Li Yu, Millikan Robert C, Bell Douglas A, Cui Lisa, Tse Chiu-Kit J, Newman Beth, Conway Kathleen
Department of Epidemiology, School of Public Heath and Lineberger Comprehensive Cancer Center, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
Breast Cancer Res. 2004;6(4):R460-73. doi: 10.1186/bcr814. Epub 2004 Jun 15.
Previous epidemiologic studies suggest that women with variant cytochrome P4501A1 (CYP1A1) genotypes who smoke cigarettes are at increased risk for breast cancer.
We evaluated the association of breast cancer with CYP1A1 polymorphisms and cigarette smoking in a population-based, case-control study of invasive breast cancer in North Carolina. The study population consisted of 688 cases (271 African Americans and 417 whites) and 702 controls (285 African Americans and 417 whites). Four polymorphisms in CYP1A1 were genotyped using PCR/restriction fragment length polymorphism analysis: M1 (also known as CYP1A12A), M2 (CYP1A12C), M3 (CYP1A13), and M4 (CYP1A14)
No associations were observed for CYP1A1 variant alleles and breast cancer, ignoring smoking. Among women who smoked for longer than 20 years, a modest positive association was found among women with one or more M1 alleles (odds ratio [OR] = 2.1, 95% confidence interval [CI] = 1.2-3.5) but not among women with non-M1 alleles (OR = 1.2, 95% CI = 0.9-1.6). Odds ratios for smoking longer than 20 years were higher among African-American women with one or more M3 alleles (OR = 2.5, 95% CI = 0.9-7.1) compared with women with non-M3 alleles (OR = 1.3, 95% CI = 0.8-2.2). ORs for smoking in white women did not differ appreciably based upon M2 or M4 genotypes.
Cigarette smoking increases breast cancer risk in women with CYP1A1 M1 variant genotypes and in African-American women with CYP1A1 M3 variant genotypes, but the modifying effects of the CYP1A1 genotype are quite weak.
先前的流行病学研究表明,携带细胞色素P4501A1(CYP1A1)基因变异型的吸烟女性患乳腺癌的风险增加。
在北卡罗来纳州一项基于人群的浸润性乳腺癌病例对照研究中,我们评估了乳腺癌与CYP1A1基因多态性及吸烟之间的关联。研究人群包括688例病例(271名非裔美国人和417名白人)和702名对照(285名非裔美国人和417名白人)。使用聚合酶链反应/限制性片段长度多态性分析对CYP1A1中的四种多态性进行基因分型:M1(也称为CYP1A12A)、M2(CYP1A12C)、M3(CYP1A13)和M4(CYP1A14)。
不考虑吸烟因素时,未观察到CYP1A1变异等位基因与乳腺癌之间存在关联。在吸烟超过20年的女性中,发现携带一个或多个M1等位基因的女性存在适度的正相关(比值比[OR]=2.1,95%置信区间[CI]=1.2 - 3.5),而携带非M1等位基因的女性则无此关联(OR = 1.2,95% CI = 0.9 - 1.6)。与携带非M3等位基因的女性(OR = 1.3,95% CI = 0.8 - 2.2)相比,携带一个或多个M3等位基因的非裔美国女性吸烟超过20年的比值比更高(OR = 2.5,95% CI = 0.9 - 7.1)。基于M2或M4基因型,白人女性吸烟的比值比没有明显差异。
吸烟会增加携带CYP A1 M1变异基因型的女性以及携带CYP1A1 M3变异基因型的非裔美国女性患乳腺癌的风险,但CYP1A1基因型的修饰作用相当微弱。