DESCRIPTION (provided by applicant): We propose to study the relations between
common potentially low-penetrance polymorphisms in candidate genes for breast
cancer in three prospective cohorts; the Nurses' Health Studies I and II, and
the Women's Health Study. Specific hypotheses relate variants in genes
important to steroid hormone metabolism (sex-hormone binding globulin, CYP 19
and the progesterone receptor) with risk of breast cancer, and effect
modification of the relation of postmenopausal hormone use with breast cancer
by genotype. We will also examine polymorphisms in two genes involved in cell
cycle control (the HER2 proto-oncogene, the TGFbeta receptor type I) that have
been associated with breast cancer risk in other studies. Finally, we will seek
to replicate interactions we observed in the current grant cycle between
initiation of smoking at a young age and variants in the CYP1A1 gene, and first
degree family history of breast cancer and longer (CAG)n repeats in the
androgen receptor. We estimate we will accrue 1540 cases of breast cancer in
the Nurses' Health Study I, 261 cases in the Nurses' Health Study II, and 1050
cases in the Women's Health Study. With this total of 2851 incident cases, we
will have >90 percent power to detect relative risks of 1.5 or greater for the
main effects of most of the genotypes of interest. We will also have
substantial power to detect interactions between these genotypes and
established breast cancer risk factors.
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