Mittal R D, Srivastava D S L, Mandhani A, Kumar A, Mittal B
Department of Urology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow-226 014, India.
Indian J Cancer. 2004 Jul-Sep;41(3):115-9.
Glutathione-S-transferases (GSTs) are active in the detoxification of wide variety of endogenous or exogenous carcinogens. The genetic polymorphisms of GSTM1 and GSTT1 genes have been studied earlier to evaluate the relative risk of various cancers. AIM, SETTING AND DESIGN: In the present study, we examined the association of the GSTM1 and GSTT1 gene polymorphisms with sporadic prostate cancer patients in north Indian population.
This case control study was undertaken over a period of 24 months and included 103 prostate cancer patients and 117 controls; both patients and controls originated from northern part of India. The GSTT1 and GSTM1 genotypes were identified by multiplex PCR in peripheral blood DNA samples.
Difference in genotype prevalence and association between case and control group were assessed by the Chi square and Fisher Exact tests.
Frequencies of null genotypes in GSTT1 and GSTM1, was 11% (13/117) and 30% (35/117) respectively in control individuals. The frequencies of GSTT1 and GSTM1 null genotypes in prostate cancer patients were 34% (35/103) and 53% (55/103) respectively.
Our study demonstrates that the null genotypes of GSTT1 and GSTM1 are substantially at higher risk for prostate carcinoma as compared to the normal healthy controls. The GSTT1 and GSTM1 null genotypes did not show significant association with tobacco usage in prostate cancer patients. However, the null genotypes were significantly stratified in 50-60 year-old patients when incidence of prostate cancer is high.
谷胱甘肽 - S - 转移酶(GSTs)在多种内源性或外源性致癌物的解毒过程中发挥作用。此前已对GSTM1和GSTT1基因的遗传多态性进行研究,以评估各种癌症的相对风险。目的、研究地点和设计:在本研究中,我们检测了印度北部人群中散发性前列腺癌患者与GSTM1和GSTT1基因多态性的关联。
本病例对照研究历时24个月,纳入103例前列腺癌患者和117例对照;患者和对照均来自印度北部。通过多重PCR在外周血DNA样本中鉴定GSTT1和GSTM1基因型。
通过卡方检验和Fisher精确检验评估基因型患病率的差异以及病例组与对照组之间的关联。
对照组个体中,GSTT1和GSTM1基因缺失基因型的频率分别为11%(13/117)和30%(35/117)。前列腺癌患者中GSTT1和GSTM1基因缺失基因型的频率分别为34%(35/103)和53%(55/103)。
我们的研究表明,与正常健康对照相比,GSTT1和GSTM1基因缺失基因型患前列腺癌的风险显著更高。GSTT1和GSTM1基因缺失基因型在前列腺癌患者中与烟草使用未显示出显著关联。然而,在前列腺癌发病率较高的50 - 60岁患者中,基因缺失基因型有显著分层。