Endesfelder, D. ; Burrell, R.A.* ; Kanu, N.* ; McGranahan, N.* ; Howell, M.* ; Parker, P.J.* ; Downward, J.* ; Swanton, C.* ; Kschischo, M.*
Chromosomal instability selects gene copy number variants encoding core regulators of proliferation in ER+ breast cancer.
Cancer Res. 74, 4853-4863 (2014)
Abstract Chromosomal instability (CIN) is associated with poor outcome in epithelial malignancies, including breast carcinomas. Evidence suggests that prognostic signatures in estrogen receptor-positive (ER(+)) breast cancer define tumors with CIN and high proliferative potential. Intriguingly, CIN induction in lower eukaryotic cells and human cells is context dependent, typically resulting in a proliferation disadvantage but conferring a fitness benefit under strong selection pressures. We hypothesized that CIN permits accelerated genomic evolution through the generation of diverse DNA copy-number events that may be selected during disease development. In support of this hypothesis, we found evidence for selection of gene amplification of core regulators of proliferation in CIN-associated cancer genomes. Stable DNA copy-number amplifications of the core regulators TPX2 and UBE2C were associated with expression of a gene module involved in proliferation. The module genes were enriched within prognostic signature gene sets for ER(+) breast cancer, providing a logical connection between CIN and prognostic signature expression. Our results provide a framework to decipher the impact of intratumor heterogeneity on key cancer phenotypes, and they suggest that CIN provides a permissive landscape for selection of copy-number alterations that drive cancer proliferation.
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Publication type
Article: Journal article
Document type
Scientific Article
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Keywords
Expression Profiles; Colorectal-cancer; Aneuploidy; Prognosis; Survival; Cells; Metaanalysis; Subtypes; Biology; Genome
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Language
english
Publication Year
2014
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2014
ISSN (print) / ISBN
0008-5472
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1538-7445
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Volume: 74,
Issue: 17,
Pages: 4853-4863
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American Association for Cancer Research (AACR)
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Philadelphia, Pa.
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Peer reviewed
POF-Topic(s)
30505 - New Technologies for Biomedical Discoveries
Research field(s)
Enabling and Novel Technologies
PSP Element(s)
G-503890-001
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Erfassungsdatum
2014-09-12