| Literature DB >> 18708391 |
Parveen Bhatti1, Michele M Doody, Bruce H Alexander, Jeff Yuenger, Steven L Simon, Robert M Weinstock, Marvin Rosenstein, Marilyn Stovall, Michael Abend, Dale L Preston, Paul Pharoah, Jeffery P Struewing, Alice J Sigurdson.
Abstract
Genome-wide association studies are discovering relationships between single-nucleotide polymorphisms and breast cancer, but the functions of these single-nucleotide polymorphisms are unknown and environmental exposures are likely to be important. We assessed whether breast cancer risk single-nucleotide polymorphisms interacted with ionizing radiation, a known breast carcinogen, among 859 cases and 1,083 controls nested in the U.S. Radiologic Technologists cohort. Among 11 Breast Cancer Association Consortium risk single-nucleotide polymorphisms, we found that the genotype-associated breast cancer risk varied significantly by radiation dose for rs2107425 in the H19 gene (P(interaction) = 0.001). H19 is a maternally expressed imprinted mRNA that is closely involved in regulating the IGF2 gene and could exert its influence by this or by some other radiation-related pathway.Entities:
Mesh:
Year: 2008 PMID: 18708391 PMCID: PMC2583248 DOI: 10.1158/1055-9965.EPI-08-0300
Source DB: PubMed Journal: Cancer Epidemiol Biomarkers Prev ISSN: 1055-9965 Impact factor: 4.254