CYP1B1 and CYP19 gene polymorphisms and breast cancer incidence: no association in the ARIC study

被引:32
作者
Thyagarajan, B
Brott, M
Mink, P
Folsom, AR
Anderson, KE
Oetting, WS
Gross, M
机构
[1] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Publ Hlth, Div Epidemiol, Minneapolis, MN 55454 USA
[3] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[4] Exponent Hlth Grp, Washington, DC 20036 USA
关键词
breast cancer; prospective study; estrogen metabolism; CYP1B1; CYP19;
D O I
10.1016/j.canlet.2003.12.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We conducted a nested case control study of 178 incident breast cancer cases and 356 controls in the Atherosclerosis Risk in Communities study. We evaluated the association between breast cancer and Val432Leu polymorphism in the CYP1B1 gene and the tetranucleotide repeats in intron 4 of the CYP19 gene. After adjustment for height, age at menopause, age at menarche, BMI, HRT, and alcohol intake, carriers of the Val/Leu or Val/Val genotype had a 1.45 fold (95% CI 0.85-2.47) greater odds of breast cancer than Leu/Leu carriers. There was no association of the breast cancer with any individual CYP19 allele. Compared to individuals homozygous with the 167 allele, odds ratios were close to 1.0 for the 167 heterozygous genotype and for the remaining tetranucleotide repeats combined. Our data shows no association between breast cancer and the Leu432Val polymorphism of the CYP1B1 gene or the tetranucleotide repeats of the CYP19 gene. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:183 / 189
页数:7
相关论文
共 31 条
[1]  
Bailey LR, 1998, CANCER RES, V58, P5038
[2]   Polymorphic variation in CYP19 and the risk of breast cancer [J].
Baxter, SW ;
Choong, DYH ;
Eccles, DM ;
Campbell, IG .
CARCINOGENESIS, 2001, 22 (02) :347-349
[3]   A COMPUTER-PROGRAM FOR INCIDENCE DENSITY SAMPLING OF CONTROLS IN CASE-CONTROL STUDIES NESTED WITHIN OCCUPATIONAL COHORT STUDIES [J].
BEAUMONT, JJ ;
STEENLAND, K ;
MINTON, A ;
MEYER, S .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1989, 129 (01) :212-219
[4]  
De Vivo I, 2002, CANCER EPIDEM BIOMAR, V11, P489
[5]  
Haiman CA, 2000, INT J CANCER, V87, P204, DOI 10.1002/1097-0215(20000715)87:2<204::AID-IJC8>3.3.CO
[6]  
2-V
[7]   17 beta-estradiol hydroxylation catalyzed by human cytochrome P450 1B1 [J].
Hayes, CL ;
Spink, DC ;
Spink, BC ;
Cao, JQ ;
Walker, NJ ;
Sutter, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (18) :9776-9781
[8]   Polymorphisms in the human aromatase cytochrome P450 gene (CYP19) and breast cancer risk [J].
Healey, CS ;
Dunning, AM ;
Durocher, F ;
Teare, D ;
Pharoah, PDP ;
Luben, RN ;
Easton, DF ;
Ponder, BAJ .
CARCINOGENESIS, 2000, 21 (02) :189-193
[9]   EPIDEMIOLOGY OF BREAST-CANCER [J].
KELSEY, JL ;
GAMMON, MD .
EPIDEMIOLOGIC REVIEWS, 1990, 12 :228-240
[10]   Metabolism of benzo[a]pyrene and benzo[a]pyrene-7,8-diol by human cytochrome P450 1B1 [J].
Kim, JH ;
Stansbury, KH ;
Walker, NJ ;
Trush, MA ;
Strickland, PT ;
Sutter, TR .
CARCINOGENESIS, 1998, 19 (10) :1847-1853