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dc.contributor.authorReplogle, John Michael
dc.contributor.authorZhou, Wen
dc.contributor.authorAmaro, Adrianna E
dc.contributor.authorMcFarland, James M
dc.contributor.authorVillalobos-Ortiz, Mariana
dc.contributor.authorRyan, Jeremy
dc.contributor.authorLetai, Anthony
dc.contributor.authorYilmaz, Omer
dc.contributor.authorSheltzer, Jason
dc.contributor.authorLippard, Stephen J
dc.contributor.authorBen-David, Uri
dc.contributor.authorAmon, Angelika
dc.date.accessioned2021-10-27T19:52:11Z
dc.date.available2021-10-27T19:52:11Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/133334
dc.description.abstract© 2020 National Academy of Sciences. All rights reserved. Aneuploidy, defined as whole chromosome gains and losses, is associated with poor patient prognosis in many cancer types. However, the condition causes cellular stress and cell cycle delays, foremost in G1 and S phase. Here, we investigate how aneuploidy causes both slow proliferation and poor disease outcome. We test the hypothesis that aneuploidy brings about resistance to chemotherapies because of a general feature of the aneuploid condition—G1 delays. We show that single chromosome gains lead to increased resistance to the frontline chemotherapeutics cisplatin and paclitaxel. Furthermore, G1 cell cycle delays are sufficient to increase chemotherapeutic resistance in euploid cells. Mechanistically, G1 delays increase drug resistance to cisplatin and paclitaxel by reducing their ability to damage DNA and microtubules, respectively. Finally, we show that our findings are clinically relevant. Aneuploidy correlates with slowed proliferation and drug resistance in the Cancer Cell Line Encyclopedia (CCLE) dataset. We conclude that a general and seemingly detrimental effect of aneuploidy, slowed proliferation, provides a selective benefit to cancer cells during chemotherapy treatment.
dc.language.isoen
dc.publisherProceedings of the National Academy of Sciences
dc.relation.isversionof10.1073/pnas.2009506117
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
dc.sourcePNAS
dc.titleAneuploidy increases resistance to chemotherapeutics by antagonizing cell division
dc.typeArticle
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistry
dc.contributor.departmentHoward Hughes Medical Institute
dc.relation.journalProceedings of the National Academy of Sciences of the United States of America
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-08-05T14:50:06Z
dspace.orderedauthorsReplogle, JM; Zhou, W; Amaro, AE; McFarland, JM; Villalobos-Ortiz, M; Ryan, J; Letai, A; Yilmaz, O; Sheltzer, J; Lippard, SJ; Ben-David, U; Amon, A
dspace.date.submission2021-08-05T14:50:08Z
mit.journal.volume117
mit.journal.issue48
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


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