Title: Rare Variants in the DNA Repair Pathway and the Risk of Colorectal Cancer.

Authors: Matejcic, Marco; Shaban, Hiba A; Quintana, Melanie W; Schumacher, Fredrick R; Edlund, Christopher K; Naghi, Leah; Pai, Rish K; Haile, Robert W; Levine, A Joan; Buchanan, Daniel D; Jenkins, Mark A; Figueiredo, Jane C; Rennert, Gad; Gruber, Stephen B; Li, Li; Casey, Graham; Conti, David V; Schmit, Stephanie L

Published In Cancer Epidemiol Biomarkers Prev, (2021 05)

Abstract: BACKGROUND: Inherited susceptibility is an important contributor to colorectal cancer risk, and rare variants in key genes or pathways could account in part for the missing proportion of colorectal cancer heritability. METHODS: We conducted an exome-wide association study including 2,327 cases and 2,966 controls of European ancestry from three large epidemiologic studies. Single variant associations were tested using logistic regression models, adjusting for appropriate study-specific covariates. In addition, we examined the aggregate effects of rare coding variation at the gene and pathway levels using Bayesian model uncertainty techniques. RESULTS: In an exome-wide gene-level analysis, we identified ST6GALNAC2 as the top associated gene based on the Bayesian risk index (BRI) method [summary Bayes factor (BF)BRI = 2604.23]. A rare coding variant in this gene, rs139401613, was the top associated variant (P = 1.01 × 10-6) in an exome-wide single variant analysis. Pathway-level association analyses based on the integrative BRI (iBRI) method found extreme evidence of association with the DNA repair pathway (BFiBRI = 17852.4), specifically with the nonhomologous end joining (BFiBRI = 437.95) and nucleotide excision repair (BFiBRI = 36.96) subpathways. The iBRI method also identified RPA2, PRKDC, ERCC5, and ERCC8 as the top associated DNA repair genes (summary BFiBRI ≥ 10), with rs28988897, rs8178232, rs141369732, and rs201642761 being the most likely associated variants in these genes, respectively. CONCLUSIONS: We identified novel variants and genes associated with colorectal cancer risk and provided additional evidence for a role of DNA repair in colorectal cancer tumorigenesis. IMPACT: This study provides new insights into the genetic predisposition to colorectal cancer, which has potential for translation into improved risk prediction.

PubMed ID: 33627384

MeSH Terms: Bayes Theorem; Colorectal Neoplasms/genetics*; DNA Repair/genetics*; Genetic Predisposition to Disease*; Genome-Wide Association Study; Humans; Polymorphism, Single Nucleotide; Risk Factors; Sialyltransferases; Whites