| Literature DB >> 33203674 |
John Michael Replogle1, Wen Zhou2,3, Adrianna E Amaro2, James M McFarland4, Mariana Villalobos-Ortiz5, Jeremy Ryan5, Anthony Letai5,6, Omer Yilmaz2, Jason Sheltzer7, Stephen J Lippard2,3, Uri Ben-David8, Angelika Amon2,9.
Abstract
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.Entities:
Keywords: aneuploidy; cell cycle; chemotherapy resistance; cisplatin; paclitaxel
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Year: 2020 PMID: 33203674 PMCID: PMC7720170 DOI: 10.1073/pnas.2009506117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205