Effects of glutathione S-transferase A1 (GSTA1) genotype and potential modifiers on breast cancer risk.

Glutathione S-transferases (GSTs) are phase II enzymes that are involved in the detoxification of a wide range of carcinogens. The novel GSTA1*A and GSTA1*B genetic polymorphism results in differential expression, with lower transcriptional activation of GSTA1*B (variant) than that of GSTA1*A (common) allele. Considering that cruciferous vegetables induce GSTs, which metabolize tobacco smoke carcinogens, we hypothesized that the variant GSTA1*B genotype may predispose women to breast cancer, particularly among low cruciferous vegetable consumers and among smokers. Thus, we evaluated potential relationships between GSTA1 polymorphisms and breast cancer risk, in relation to vegetable consumption and smoking status in the Long Island Breast Cancer Study Project (1996-1997), a population-based case-control study. Genotyping (1036 cases and 1089 controls) was performed, and putative breast cancer risk factors and usual dietary intakes were assessed. Having GSTA1*A/*B or *B/*B genotypes was not associated with increased breast cancer risk, compared to having the common *A/*A genotype. However, among women in the lowest two tertiles of cruciferous vegetable consumption, *B/*B genotypes were associated with increased risk (OR (95% CI)=1.73 (1.10-2.72) for 0-1 servings/week), compared to women with *A/*A genotypes. Among women with *B/*B genotypes, a significant inverse trend between cruciferous vegetable consumption and breast cancer risk was observed (P for trend=0.05), and higher consumption (4+ servings/week) ameliorated the increased risk associated with the genotype. Current smokers with *B/*B genotypes had a 1.89-fold increase in risk (OR (95% CI)=1.89 (1.09-3.25)), compared with never smokers with *A/*A genotypes. These data indicate that GSTA1 genotypes related to reduced GSTA1 expression are associated with increased breast cancer primarily among women with lower consumption of cruciferous vegetables and among current smokers.

[1]  C. Verlinde,et al.  Estradiol metabolites as isoform-specific inhibitors of human glutathione S-transferases. , 2004, Chemico-biological interactions.

[2]  Yuesheng Zhang Cancer-preventive isothiocyanates: measurement of human exposure and mechanism of action. , 2004, Mutation research.

[3]  P. Wark,et al.  Habitual consumption of fruits and vegetables: associations with human rectal glutathione S-transferase. , 2004, Carcinogenesis.

[4]  A. Neugut,et al.  Environmental tobacco smoke and breast cancer incidence. , 2004, Environmental research.

[5]  G. Williamson,et al.  Interactions between sulforaphane and apigenin in the induction of UGT1A1 and GSTA1 in CaCo-2 cells. , 2004, Carcinogenesis.

[6]  A. Neugut,et al.  Fruits, vegetables, and micronutrients in relation to breast cancer modified by menopause and hormone receptor status. , 2004, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[7]  J. Freudenheim,et al.  Breast cancer risk in premenopausal women is inversely associated with consumption of broccoli, a source of isothiocyanates, but is not modified by GST genotype. , 2004, The Journal of nutrition.

[8]  C. la Vecchia,et al.  A pooled analysis of case–control studies of thyroid cancer: cigarette smoking and consumption of alcohol, coffee, and tea , 2003, Cancer Causes & Control.

[9]  L. Hutchins,et al.  Association between a glutathione S‐transferase A1 promoter polymorphism and survival after breast cancer treatment , 2003, International journal of cancer.

[10]  C. la Vecchia,et al.  A pooled analysis of case–control studies of thyroid cancer. VII. Cruciferous and other vegetables (International) , 2002, Cancer Causes & Control.

[11]  A. Neugut,et al.  Environmental toxins and breast cancer on Long Island. I. Polycyclic aromatic hydrocarbon DNA adducts. , 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[12]  C. Wolf,et al.  Loss of the Nrf2 transcription factor causes a marked reduction in constitutive and inducible expression of the glutathione S-transferase Gsta1, Gsta2, Gstm1, Gstm2, Gstm3 and Gstm4 genes in the livers of male and female mice. , 2002, The Biochemical journal.

[13]  J. Cerhan,et al.  GSTM1 and GSTT1 polymorphisms and postmenopausal breast cancer risk , 2002, Breast Cancer Research and Treatment.

