Wang Yafeng, Jiang Heping, Liu Tianyun, Tang Weifeng, Ma Zhiqiang
Department of Cardiology, The People's Hospital of Xishuangbanna Dai Autonomous Prefecture Jinghong, Yunnan Province, China.
Emergency Department, Affiliated Jintan People's Hospital of Jiangsu University Jintan, China.
Int J Clin Exp Med. 2015 Aug 15;8(8):12448-62. eCollection 2015.
The association between cyclooxygenase-2 (COX-2) -1195G>A (rs689466) polymorphism and cancer risk has been extensively explored. However, the results of previous studies remain controversial. To address this gap, we performed an updated meta-analysis of fifty-eight studies involving a total of 50,672 subjects. Searching of PubMed and Embase databases was performed for publications on the association between COX-2 -1195G>A polymorphism and the risk of cancer. Statistical correlation was identified between COX-2 -1195G>A variants and overall cancer risk in five genetic models. In a sub-group analysis based on cancer type, significant association between COX-2 -1195G>A polymorphism and increased risk of gastric cancer, pancreatic cancer, hepatocellular carcinoma and other cancers was found. In a sub-group analysis by ethnicity, increased cancer risk was observed among Asians instead of Caucasians, Africans and mixed populations. Furthermore, in a sub-group analysis based on cancer system, increased cancer risk was found in digestive system cancer and other system cancer. Non-parametric "trim-and-fill" method was harnessed as a sensitivity analysis method and the results suggested our findings reliable. In summary, the results of our meta-analysis highlight that COX-2 -1195G>A polymorphism may be a risk factor for cancer.
环氧化酶-2(COX-2)-1195G>A(rs689466)基因多态性与癌症风险之间的关联已得到广泛研究。然而,以往研究的结果仍存在争议。为填补这一空白,我们对58项研究进行了更新的荟萃分析,共纳入50672名受试者。通过检索PubMed和Embase数据库,查找有关COX-2 -1195G>A基因多态性与癌症风险关联的文献。在五种遗传模型中确定了COX-2 -1195G>A变异与总体癌症风险之间的统计学相关性。在基于癌症类型的亚组分析中,发现COX-2 -1195G>A基因多态性与胃癌、胰腺癌、肝细胞癌及其他癌症风险增加之间存在显著关联。在按种族进行的亚组分析中,亚洲人而非白种人、非洲人和混合人群的癌症风险增加。此外,在基于癌症系统的亚组分析中,消化系统癌症和其他系统癌症的癌症风险增加。采用非参数“修剪填充”方法作为敏感性分析方法,结果表明我们的发现可靠。总之,我们的荟萃分析结果突出表明,COX-2 -1195G>A基因多态性可能是癌症的一个风险因素。