Sharma A, Mishra A, Das B C, Sardana S, Sharma J K
Division of Molecular Genetics, Institute of Cytology and Preventive Oncology, ICMR, I-7, NOIDA-201301, Uttar Pradesh, India.
Neoplasma. 2006;53(4):309-15.
GSTs are phase II enzymes which are involved in the detoxification of active metabolites of many potential carcinogens from tobacco smoke and therefore may play an important role in modulating susceptibility to tobacco related cancers. This study evaluates the influence of genetic polymorphisms of GSTM1 and GSTT1 gene loci on susceptibility to oral cancer. The genotyping was based on multiplex PCR assay that identified the GSTM1 and GSTT1 null (-/-) genotypes but didn't distinguish homozygous wild type+/+ and heterozygous +/- individuals. Genomic DNA was isolated from cases with oral cancer (n=40) and normal controls (n=87). The prevalence of the GSTM1 null genotypes was 29/87 (33.3%) and 21/40 (52.5%) in controls and oral cancer cases, respectively but the differences were not significant (OR=2.2; 95%CI=0.96-5.1; p=0.06). The frequency of homozygous GSTT1 null genotype in cancer cases was 17/40 (42.5%) as compared to 13/87 (14.94%) in controls and the differences were highly significant (OR=4.2; 95%CI=1.64-10.9; p=0.0002). Oral cancer cases had higher proportion of both GSTM1 and GSTT1 null genotypes as compared to controls but the differences were not statistically significant (OR=2.9; 95%CI=0.71-11.9; p=0.17). When individuals were categorized into two groups, no differences were observed for GSTM1 null genotype frequencies in control and cancer cases (OR=2.9; 95%CI=0.9-9.6; p=0.08) (OR=1.6; 95%CI=0.44-6.1; p=0.58) in <=50 yrs and >50 yrs of age groups. Significant differences between control and cancer cases were observed for GSTT1 null genotypes both in <=50 yrs and >50 yrs of age groups (OR=4.0; 95%CI=1.1-15.0; p=0.03) (OR=4.5; 95%CI=0.97-22.29; p=0.05), respectively. The effect of smoking on GSTM1 null individuals was not found significant (OR=1.0; 95%CI=0.19-4.86; p=0.75) but it was significant in case of GSTT1 null individuals (OR=6.33; 95%CI=1.0-44.1; p=0.02). Our results thus suggest that GSTT1 gene polymorphisms modulate susceptibility to tobacco-related cancer of the oral cavity.
谷胱甘肽S-转移酶(GSTs)是II期酶,参与对烟草烟雾中许多潜在致癌物的活性代谢产物进行解毒,因此可能在调节对烟草相关癌症的易感性方面发挥重要作用。本研究评估了GSTM1和GSTT1基因位点的基因多态性对口腔癌易感性的影响。基因分型基于多重PCR检测,该检测可鉴定GSTM1和GSTT1无效(-/-)基因型,但无法区分纯合野生型+/+和杂合子+/-个体。从口腔癌患者(n=40)和正常对照(n=87)中分离基因组DNA。对照组和口腔癌患者中GSTM1无效基因型的患病率分别为29/87(33.3%)和21/40(52.5%),但差异不显著(比值比[OR]=2.2;95%置信区间[CI]=0.96-5.1;p=0.06)。癌症患者中纯合GSTT1无效基因型的频率为17/40(42.5%),而对照组为13/87(14.94%),差异非常显著(OR=4.2;95%CI=1.64-10.9;p=0.0002)。与对照组相比,口腔癌患者中GSTM1和GSTT1无效基因型的比例更高,但差异无统计学意义(OR=2.9;95%CI=0.71-11.9;p=0.17)。当个体分为两组时,在年龄≤50岁和>50岁的组中,对照组和癌症患者的GSTM1无效基因型频率无差异(OR=2.9;95%CI=0.9-9.6;p=0.08)(OR=1.6;95%CI=0.44-6.1;p=0.58)。在年龄≤50岁和>50岁的组中,对照组和癌症患者的GSTT1无效基因型均存在显著差异(OR=4.0;95%CI=1.1-15.0;p=0.03)(OR=4.5;95%CI=0.97-22.29;p=0.05)。未发现吸烟对GSTM1无效个体有显著影响(OR=1.0;95%CI=0.19-4.86;p=0.75),但对GSTT1无效个体有显著影响(OR=6.33;95%CI=1.0-44.1;p=0.02)。因此,我们的结果表明,GSTT1基因多态性调节对口腔烟草相关癌症的易感性。