Abstract
To test the hypothesis that individual susceptibility to carcinogen exposure is a risk factor for breast cancer, we measured DNA adduct formation in normal breast tissues treated in vitro with 4 micro M benzo(a)pyrene in 76 cancer cases and 60 noncancer controls. We found a significantly higher level of adducts (134.6 +/- 21.2/10(9)) among cases compared with controls (66.9 +/- 7.5; P = 0.007). The level of adducts was significantly associated with the risk of breast cancer (odds ratio, 4.38; 95% confidence interval, 1.04 to 18.50; P = 0.044) after adjusting for confounders. Stratified analysis and regression analysis demonstrated that race, pack-years of smoking, family history of breast cancer, and CYP1B1 genotype were significant predictors of the level of benzo(a)pyrene-induced adducts in the breast tissues. These observations suggest that genetic susceptibility to carcinogen exposure may play an important role in breast carcinogenesis.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adult
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Aryl Hydrocarbon Hydroxylases*
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Benzo(a)pyrene / metabolism
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Benzo(a)pyrene / toxicity*
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Breast Neoplasms / chemically induced*
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Breast Neoplasms / genetics*
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Breast Neoplasms / metabolism
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Case-Control Studies
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Cocarcinogenesis*
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Cytochrome P-450 CYP1A1 / genetics
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Cytochrome P-450 CYP1A1 / metabolism
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Cytochrome P-450 CYP1B1
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Cytochrome P-450 Enzyme System / genetics
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Cytochrome P-450 Enzyme System / metabolism
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DNA / drug effects
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DNA / metabolism
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DNA Adducts / metabolism
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Environmental Exposure
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Environmental Pollutants / adverse effects
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Female
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Genetic Predisposition to Disease
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Glutathione Transferase / genetics
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Glutathione Transferase / metabolism
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Humans
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Middle Aged
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Risk Factors
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Smoking / adverse effects
Substances
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DNA Adducts
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Environmental Pollutants
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benzo(a)pyrene-DNA adduct
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Benzo(a)pyrene
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DNA
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Cytochrome P-450 Enzyme System
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Aryl Hydrocarbon Hydroxylases
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CYP1B1 protein, human
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Cytochrome P-450 CYP1A1
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Cytochrome P-450 CYP1B1
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Glutathione Transferase
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glutathione S-transferase M1