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Carcinogenesis Advance Access published online on July 4, 2003

Carcinogenesis, doi:10.1093/carcin/bgg114
© 2003 by Oxford University Press
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© 2003 Oxford University Press

MOLECULAR EPIDEMIOLOGY AND CANCER PREVENTION

Cytochrome P450 1B1 gene polymorphisms and postmenopausal breast cancer risk

Tove Rylander-Rudqvist 1*, Sara Wedrén 2, Fredrik Granath 2, Keith Humphreys 2, Susanne Ahlberg 1, Elisabete Weiderpass 3, Mikael Oscarson 1, Magnus Ingelman-Sundberg 1, and Ingemar Persson 4

1 Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, SE-171 77 Stockholm, Sweden
2 Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, SE-171 77 Stockholm, Sweden
3 Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, SE-171 77 Stockholm, Sweden; International Agency for Research on Cancer, Lyon, France
4 Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, SE-171 77 Stockholm, Sweden; Swedish Medical Products Agency, Uppsala, Sweden

* Corresponding author. E-mail: tove.rylander{at}imm.ki.se.

Received 6 May 2003 ; revised 18 June 2003 ; accepted 24 June 2003

Abstract

Cytochrome P450 1B1 (CYP1B1) is active in the metabolism of estrogens to reactive catechols and of different procarcinogens. Several studies have investigated the relationship between genetic polymorphisms of CYP1B1 and breast cancer risk, however, with inconsistent results. We investigated such an association in postmenopausal Swedish women, with special emphasis on long-term menopausal hormone users, in a large population-based case-control study. We genotyped 1 521 cases and 1 498 controls for the CYP1B1 SNPs m2, m3 and m4 and reconstructed haplotypes. The frequencies of CYP1B1*1, CYP1B1*2, CYP1B1*3 and CYP1B1*4 alleles among controls were estimated to be 0.087, 0.293, 0.444 and 0.175 respectively. It thus appeared that very few haplotypes contained combinations of SNPs at two or three loci and that single SNP genotype data effectively represented haplotypes. Odds ratios (OR) and 95 percent confidence intervals (CI) were calculated from logistic regression models. We found no overall association between any CYP1B1 genotype and breast cancer risk. The data indicated, however, that women who had used menopausal hormones for four years or longer, and carried the CYP1B1*3/*3 genotype may be at increased risk of breast cancer, OR 2.0 (95% CI 1.1-3.5), compared to long-term users without this genotype. We explored the effect of CYP1B1 genotype on breast cancer risk in subgroups defined by body mass index, family history, smoking and Catechol-O-methyl transferase genotype, but found no convincing evidence for interaction. In summary, our results strongly indicate that the studied CYP1B1 gene polymorphisms do not influence breast cancer risk overall but may modify the risk after long-term menopausal hormone use.

haplotype reconstruction, menopausal hormone use, DASH, minisequencing
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