| Literature DB >> 29622463 |
Alison M Taylor1, Juliann Shih2, Gavin Ha1, Galen F Gao2, Xiaoyang Zhang1, Ashton C Berger2, Steven E Schumacher3, Chen Wang4, Hai Hu5, Jianfang Liu5, Alexander J Lazar6, Andrew D Cherniack1, Rameen Beroukhim1, Matthew Meyerson7.
Abstract
Aneuploidy, whole chromosome or chromosome arm imbalance, is a near-universal characteristic of human cancers. In 10,522 cancer genomes from The Cancer Genome Atlas, aneuploidy was correlated with TP53 mutation, somatic mutation rate, and expression of proliferation genes. Aneuploidy was anti-correlated with expression of immune signaling genes, due to decreased leukocyte infiltrates in high-aneuploidy samples. Chromosome arm-level alterations show cancer-specific patterns, including loss of chromosome arm 3p in squamous cancers. We applied genome engineering to delete 3p in lung cells, causing decreased proliferation rescued in part by chromosome 3 duplication. This study defines genomic and phenotypic correlates of cancer aneuploidy and provides an experimental approach to study chromosome arm aneuploidy.Entities:
Keywords: aneuploidy; cancer genomics; genome engineering; lung squamous cell carcinoma
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Year: 2018 PMID: 29622463 PMCID: PMC6028190 DOI: 10.1016/j.ccell.2018.03.007
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743