TY - JOUR
T1 - Context is everything
T2 - aneuploidy in cancer
AU - Ben-David, Uri
AU - Amon, Angelika
N1 - Publisher Copyright:
© 2019, Springer Nature Limited.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Cancer 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.
AB - Cancer 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.
UR - http://www.scopus.com/inward/record.url?scp=85073958485&partnerID=8YFLogxK
U2 - 10.1038/s41576-019-0171-x
DO - 10.1038/s41576-019-0171-x
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C2 - 31548659
AN - SCOPUS:85073958485
SN - 1471-0056
VL - 21
SP - 44
EP - 62
JO - Nature Reviews Genetics
JF - Nature Reviews Genetics
IS - 1
ER -