No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: A multi-center cohort study
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
Background The transforming growth factor β-1 gene (TGFB1) is a plausible candidate for breast cancer susceptibility. The L10P variant of TGFB1 is associated with higher circulating levels and secretion of TGF-β, and recent large-scale studies suggest strongly that this variant is associated with breast cancer risk in the general population. Methods To evaluate whether TGFB1 L10P also modifies the risk of breast cancer in BRCA1 or BRCA2 mutation carriers, we undertook a multi-center study of 3,442 BRCA1 and 2,095 BRCA2 mutation carriers. Results We found no evidence of association between TGFB1 L10P and breast cancer risk in either BRCA1 or BRCA2 mutation carriers. The per-allele HR for the L10P variant was 1.01 (95%CI: 0.92-1.11) in BRCA1 carriers and 0.92 (95%CI: 0.81-1.04) in BRCA2 mutation carriers. Conclusions These results do not support the hypothesis that TGFB1 L10P genotypes modify the risk of breast cancer in BRCA1 or BRCA2 mutation carriers.
Details
Original language | English |
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Pages (from-to) | 185-192 |
Number of pages | 8 |
Journal | Breast cancer research and treatment |
Volume | 115 |
Issue number | 1 |
Publication status | Published - 1 May 2009 |
Peer-reviewed | Yes |
External IDs
PubMed | 18523885 |
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Keywords
Sustainable Development Goals
ASJC Scopus subject areas
Keywords
- BRCA1, BRCA2, Hereditary cancer, Risk modifiers