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谷胱甘肽转移酶M1和P1的基因型及其对肺DNA加合物水平和癌症风险的意义。

Genotypes of glutathione transferase M1 and P1 and their significance for lung DNA adduct levels and cancer risk.

作者信息

Ryberg D, Skaug V, Hewer A, Phillips D H, Harries L W, Wolf C R, Ogreid D, Ulvik A, Vu P, Haugen A

机构信息

Department of Toxicology, National Institute of Occupational Health, Oslo, Norway.

出版信息

Carcinogenesis. 1997 Jul;18(7):1285-9. doi: 10.1093/carcin/18.7.1285.

Abstract

The A-G polymorphism at codon 104 in the glutathione S-transferase P1 (GSTP1) gene was examined in 138 male lung cancer patients and 297 healthy controls. The patients had significantly higher frequency of the GG genotype (15.9%) and a lower frequency of AA (38.4%) than the controls (9.1% and 51.5%, respectively). The level of hydrophobic DNA-adducts were determined in lung tissue from 70 current smokers. Patients with the GG genotype had a significantly higher adduct level than patients with AA (15.5 +/- 10.2 vs 7.9 +/- 5.1 per 10(8) nucleotides, P = 0.006). We also analyzed the deletion polymorphism in the GSTM1 gene in 135 male patients and 342 controls. The patients were stratified according to histology, smoking dose, age, adduct level and mutational types found in the tumors (Ki-ras and p53 genes). The results consistently indicated that the GSTM1 null genotype was associated with a slightly increased lung cancer risk. When the combined GST M1 and P1 genotypes were examined, patients with the combination null and AG or GG had significantly higher adduct levels than all other genotype combinations (P = 0.011). The distribution of combined genotypes was also significantly different in cases and controls, mainly due to increased frequency of the combination GSTM1 null and GSTP1 AG or GG among patients.

摘要

在138例男性肺癌患者和297例健康对照者中检测了谷胱甘肽S-转移酶P1(GSTP1)基因第104密码子处的A-G多态性。患者中GG基因型的频率(15.9%)显著高于对照组(9.1%),而AA基因型的频率(38.4%)低于对照组(51.5%)。测定了70例现吸烟者肺组织中疏水性DNA加合物的水平。GG基因型的患者加合物水平显著高于AA基因型的患者(每10⁸个核苷酸分别为15.5±10.2和7.9±5.1,P = 0.006)。我们还分析了135例男性患者和342例对照者中GSTM1基因的缺失多态性。根据肿瘤(Ki-ras和p53基因)的组织学类型、吸烟量、年龄、加合物水平和突变类型对患者进行分层。结果一致表明,GSTM1基因缺失型与肺癌风险略有增加相关。当检测GSTM1和P1基因的联合基因型时,基因缺失与AG或GG联合的患者加合物水平显著高于所有其他基因型组合(P = 0.011)。病例组和对照组中联合基因型的分布也有显著差异,主要是由于患者中GSTM1基因缺失与GSTP1基因AG或GG联合的频率增加。

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