine Research Center, Baruch S Blumberg Institute, Doylestown, PA, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea> Pennsylvania Cancer and Regenerative Medicine Research Center, Baruch S Blumberg Institute, Doylestown, PA</wicri:regionArea><wicri:noRegion>PA</wicri:noRegion></affiliation></author></analytic><series><title level="j">Oncotarget</title><idno type="eISSN">1949-2553</idno><imprint><date when="2017">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Cyclin dependent kinases are proline-directed serine/threonine protein kinases that are traditionally activated upon association with a regulatory subunit. For most CDKs, activation by a cyclin occurs through association and phosphorylation of the CDK’s T-loop. CDK5 is unusual because it is not typically activated upon binding with a cyclin and does not require T-loop phosphorylation for activation, even though it has high amino acid sequence homology with other CDKs. While it was previously thought that CDK5 only interacted with p35 or p39 and their cleaved counterparts, Recent evidence suggests that CDK5 can interact with certain cylins, amongst other proteins, which modulate CDK5 activity levels. This review discusses recent findings of molecular interactions that regulate CDK5 activity and CDK5 associated pathways that are implicated in various diseases. Also covered herein is the growing body of evidence for CDK5 in contributing to the onset and progression of tumorigenesis.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Shah, K" uniqKey="Shah K">K Shah</name></author><author><name sortKey="Lahiri, Dk" uniqKey="Lahiri D">DK. 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J">J Hessler</name></author><author><name sortKey="Grever, Mr" uniqKey="Grever M">MR Grever</name></author><author><name sortKey="E, Im" uniqKey="E I">Im E</name></author><author><name sortKey="Zhou, H" uniqKey="Zhou H">H Zhou</name></author><author><name sortKey="Zhu, Y" uniqKey="Zhu Y">Y Zhu</name></author><author><name sortKey="Zhang, D" uniqKey="Zhang D">D Zhang</name></author><author><name sortKey="Small, K" uniqKey="Small K">K Small</name></author><author><name sortKey="Et, Al" uniqKey="Et A">al et</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Sundaram, Jr" uniqKey="Sundaram J">JR Sundaram</name></author><author><name sortKey="Poore, Cp" uniqKey="Poore C">CP Poore</name></author><author><name sortKey="Sulaimee, Nh" uniqKey="Sulaimee N">NH Sulaimee</name></author><author><name sortKey="Pareek, T" uniqKey="Pareek T">T Pareek</name></author><author><name sortKey="Asad, Ab" uniqKey="Asad A">AB Asad</name></author><author><name sortKey="Rajkumar, R" uniqKey="Rajkumar R">R Rajkumar</name></author><author><name sortKey="Cheong, Wf" uniqKey="Cheong W">WF Cheong</name></author><author><name sortKey="Wenk, Mr" uniqKey="Wenk M">MR Wenk</name></author><author><name sortKey="Dawe, Gs" uniqKey="Dawe G">GS Dawe</name></author><author><name sortKey="Chuang, Kh" uniqKey="Chuang K">KH Chuang</name></author><author><name sortKey="Pant, Hc" uniqKey="Pant H">HC Pant</name></author><author><name sortKey="Kesavapany, S" uniqKey="Kesavapany S">S Kesavapany</name></author></analytic></biblStruct></listBibl></div1></back></TEI><affiliations><list><country><li>États-Unis</li></country></list><tree><country name="États-Unis"><noRegion><name sortKey="Shupp, Alison" sort="Shupp, Alison" uniqKey="Shupp A" first="Alison" last="Shupp">Alison Shupp</name></noRegion><name sortKey="Casimiro, Mathew C" sort="Casimiro, Mathew C" uniqKey="Casimiro M" first="Mathew C." last="Casimiro">Mathew C. Casimiro</name><name sortKey="Pestell, Richard G" sort="Pestell, Richard G" uniqKey="Pestell R" first="Richard G." last="Pestell">Richard G. Pestell</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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