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dc.contributor.authorBen-David, Uri
dc.contributor.authorAmon, Angelika B
dc.date.accessioned2020-07-16T20:38:23Z
dc.date.available2020-07-16T20:38:23Z
dc.date.issued2019-09
dc.date.submitted2019-08
dc.identifier.issn1471-0064
dc.identifier.urihttps://hdl.handle.net/1721.1/126231
dc.description.abstractCancer is driven by multiple types of genetic alterations, which range in size from point mutations to whole-chromosome gains and losses, known as aneuploidy. Chromosome instability, the process that gives rise to aneuploidy, can promote tumorigenesis by increasing genetic heterogeneity and promoting tumour evolution. However, much less is known about how aneuploidy itself contributes to tumour formation and progression. Unlike some pan-cancer oncogenes and tumour suppressor genes that drive transformation in virtually all cell types and cellular contexts, aneuploidy is not a universal promoter of tumorigenesis. Instead, recent studies suggest that aneuploidy is a context-dependent, cancer-type-specific oncogenic event that may have clinical relevance as a prognostic marker and as a potential therapeutic target. ©2019, Springer Nature Limited.en_US
dc.description.sponsorshipNIH grant CA206157en_US
dc.description.sponsorshipNIH grant GM118066en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionofhttps://dx.doi.org/10.1038/S41576-019-0171-Xen_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceProf. Amon via Courtney Crummetten_US
dc.titleContext is everything: aneuploidy in canceren_US
dc.typeArticleen_US
dc.identifier.citationBen-David, Uri and Angelika Amon, "Context is everything: aneuploidy in cancer." Nature Reviews Genetics 21, 1 (January 2020): p. 44–62 doi. 10.1038/s41576-019-0171-x ©2019 Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.relation.journalNature Reviews Geneticsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-07-16T16:51:49Z
dspace.date.submission2020-07-16T16:51:52Z
mit.journal.volume21en_US
mit.journal.issue1en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusComplete


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