Song Yipeng, Du Yuanna, Zhou Qi, Ma Jinbo, Yu Jinming, Tao Xiaofeng, Zhang Fenghua
Department of Radiation Oncology, Affiliated Yantai Yuhuangding Hospital, Qingdao University Yantai 264000, China.
Department of Tumor Biological Treatment, The Third Affiliated Hospital, Soochow University Changzhou 213003, Jiangsu Province, China.
Int J Clin Exp Med. 2014 Oct 15;7(10):3215-24. eCollection 2014.
The association of glutathione s-transferase P1 (GSTP1) Ile105Val polymorphism with risk of esophageal cancer (EC) has been evaluated in many studies; however, the results from these studies are controversial. Thus, further analysis on association between GSTP1 Ile105Val polymorphism and risk of EC is needed among a larger study population.
We searched the relevant electronic databases and performed a meta-analysis based on 21 published case-control studies. The Chi-square based I(2)-statistic test was performed to evaluate possible heterogeneity across the studies. Additionally, random-effects models were used to calculate crude pooled odds ratios (ORs) with 95% confidence intervals (CIs).
Overall, this meta-analysis did support a significant association between GSTP1 Ile105Val polymorphism and risk of EC (pooled OR 1.25, 95% CI, 1.05-1.49). Furthermore, the stratified analysis showed that, in comparison to GSTP1 Ile105Val Ile/Ile genotype, the Val/Val genotype was significantly associated with risk of esophageal squamous cell carcinoma (ESCC) (pooled OR 1.45, 95% CI, 1.07-1.96), particularly in the Caucasian population (pooled OR 1.41, 95% CI, 1.01-1.95). Such a significant association was not observed for esophageal adenocarcinoma (EAC) patients or subjects of an Asian ethnicity. Moreover, substantial evidence of heterogeneity among the studies was not observed.
The results from this meta-analysis support a significant association between the GSTP1 Ile105Val polymorphism and risk of EC, particularly in a subgroup with ESCC and in the Caucasian population. Further studies with larger sample sizes are needed to validate our findings.
许多研究评估了谷胱甘肽S-转移酶P1(GSTP1)Ile105Val多态性与食管癌(EC)风险之间的关联;然而,这些研究的结果存在争议。因此,需要在更大的研究人群中进一步分析GSTP1 Ile105Val多态性与EC风险之间的关联。
我们检索了相关电子数据库,并基于21项已发表的病例对照研究进行了荟萃分析。采用基于卡方的I(2)统计检验来评估各研究之间可能存在的异质性。此外,使用随机效应模型计算粗合并比值比(OR)及95%置信区间(CI)。
总体而言,该荟萃分析确实支持GSTP1 Ile105Val多态性与EC风险之间存在显著关联(合并OR为1.25,95%CI为1.05 - 1.49)。此外,分层分析表明,与GSTP1 Ile105Val Ile/Ile基因型相比,Val/Val基因型与食管鳞状细胞癌(ESCC)风险显著相关(合并OR为1.45,95%CI为1.07 - 1.96),特别是在白种人群中(合并OR为1.41,95%CI为1.01 - 1.95)。在食管腺癌(EAC)患者或亚洲种族受试者中未观察到这种显著关联。此外,未观察到各研究之间存在实质性异质性证据。
该荟萃分析的结果支持GSTP1 Ile105Val多态性与EC风险之间存在显著关联,特别是在ESCC亚组和白种人群中。需要进一步开展更大样本量的研究来验证我们的发现。