4.8 Article

Integrative eQTL-Based Analyses Reveal the Biology of Breast Cancer Risk Loci

Journal

CELL
Volume 152, Issue 3, Pages 633-641

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2012.12.034

Keywords

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Funding

  1. Howard Hughes Medical Institute Physician-Scientist Early Career Awardee
  2. Claudia Adams Barr award
  3. U.S. National Institutes of Health (NIH) [ELLIPSE/GAME-ON-U19 CA148537, R01 CA131341]
  4. Mayer Foundation
  5. H.L. Snyder Medical Foundation
  6. Kohlberg Foundation
  7. A. David Mazzone Awards Program

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Germline determinants of gene expression in tumors are infrequently studied due to the complexity of transcript regulation caused by somatically acquired alterations. We performed expression quantitative trait locus (eQTL)-based analyses using the multi-level information provided in The Cancer Genome Atlas (TCGA). Of the factors we measured, cis-acting eQTLs accounted for 1.2% of the total variation of tumor gene expression, while somatic copy-number alteration and CpG methylation accounted for 7.3% and 3.3%, respectively. eQTL analyses of 15 previously reported breast cancer risk loci resulted in the discovery of three variants that are significantly associated with transcript levels (false discovery rate [FDR] < 0.1). Our trans-based analysis identified an additional three risk loci to act through ESR1, MYC, and KLF4. These findings provide a more comprehensive picture of gene expression determinants in breast cancer as well as insights into the underlying biology of breast cancer risk loci.

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