Differences in genetic susceptibility to tobacco-induced carcinogenesis appear to modulate an individual's risk of squamous-cell carcinoma of the head and neck (SCCHN). Risk for SCCHN may be associated with the null alleles of the carcinogen-metabolizing genes glutathione-S-transferase (GST) T1 and
Genetic polymorphisms of drug-metabolizing enzymes and susceptibility to head-and-neck squamous-cell carcinoma
โ Scribed by Shunji Morita; Masahiko Yano; Toshimasa Tsujinaka; Yosuke Akiyama; Masaaki Taniguchi; Katsuhiko Kaneko; Hirofumi Miki; Takashi Fujii; Kunitoshi Yoshino; Hideo Kusuoka; Morito Monden
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- French
- Weight
- 51 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
We have investigated the association between the polymorphisms of drug-metabolizing enzymes and susceptibility to head-and-neck squamous-cell carcinoma (HNSCC). PCRbased analysis was performed on 145 Japanese patients and 164 healthy Japanese controls to determine genotypes of polymorphisms in CYP1A1, CYP2E1, GSTM1, GSTP1, and NAT2. Patients and controls were compared by multivariate analysis. The CYP1A1 Val/Val genotype was seen more frequently in patients than in controls [odds ratio (OR) 4.1, p โซุโฌ 0.038). The frequency of the slow plus intermediate NAT2 genotypes was also higher in patients (OR 2.0, p โซุโฌ 0.039). When we analyzed the distributions of the genotypes in 69 laryngeal and 45 pharyngeal cancer patients, laryngeal cancer patients had a higher frequency of NAT2 slow or intermediate genotype (OR 2.7, p โซุโฌ 0.011) and GSTP1 AA genotype (OR 2.4, p โซุโฌ 0.047) than controls. Pharyngeal cancer patients had a higher frequency of the CYP1A1 Val/Val genotype than controls (OR 5.7, p โซุโฌ 0.034), suggesting that different organs may be responsive to different chemicals from the environment. Furthermore, 23 patients who developed multiple cancers (HNSCC plus other) were compared with 115 patients with HNSCC alone. There was no significant difference in the polymorphisms between the 2 groups, though excessive alcohol consumption (more than 50 g/day of ethanol) appeared to be a risk factor for multiple cancers (p โซุโฌ 0.053). Int.
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