[14]  Mary Beth Terry,et al.  The Long Island Breast Cancer Study Project: Description of a Multi-Institutional Collaboration to Identify Environmental Risk Factors for Breast Cancer , 2002, Breast Cancer Research and Treatment.

[15]  André Guillouzo,et al.  The human glutathione transferase alpha locus: genomic organization of the gene cluster and functional characterization of the genetic polymorphism in the hGSTA1 promoter. , 2002, Pharmacogenetics.

[16]  C. Sweeney,et al.  The role of human glutathione S-transferases (hGSTs) in the detoxification of the food-derived carcinogen metabolite N-acetoxy-PhIP, and the effect of a polymorphism in hGSTA1 on colorectal cancer risk. , 2001, Mutation research.

[17]  R. Mehta,et al.  Cruciferous Vegetables and Cancer Prevention , 2001, Nutrition and cancer.

[18]  M. Spitz,et al.  Dietary intake of isothiocyanates: evidence of a joint effect with glutathione S-transferase polymorphisms in lung cancer risk. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[19]  G. Coetzee,et al.  Isothiocyanates, glutathione S-transferase M1 and T1 polymorphisms, and lung-cancer risk: a prospective study of men in Shanghai, China , 2000, The Lancet.

[20]  J. Lussier,et al.  High Expression of Bovine α Glutathione S-Transferase (GSTA1, GSTA2) Subunits Is Mainly Associated with Steroidogenically Active Cells and Regulated by Gonadotropins in Bovine Ovarian Follicles. , 1999, Endocrinology.

[21]  J. Witte,et al.  Glutathione transferase null genotype, broccoli, and lower prevalence of colorectal adenomas. , 1998, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[22]  T. Rebbeck Molecular epidemiology of the human glutathione S-transferase genotypes GSTM1 and GSTT1 in cancer susceptibility. , 1997, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[23]  J. Foekens,et al.  Response to adjuvant chemotherapy in primary breast cancer: no correlation with expression of glutathione S-transferases. , 1993, British Journal of Cancer.

[24]  K. El-Bayoumy Environmental carcinogens that may be involved in human breast cancer etiology. , 1992, Chemical research in toxicology.

[25]  B. Mannervik,et al.  Further characterization of hormonal regulation of glutathione transferase in rat liver and adrenal glands. Sex differences and demonstration that growth hormone regulates the hepatic levels. , 1992, The Biochemical journal.

[26]  W. Pearson,et al.  Nomenclature for human glutathione transferases. , 1992, The Biochemical journal.

[27]  D. Hosmer,et al.  Applied Logistic Regression , 1991 .

[28]  A. Harris,et al.  Expression of glutathione S-transferases and cytochrome P450 in normal and tumor breast tissue. , 1990, Carcinogenesis.

[29]  J. Hankin,et al.  Diet and breast cancer: a review. , 1978, The American journal of clinical nutrition.

[30]  Joseph Waksberg,et al.  Sampling Methods for Random Digit Dialing , 1978 .

[31]  B. Green,et al.  Evidence for the presence of mutagenic arylamines in human breast milk and DNA adducts in exfoliated breast ductal epithelial cells , 2002, Environmental and molecular mutagenesis.

[32]  Collaborative Group on Hormonal Factors in Breast Cancer Alcohol, tobacco and breast cancer – collaborative reanalysis of individual data from 53 epidemiological studies, including 58 515 women with breast cancer and 95 067 women without the disease , 2002 .

[33]  B. Mannervik,et al.  Intterindividual variability of glutathione transferase expression , 2001 .

[34]  P. Shields,et al.  Smoking as a Risk Factor for Breast Cancer , 1999 .

[35]  J. Depierre,et al.  Expression of glutathione transferase isoenzymes in the porcine ovary in relationship to follicular maturation and luteinization. , 1999, Chemico-biological interactions.

[36]  R J Carroll,et al.  Comparison of the 60- and 100-item NCI-block questionnaires with validation data. , 1999, Nutrition and cancer.

[37]  J. Lussier,et al.  High expression of bovine alpha glutathione S-transferase (GSTA1, GSTA2) subunits is mainly associated with steroidogenically active cells and regulated by gonadotropins in bovine ovarian follicles. , 1999, Endocrinology.

[38]  A. Bowcock Breast cancer : molecular genetics, pathogenesis, and therapeutics , 1999 .