Liu Yuhan, He Anbang, Liu Baoer, Zhong Yucheng, Liao Xinhui, Yang Jiangeng, Chen Jieqing, Wu Jianting, Mei Hongbing
Department of Urology, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen, China.
Department of Urology, Peking University First Hospital, The Institute of Urology, Peking University, National Urological Cancer Centre, Beijing, China.
Onco Targets Ther. 2018 Mar 1;11:1121-1139. doi: 10.2147/OTT.S154211. eCollection 2018.
Several epidemiological studies have reported that polymorphisms in microRNA-196a2 (miR-196a2) were associated with various cancers. However, the results remained unverified and were inconsistent in different cancers. Therefore, we carried out an updated meta-analysis to elaborate the effects of rs11614913 polymorphism on cancer susceptibility. A total of 84 articles with 35,802 cases and 41,541 controls were included to evaluate the association between the miR-196a2 rs11614913 and cancer risk by pooled odds ratios (ORs) and 95% confidence intervals (CIs). The results showed that miR-196a2 rs11614913 polymorphism is associated with cancer susceptibility, especially in lung cancer (homozygote comparison, OR =0.840, 95% CI =0.734-0.961; recessive model, OR =0.858, 95% CI =0.771-0.955), hepatocellular carcinoma (allelic contrast, OR =0.894, 95% CI =0.800-0.998; homozygote comparison, OR =0.900, 95% CI =0.813-0.997; recessive model, OR =0.800, 95% CI =0.678-0.944), and head and neck cancer (allelic contrast, OR =1.076, 95% CI =1.006-1.152; homozygote comparison, OR =1.214, 95% CI =1.043-1.413). In addition, significant association was found among Asian populations (allele model, OR =0.847, 95% CI =0.899-0.997, =0.038; homozygote model, OR =0.878, 95% CI =0.788-0.977, =0.017; recessive model, OR =0.895, 95% CI =0.824-0.972, =0.008) but not in Caucasians. The updated meta-analysis confirmed the previous results that miR-196a2 rs11614913 polymorphism may serve as a risk factor for patients with cancers.
多项流行病学研究报告称,微小RNA-196a2(miR-196a2)中的多态性与多种癌症相关。然而,这些结果仍未得到验证,且在不同癌症中的结果并不一致。因此,我们进行了一项更新的荟萃分析,以阐述rs11614913多态性对癌症易感性的影响。总共纳入了84篇文章,涉及35802例病例和41541例对照,通过合并比值比(OR)和95%置信区间(CI)来评估miR-196a2 rs11614913与癌症风险之间的关联。结果表明,miR-196a2 rs11614913多态性与癌症易感性相关,尤其是在肺癌中(纯合子比较,OR = 0.840,95% CI = 0.734 - 0.961;隐性模型,OR = 0.858,95% CI = 0.771 - 0.955)、肝细胞癌中(等位基因对比,OR = 0.894,95% CI = 0.800 - 0.998;纯合子比较,OR = 0.900,95% CI = 0.813 - 0.997;隐性模型,OR = 0.800,95% CI = 0.678 - 0.944)以及头颈癌中(等位基因对比,OR = 1.076,95% CI = 1.006 - 1.152;纯合子比较,OR = 1.214,95% CI = 1.043 - 1.413)。此外,在亚洲人群中发现了显著关联(等位基因模型,OR = 0.847,95% CI = 0.899 - 0.997,P = 0.038;纯合子模型,OR = 0.878,95% CI = 0.788 - 0.977,P = 0.017;隐性模型,OR = 0.895,95% CI = 0.824 - 0.972,P = 0.008),但在白种人中未发现。更新的荟萃分析证实了先前的结果,即miR-196a2 rs11614913多态性可能是癌症患者的一个风险因素。