A joint transcriptome-wide association study across multiple tissues identifies candidate breast cancer susceptibility genes.

Am J Hum Genet

Department of Public Health Sciences, University of Chicago, Chicago, IL 60637, USA; Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, IL 60637, USA. Electronic address:

Published: June 2023

AI Article Synopsis

  • Genome-wide association studies (GWASs) have pinpointed over 200 genomic loci linked to breast cancer risk, but many causal genes remain unidentified.
  • A joint analysis combining results from the UK Biobank and the Breast Cancer Association Consortium revealed eight new loci and identified 309 significant genes associated with breast cancer through transcriptome-wide association studies (TWASs).
  • The study enhances understanding of breast cancer genetics by mapping candidate genes in existing loci while also uncovering new genomic regions related to the disease.

Article Abstract

Genome-wide association studies (GWASs) have identified more than 200 genomic loci for breast cancer risk, but specific causal genes in most of these loci have not been identified. In fact, transcriptome-wide association studies (TWASs) of breast cancer performed using gene expression prediction models trained in breast tissue have yet to clearly identify most target genes. To identify candidate genes, we performed a GWAS analysis in a breast cancer dataset from UK Biobank (UKB) and combined the results with the GWAS results of the Breast Cancer Association Consortium (BCAC) by a meta-analysis. Using the summary statistics from the meta-analysis, we performed a joint TWAS analysis that combined TWAS signals from multiple tissues. We used expression prediction models trained in 11 tissues that are potentially relevant to breast cancer from the Genotype-Tissue Expression (GTEx) data. In the GWAS analysis, we identified eight loci distinct from those reported previously. In the TWAS analysis, we identified 309 genes at 108 genomic loci to be significantly associated with breast cancer at the Bonferroni threshold. Of these, 17 genes were located in eight regions that were at least 1 Mb away from published GWAS hits. The remaining TWAS-significant genes were located in 100 known genomic loci from previous GWASs of breast cancer. We found that 21 genes located in known GWAS loci remained statistically significant after conditioning on previous GWAS index variants. Our study provides insights into breast cancer genetics through mapping candidate target genes in a large proportion of known GWAS loci and discovering multiple new loci.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257003PMC
http://dx.doi.org/10.1016/j.ajhg.2023.04.005DOI Listing

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