The CYP1A2 Genotype Modifies the Association Between Coffee Consumption and Breast Cancer Risk Among BRCA1 Mutation Carriers

基因型 乳腺癌 突变 遗传学 肿瘤科 医学 内科学 生物 癌症 基因
作者
Joanne Kotsopoulos,Parviz Ghadirian,Ahmed El‐Sohemy,Henry T. Lynch,Carrie Snyder,Mary B. Daly,Susan M. Domchek,Susan Randall,Beth Y. Karlan,Phil Zhang,Shiyu Zhang,Ping Sun,Steven A. Narod
出处
期刊:Cancer Epidemiology, Biomarkers & Prevention [American Association for Cancer Research]
卷期号:16 (5): 912-916 被引量:76
标识
DOI:10.1158/1055-9965.epi-06-1074
摘要

Abstract We have recently reported that, among BRCA1 mutation carriers, the consumption of caffeinated coffee was associated with a significant reduction in breast cancer risk. Because the metabolism of caffeine is primarily by CYP1A2, we examined whether or not the CYP1A2 genotype modifies the association between a history of coffee consumption and the risk of breast cancer. A common A to C polymorphism in the CYP1A2 gene is associated with decreased enzyme inducibility and impaired caffeine metabolism. Information regarding coffee consumption habits and the CYP1A2 genotype was available for 411 BRCA1 mutation carriers (170 cases and 241 controls). We estimated the odds ratios (ORs) and 95% confidence intervals (95% CIs) for breast cancer associated with the CYP1A2 genotype and a history of coffee consumption before age 35, adjusting for potential confounders. The CYP1A2 genotype did not affect breast cancer risk. Among women with at least one variant C allele (AC or CC), those who consumed coffee had a 64% reduction in breast cancer risk, compared with women who never consumed coffee (OR, 0.36; 95% CI, 0.18-0.73). A significant protective effect of coffee consumption was not observed among women with the CYP1A2 AA genotype (OR, 0.93; 95% CI, 0.49-1.77). Similar results were obtained when the analysis was restricted to caffeinated coffee. This study suggests that caffeine protects against breast cancer in women with a BRCA1 mutation and illustrates the importance of integrating individual genetic variability when assessing diet-disease associations. (Cancer Epidemiol Biomarkers Prev 2007;16(5):912–6)
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