Sun Wei, Yao Li, Jiang Benchun
Department of General Surgery, Affiliated Shengjing Hospital, China Medical University, Shenyang, 110004, Liaoning Province, China,
Tumour Biol. 2014 Jan;35(1):239-45. doi: 10.1007/s13277-013-1029-z. Epub 2013 Aug 23.
Allelic variant within genes encoding glutathione S-transferase T1 (GSTT1) has been suggested to be a possible risk factor of gastric cancer, but previous studies provide controversial results. This study aimed to assess the effects of GSTT1 polymorphism on gastric cancer by means of meta-analysis. We included published studies on the relationship between GSTT1 null allele and gastric cancer risk after searching electronic databases. A meta-analysis was conducted by calculating the pooled odds ratios (OR) and the 95% confidence intervals (95% CI). Forty-two studies with a total of 8,203 gastric cancer cases and 13,866 controls were included into this meta-analysis. When all 42 studies were pooled into this meta-analysis, there was a significant association between the GSTT1 null allele and gastric cancer risk (OR = 1.24, 95% CI 1.14-1.36, P < 0.00001). Sensitivity analysis by excluding individual studies showed that there was no effect on the pooled OR with 95% CI. After excluding studies with low quality, there was still a significant association between the GSTT1 null allele and gastric cancer risk (OR = 1.24, 95% CI 1.13-1.36, P < 0.00001). In the subgroup analysis, there was a significant association between the GSTT1 null allele and gastric cancer risk in both Europeans and Asians. There was no risk of publication bias in this meta-analysis. Our results suggest that GSTT1 null allele is associated with increased risk of gastric cancer.
编码谷胱甘肽S-转移酶T1(GSTT1)的基因中的等位基因变异被认为可能是胃癌的一个风险因素,但先前的研究结果存在争议。本研究旨在通过荟萃分析评估GSTT1基因多态性对胃癌的影响。我们在检索电子数据库后纳入了已发表的关于GSTT1无效等位基因与胃癌风险关系的研究。通过计算合并比值比(OR)和95%置信区间(95%CI)进行荟萃分析。本荟萃分析纳入了42项研究,共8203例胃癌病例和13866例对照。当将所有42项研究纳入该荟萃分析时,GSTT1无效等位基因与胃癌风险之间存在显著关联(OR = 1.24,95%CI 1.14 - 1.36,P < 0.00001)。通过排除个别研究进行的敏感性分析表明,对合并的OR及95%CI没有影响。排除质量较低的研究后,GSTT1无效等位基因与胃癌风险之间仍存在显著关联(OR = 1.24,95%CI 1.13 - 1.36,P < 0.00001)。在亚组分析中,欧洲人和亚洲人中GSTT1无效等位基因与胃癌风险之间均存在显著关联。该荟萃分析不存在发表偏倚风险。我们的结果表明,GSTT1无效等位基因与胃癌风险增加有关。