Cytochrome P4501A1 and Glutathione S-Transferase M1 Genotypes as Risk Factors for Prostate Cancer in Japan
Background: The p53 mutation spectrum of prostate cancers developing in Japan indicates a role for environmental factors. This suggests there might be differences in susceptibility due to genetic polymorphisms in metabolic activation enzyme genes. We analyzed genetic polymorphisms of the xenobiotic-...
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Veröffentlicht in: | Japanese journal of clinical oncology 1998-11, Vol.28 (11), p.657-660 |
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Zusammenfassung: | Background: The p53 mutation spectrum of prostate cancers developing in Japan indicates a role for environmental factors. This suggests there might be differences in susceptibility due to genetic polymorphisms in metabolic activation enzyme genes. We analyzed genetic polymorphisms of the xenobiotic-metabolizing enzymes, CYP1A1 and GSTM1. Method: Genotyping of CYP1A1 and GSTM1 was investigated by using allele-specific PCR in 115 prostate cancer (PCa) patients and 204 control patients. Results: The CYP1A1 Val/Val genotype significantly increased the risk for PCa (OR = 2.6; 95% CI = 1.11–6.25) and the Ile/Val genotype showed a similar tendency (OR = 1.4; CI = 0.86–2.29). Individuals with the GSTM1 (0/0) genotype demonstrated a slightly increased risk (OR = 1.3; CI = 0.82–2.04). The combination of the CYP1A1 Val allele and GSTM1 (010) genotype was associated with a higher risk (OR = 2.3; CI = 1.18–4.48) than the CYP1A1 Val allele alone. When cases were analyzed by age at initial diagnosis, the relative risks with both the CYP1A1 Val allele and the GSTM1 (0/0) genotype were higher in the young group than in the old group (CYP1A1; OR = 1.7, CI = 0.89–3.17: GSTM1; OR = 1.6, CI = 0.84–2.99). The frequency of the GSTM1 (0/0) genotype was also higher in patients with advanced stage disease. In stage D, the OR was 1.7 with a CI of 0.93–3.17 and in stages A and B, the OR was 0.8 with a CI of 0.40–1.62. Conclusions: These results suggest that CYP1A1 and GSTM1 polymorphisms are linked to a propensity for PCa development. |
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ISSN: | 0368-2811 1465-3621 |
DOI: | 10.1093/jjco/28.11.657 |