Please use this identifier to cite or link to this item: 10.1002/gepi.22288
Title: Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
Authors: Feng, Helian
Gusev, Alexander
Pasaniuc, Bogdan
GEMO Study Collaborators
Nikitina-Zake, Liene
Keywords: Breast Neoplasms/genetics;Estrogens/metabolism;Female;Genetic Predisposition to Disease;Genome-Wide Association Study;Genomics;Humans;Receptors, Estrogen/metabolism;Risk Assessment;Transcriptome;Vesicular Transport Proteins/genetics;1.6 Biological sciences;3.1 Basic medicine;1.1. Scientific article indexed in Web of Science and/or Scopus database;SDG 3 - Good Health and Well-being
Issue Date: Jul-2020
Citation: Feng , H , Gusev , A , Pasaniuc , B , GEMO Study Collaborators & Nikitina-Zake , L 2020 , ' Transcriptome-wide association study of breast cancer risk by estrogen-receptor status ' , Genetic Epidemiology , vol. 44 , no. 5 , pp. 442-468 . https://doi.org/10.1002/gepi.22288
Abstract: Previous transcriptome-wide association studies (TWAS) have identified breast cancer risk genes by integrating data from expression quantitative loci and genome-wide association studies (GWAS), but analyses of breast cancer subtype-specific associations have been limited. In this study, we conducted a TWAS using gene expression data from GTEx and summary statistics from the hitherto largest GWAS meta-analysis conducted for breast cancer overall, and by estrogen receptor subtypes (ER+ and ER-). We further compared associations with ER+ and ER- subtypes, using a case-only TWAS approach. We also conducted multigene conditional analyses in regions with multiple TWAS associations. Two genes, STXBP4 and HIST2H2BA, were specifically associated with ER+ but not with ER- breast cancer. We further identified 30 TWAS-significant genes associated with overall breast cancer risk, including four that were not identified in previous studies. Conditional analyses identified single independent breast-cancer gene in three of six regions harboring multiple TWAS-significant genes. Our study provides new information on breast cancer genetics and biology, particularly about genomic differences between ER+ and ER- breast cancer.
Description: © 2020 The Authors. Genetic Epidemiology published by Wiley Periodicals, Inc.
DOI: 10.1002/gepi.22288
ISSN: 0741-0395
Appears in Collections:Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure



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