DNA repair gene variants in relation to overall cancer risk: a population-based study.
Ontology highlight
ABSTRACT: The hypothesis that germ-line polymorphisms in DNA repair genes influence cancer risk has previously been tested primarily on a cancer site-specific basis. The purpose of this study was to test the hypothesis that DNA repair gene allelic variants contribute to globally elevated cancer risk by measuring associations with risk of all cancers that occurred within a population-based cohort. In the CLUE II cohort study established in 1989 in Washington County, MD, this study was comprised of all 3619 cancer cases ascertained through 2007 compared with a sample of 2296 with no cancer. Associations were measured between 759 DNA repair gene single nucleotide polymorphisms (SNPs) and risk of all cancers. A SNP in O(6)-methylguanine-DNA methyltransferase, MGMT, (rs2296675) was significantly associat
SUBMITTER: Alberg AJ
PROVIDER: S-EPMC3534189 | biostudies-literature | 2013 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA