Статья

TRANSCRIPTOME-WIDE ASSOCIATION STUDY OF BREAST CANCER RISK BY ESTROGEN-RECEPTOR STATUS

FENG, H., KRAFT, P., JIANG, X., GUSEV, A., PASANIUC, B., WU, L., LONG, J., CAI, Q., SHU, X.O., ZHENG, W., ABU-FULL, Z., RENNERT, G., AITTOMÄKI, K., ANDRULIS, I.L., GLENDON, G., ANTON-CULVER, H., ZIOGAS, A., ARASON, A., BARKARDOTTIR, R.B., ARNDT, V., BRENNER, H., ARONSON, K.J., ARUN, B.K., ASSERYANIS, E., SINGER, C.F., AUER, P.L., AZZOLLINI, J., MANOUKIAN, S., BALMAÑA, J., BECKMANN, M.W., FASCHING, P.A., BEHRENS, S., CHANG-CLAUDE, J., JUNG, A., KAPOOR, P.M., BENITEZ, J., BLANCO, A., OSORIO, A., VEGA, A., GONZÁLEZ-NEIRA, A., BERMISHEVA, M., KHUSNUTDINOVA, E., BIAŁKOWSKA, K., CYBULSKI, C.
2020

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.

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