Tang Jingyuan, Qin Zhiqiang, Li Xiao, Han Peng, Wang Feng, Yang Chengdi, Li Ran, Wang Kunpeng, Tang Min, Wang Wei, Lv Qiang, Zhang Wei
Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210009, China.
Department of Urology, Wuxi Second People's Hospital, Nanjing Medical University, Wuxi, 214002, China.
Oncotarget. 2017 Jul 25;8(30):50034-50050. doi: 10.18632/oncotarget.17293.
The aim of the meta-analysis was to clarify the associations between vascular endothelial growth factor (VEGF) polymorphisms and the risk and prognosis of renal cell carcinoma (RCC). A meta-analysis was performed by searching the databases PubMed, EMBASE and Web of Science for the relevant available studies until August 1st, 2016, and fourteen studies met the inclusion criteria. The pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to evaluate the strength of such associations. Besides, the pooled hazard ratios (HRs) with 95% CIs were used to evaluate the overall survival (OS). Fixed- or random-effects models were conducted according to existence of heterogeneity. Publication bias was evaluated using Begg's funnel plots and Egger's regression test. Overall, this meta-analysis included a total of 8,275 patients, who had been accrued between November 2002 and September 2015. Meta-analysis indicated that -2578C/A, +936C/T and +405G/C polymorphisms in the VEGF gene correlated with elevated RCC risk, especially in Asian populations. Moreover, VEGF -1154G/A and -634C/G polymorphisms were found significantly associated with poor OS of RCC. Therefore, this meta-analysis revealed that VEGF -2578C/A, +936C/T, +405G/C polymorphisms were associated with an elevated susceptibility to RCC, indicating that these three polymorphisms might be risk factors for RCC, especially in Asian populations.
这项荟萃分析的目的是阐明血管内皮生长因子(VEGF)基因多态性与肾细胞癌(RCC)风险及预后之间的关联。通过检索PubMed、EMBASE和Web of Science数据库,查找截至2016年8月1日的相关可用研究,进行了一项荟萃分析,共有14项研究符合纳入标准。计算合并比值比(OR)及其95%置信区间(CI),以评估这种关联的强度。此外,使用合并风险比(HR)及其95%CI评估总生存期(OS)。根据异质性的存在情况采用固定效应或随机效应模型。使用Begg漏斗图和Egger回归检验评估发表偏倚。总体而言,这项荟萃分析共纳入了8275例患者,这些患者于2002年11月至2015年9月期间入组。荟萃分析表明,VEGF基因中的-2578C/A、+936C/T和+405G/C多态性与RCC风险升高相关,尤其是在亚洲人群中。此外,发现VEGF -1154G/A和-634C/G多态性与RCC的不良OS显著相关。因此,这项荟萃分析表明,VEGF -2578C/A、+936C/T、+405G/C多态性与RCC易感性升高相关,表明这三种多态性可能是RCC的危险因素,尤其是在亚洲人群中。