miR-196a2 polymorphisms and susceptibility to cancer: A meta-analysis involving 24,697 subjects

被引:18
|
作者
Wang, Pingyu [1 ]
Xie, Shuyang [2 ]
Cui, Aidong [3 ]
Zhang, Yanxiang [2 ]
Jiang, Baofa [1 ]
机构
[1] Shandong Univ, Sch Publ Hlth, Jinan 250012, Shandong, Peoples R China
[2] Binzhou Med Univ, Yantai, Peoples R China
[3] Weifang Med Coll, Laiyang Cent Hosp, Yantai, Peoples R China
关键词
cancer; hsa-miR-196a2; polymorphism; meta-analysis; COMMON GENETIC-VARIANTS; SQUAMOUS-CELL CARCINOMA; MICRORNA-RELATED GENES; PRE-MICRORNAS; LUNG-CANCER; HEPATOCELLULAR-CARCINOMA; FUNCTIONAL POLYMORPHISM; BREAST-CANCER; ANNEXIN A1; RISK;
D O I
10.3892/etm.2011.399
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
An increasing number of studies have shown that the hsa-miR-196a2 rs11614913 polymorphism occurs in different types of cancer, but the results are generally controversial and inadequate, mainly due to limited statistical power. To resolve this issue, the present meta-analysis was carried out. Databases, including PubMed and Embase, were searched using: (miR-196a2[All Fields] OR rs11614913[All Fields]) AND ('neoplasms'[MeSH Terms] OR 'neoplasms' [All Fields] OR 'cancer'[All Fields]). Crude odds ratios (ORs) with 95% confidence intervals (CIs) were summarized in forest plots and detailed in tables. A total of 20 studies, including 11,004 cases and 13,693 controls, were included in the meta-analysis. The hsa-miR-196a2 rs11614913 polymorphism was significantly associated with an increased cancer risk in all genetic models (CC vs. TT: OR=1.280, 95% CI 1.131-1.449, P<0.001; CT vs. TT: OR=1.187, 95% Cl 1.079-1.306, P<0.001; CC/CT vs. TT: OR=1.216, 95% CI 1.104-1.341, P<0.001; and CC vs. CT/TT: OR=1.115, 95% CI 1.025-1.213, P=0.011). In conclusion, this meta-analysis provides compelling evidence that the hsa-miR-196a2 rs11614913 polymorphism plays a crucial role in the development of cancer. Screening of patients for the hsa-miR-196a2 rs11614913 polymorphism can prove clinically useful for the prediction and prevention of cancer.
引用
收藏
页码:324 / 330
页数:7
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