Abstract | INTRODUCTION: The c.1-34T>C 5' promoter region polymorphism in cytochrome P450c17 ( CYP17), a key enzyme in the biosynthesis of estrogen, has been associated with breast cancer risk, but most previous studies have been relatively small. METHODS: We genotyped 1,544 incident cases of primary breast cancer and 1,502 population controls, all postmenopausal Swedish women, for the CYP17 c.1-34T>C polymorphism and calculated odds ratios ( ORs) and 95% confidence intervals (CIs) from logistic regression models. RESULTS: No overall association was found between CYP17 c.1-34T>C and breast cancer risk, OR 1.0 (95% CI 0.8-1.3) for the A2/A2 (CC) carriers compared to the A1/A1 (TT) carriers, regardless of histopathology. We detected an interaction between CYP17 c.1-34T>C and age at menarche (P = 0.026) but regarded that as a chance finding as no dose-response pattern was evident. Other breast cancer risk factors, including menopausal hormone use and diabetes mellitus, did not modify the overall results. CONCLUSION: It is unlikely that CYP17 c.1-34T>C has a role in breast cancer etiology, overall or in combination with established non-genetic breast cancer risk factors.
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Authors | Kristjana Einarsdóttir, Tove Rylander-Rudqvist, Keith Humphreys, Susanne Ahlberg, Gudrun Jonasdottir, Elisabete Weiderpass, Kee Seng Chia, Magnus Ingelman-Sundberg, Ingemar Persson, Jianjun Liu, Per Hall, Sara Wedrén |
Journal | Breast cancer research : BCR
(Breast Cancer Res)
Vol. 7
Issue 6
Pg. R890-6
( 2005)
ISSN: 1465-542X [Electronic] England |
PMID | 16280037
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Steroid 17-alpha-Hydroxylase
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Topics |
- Aged
- Breast Neoplasms
(genetics)
- Case-Control Studies
- Female
- Genetic Predisposition to Disease
- Humans
- Middle Aged
- Odds Ratio
- Polymorphism, Genetic
- Postmenopause
- Steroid 17-alpha-Hydroxylase
(genetics)
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