Saadat I, Saadat M
Department of Biology, College of Sciences, Shiraz University, Shiraz 71454, Iran.
Cancer Lett. 2001 Aug 10;169(1):21-6. doi: 10.1016/s0304-3835(01)00550-x.
Several polymorphic glutathione S-transferase (GST) enzymes are involved in the detoxification of active metabolites of many potential carcinogens and may therefore be important in modulating susceptibility to cancers. GSTM1 and GSTT1 are polymorphic, and the null alleles result in a lack of corresponding enzyme activities. Previous studies demonstrated that the GSTM1 and GSTT1 null genotypes correlated with an increased risk of developing some cancers. In this study, we determined GSTM1 and GSTT1 polymorphisms in a population of 131 healthy controls from the south of Iran, 46 patients with colorectal cancers, and 42 patients with gastric cancer. The gastric cancer risk statistically increased due to the GSTM1 null genotype (odds ratio (OR)=2.3, 95% confidence interval (CI): 1.15--4.95). On the other hand, the GSTT1 null genotype in gastric cancer and null genotypes of GSTM1 and GSTT1 in colorectal cancer were not statistically significant. Moreover, individuals showing the GSTM1 and GSTT1 null genotypes might exhibit a greater predisposition to gastric (OR=3.31, 95% CI: 1.14--9.57) and colorectal (OR=2.73, 95% CI: 0.94--7.95, P=0.07) cancers.
几种多态性谷胱甘肽S-转移酶(GST)参与了许多潜在致癌物活性代谢产物的解毒过程,因此在调节癌症易感性方面可能很重要。GSTM1和GSTT1具有多态性,其无效等位基因会导致相应酶活性的缺乏。先前的研究表明,GSTM1和GSTT1无效基因型与某些癌症发生风险的增加相关。在本研究中,我们测定了来自伊朗南部的131名健康对照者、46名结直肠癌患者和42名胃癌患者群体中的GSTM1和GSTT1多态性。由于GSTM1无效基因型,胃癌风险在统计学上增加(优势比(OR)=2.3,95%置信区间(CI):1.15--4.95)。另一方面,胃癌中的GSTT1无效基因型以及结直肠癌中的GSTM1和GSTT1无效基因型在统计学上并不显著。此外,表现出GSTM1和GSTT1无效基因型的个体可能对胃癌(OR=3.31,95%CI:1.14--9.57)和结直肠癌(OR=2.73,95%CI:0.94--7.95,P=0.07)具有更大的易感性。