Genome-wide association study identifies possible genetic risk factors for colorectal adenomas.

Edwards TL, Shrubsole MJ, Cai Q, Li G, Dai Q, Rex DK, Ulbright TM, Fu Z, Delahanty RH, Murff HJ, Smalley W, Ness RM, Zheng W
Cancer Epidemiol Biomarkers Prev. 2013 22 (7): 1219-26

PMID: 23677573 · PMCID: PMC3716448 · DOI:10.1158/1055-9965.EPI-12-1437

BACKGROUND - Colorectal cancer is the second leading cause of cancer-related death, and most colorectal cancer usually arises from colorectal adenomas. Removal of polyps reduces mortality from colorectal cancer. Colorectal adenomas are known to aggregate in families; however, the genetic determinants for risk of polyps are largely unknown.

METHODS - In this study, we used data from the Tennessee Colorectal Polyp Study and the Tennessee-Indiana Adenoma Recurrence Study to conduct a GWAS of adenoma cases and controls. Our design consisted of discovery and replication phases for a total of 2,551 Caucasian adenoma cases and 3,285 Caucasian controls. We carried out logistic regression to test for association in both the discovery and replication phase and further examined the results with meta-analysis.

RESULTS - No single nucleotide polymorphism (SNP) achieved a genome-wide significant P value; however, the most significantly associated SNPs were either previously associated with colorectal cancer in GWAS, such as rs10505477 in the gene POU5F1 [odds ratio (OR) = 0.87; 95% confidence interval (CI) 0.81-0.94; P = 4.4 × 10(-4)), or have been biologically linked to benign growths in other tissues, such as rs1919314 in the gene histone deacetylase 9 (OR = 1.32; 95% CI, 1.18-1.47; P = 1.1 × 10(-6)).

CONCLUSIONS - This study suggests that several SNPs may be related to adenoma risk and provides clues for future studies.

IMPACT - These results suggest that some known genetic risk factors of colorectal cancer are necessary but not sufficient for carcinogenesis.

MeSH Terms (14)

Adenoma Aged Colorectal Neoplasms DNA Copy Number Variations Female Genetic Predisposition to Disease Genome-Wide Association Study Genotype Humans Male Middle Aged Polymorphism, Single Nucleotide Risk Factors Tennessee

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