Tiwari Sonia, Vijayaraghavalu Sivakumar, Kumar Munish
Department of Biochemistry, University of Allahabad, Allahabad, UP-211002, India. Email:
Department of Radiation Oncology, Kamala Nehru Memorial Hospital, Allahabad, UP-211002, India.
Asian Pac J Cancer Prev. 2019 Sep 1;20(9):2707-2714. doi: 10.31557/APJCP.2019.20.9.2707.
Aim: In this case control study involving, 220 human subjects; polymorphisms in xenobiotic metabolizing genes (GST-M1, -T1 and -P1) and their association to lung cancer risk is being analysed among smokers and nonsmokers. GSTM1 or GSTT1 gene polymorphism and amino acid changes in GSTP1 have been correlated and may be associated to lung cancer risk. Other factor includes exposure to environmental pollutants and life style choices. We have explored gene-gene and gene-environment interaction in the aetiology of lung cancer risk among north Indian population. Patients and Methods: For the study we have collected 120 lung cancer patient blood samples from Kamala Nehru Memorial Cancer Hospital, Allahabad, Uttar Pradesh and 100 matched controls. DNA was isolated and GST-M1 and - T1 genotyping were assessed by multiplex PCR whereas the GSTP1 polymorphism was analysed using restriction fragment length polymorphism. The risk of lung carcinogenesis was assessed using logistic regression analysis calculating the odd ratio (OR) with 95% confidence interval (CI). Results: The risk of lung carcinogenesis was three fold higher for null GSTT1 (OR=3.045, 95%CI=1.750-5.301, p-value <0.001) genotype; whereas other two types; GSTM1 (OR= 1.342, 95% CI=0.788-2.284, p-value=0.270) and GSTP1 (OR=0.806, 95% CI=0.526-1.236, p-value=0.323) showed no association to lung cancer susceptibility respectively. Smokers diagnosed with lung cancer had more null genotypes for GSTT1 (OR=4.773, 95%CI=1.939-11.751, p<0.001). The ‘at risk’ genotype combination GSTM1 (null) /GSTT1 (null) (OR=1.76, 95%CI; 0.920-3.370, p-value=0.03) showed increased susceptibility to lung cancer risk. The genotype combination of GSTT1 (null)/GSTP1 (Ile/Ile) (p=0.009) was associated with increased lung cancer risk. Conclusion: The results of this study suggest that; GSTT1 null genotype were more susceptible for lung cancer risk and smoking increases the susceptibility for lung cancer several folds among the North Indian population. Gene-gene interaction for null genotypes of GSTM1 and GSTT1 were correlated with higher risk of having lung cancer.
在这项涉及220名人类受试者的病例对照研究中,正在分析吸烟者和非吸烟者中异生物质代谢基因(GST-M1、-T1和-P1)的多态性及其与肺癌风险的关联。GSTM1或GSTT1基因多态性以及GSTP1中的氨基酸变化已被关联起来,并且可能与肺癌风险相关。其他因素包括接触环境污染物和生活方式选择。我们在北印度人群中探讨了肺癌风险病因中的基因-基因和基因-环境相互作用。
为了该研究,我们从北方邦阿拉哈巴德的卡玛拉·尼赫鲁纪念癌症医院收集了120例肺癌患者的血样以及100例匹配的对照。分离DNA,通过多重PCR评估GST-M1和-T1基因分型,而使用限制性片段长度多态性分析GSTP1多态性。使用逻辑回归分析计算比值比(OR)及其95%置信区间(CI)来评估肺癌发生的风险。
GSTT1基因缺失型(OR=3.045,95%CI=1.750-5.301,p值<0.001)基因型患肺癌的风险高出三倍;而其他两种类型,GSTM1(OR=1.342,95%CI=0.788-2.284,p值=0.270)和GSTP1(OR=0.806,95%CI=0.526-1.236,p值=0.323)分别与肺癌易感性无关联。被诊断为肺癌的吸烟者GSTT1基因缺失型更多(OR=4.773,95%CI=1.939-11.751,p<0.001)。“高危”基因型组合GSTM1(缺失型)/GSTT1(缺失型)(OR=1.76,95%CI;0.920-3.370,p值=0.03)显示出对肺癌风险的易感性增加。GSTT1(缺失型)/GSTP1(异亮氨酸/异亮氨酸)的基因型组合(p=0.009)与肺癌风险增加相关。
本研究结果表明,GSTT1基因缺失型对肺癌风险更易感,并且吸烟使北印度人群中患肺癌的易感性增加数倍。GSTM1和GSTT1基因缺失型的基因-基因相互作用与患肺癌的较高风险相关。