Pandith Arshad Ahmad, Lateef Adil, Shahnawaz Sheikh, Hussain Aashaq, Malla Tahir Mohiuddin, Azad Niyaz, Shehjar Fahim, Salim Mosin, Shah Zafar Amin
Advanced Centre for Human Genetics, SKIMS, Srinagar, India E-mail :
Asian Pac J Cancer Prev. 2013;14(11):6375-8. doi: 10.7314/apjcp.2013.14.11.6375.
The glutathione S transferase (GST) family of enzymes plays a vital role in the phase II biotransformation of environmental carcinogens, pollutants, drugs and other xenobiotics. GSTs are polymorphic and polymorphisms in GST genes have been associated with cancer susceptibility and prognosis. GSTP1 is associated with risk of various cancers including bladder cancer. A case control study was conducted to determine the genotype distribution of GSTP1 A>G SNP, to elucidate the possible role of this SNP as a risk factor in urinary bladder cancer (UBC) development and to examine its correlation with clinico-pathologic variables inUBC cases.
Using the polymerase chain reaction-restriction fragment length polymorphism (PCR- RFLP) approach, we tested the genotype distribution of 180 bladder cancer patients in comparison with 210 cancer-free controls from the same geographical region with matched frequency in age and gender.
We did not observe significant genotype differences between the control and bladder cancer patients overall with an odds ratio (OR)=1.23 (p>0.05). The rare allele (AG+GG) was found to be present more in cases (28.3%) than in controls (24%), though the association was not significant (p<0.05). However, a significant risk of more than 2-fold was found for the variant allele (AG+GG) with smokers in cases as compared to controls (p>0.05).
Thus, it is evident from our study that GSTP1 SNP is not implicated overall in bladder cancer, but that the rare, valine-related allele is connected with higher susceptibility to bladder cancer in smokers and also males.
谷胱甘肽S转移酶(GST)家族的酶在环境致癌物、污染物、药物及其他外源性物质的Ⅱ相生物转化过程中发挥着至关重要的作用。GST具有多态性,GST基因的多态性与癌症易感性及预后相关。GSTP1与包括膀胱癌在内的多种癌症风险相关。开展了一项病例对照研究,以确定GSTP1 A>G单核苷酸多态性(SNP)的基因型分布,阐明该SNP作为膀胱癌(UBC)发生风险因素的可能作用,并研究其与UBC病例临床病理变量的相关性。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,我们检测了180例膀胱癌患者的基因型分布,并与来自同一地理区域、年龄和性别频率匹配的210名无癌对照进行比较。
总体而言,我们未观察到对照组与膀胱癌患者之间存在显著的基因型差异,优势比(OR)=1.23(p>0.05)。发现病例组中罕见等位基因(AG+GG)的出现频率(28.3%)高于对照组(24%),尽管该关联不显著(p<0.05)。然而,与对照组相比,病例组中吸烟者的变异等位基因(AG+GG)具有超过2倍的显著风险(p>0.05)。
因此,从我们的研究中可以明显看出,GSTP1 SNP总体上与膀胱癌无关,但罕见的、与缬氨酸相关的等位基因与吸烟者及男性患膀胱癌的较高易感性相关。