The association between two polymorphisms in pre-miRNAs and breast cancer risk: a meta-analysis

被引:84
|
作者
Gao, Lin-Bo [1 ]
Bai, Peng [2 ]
Pan, Xin-Min [2 ,3 ]
Jia, Jing [4 ]
Li, Li-Juan [2 ]
Liang, Wei-Bo [2 ]
Tang, Ming [5 ]
Zhang, Lu-Shun [2 ]
Wei, Yong-Gang [6 ]
Zhang, Lin [1 ]
机构
[1] Sichuan Univ, W China Univ Hosp 2, Lab Mol Translat Med, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, W China Sch Preclin & Forens Med, Dept Forens Biol, Chengdu 610041, Sichuan, Peoples R China
[3] Henan Univ Sci & Technol, Dept Forens Pathol, Luoyang 471003, Henan, Peoples R China
[4] Zhejiang Acad Med Sci, Dept Normal Pharmacol, Hangzhou 310013, Zhejiang, Peoples R China
[5] First Peoples Hosp Yunnan Prov, Dept Pathol, Kunming 650000, Yunnan, Peoples R China
[6] Sichuan Univ, W China Hosp, Dept Gen Surg, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Hsa-miR-146; rs2910164; Has-miR-196a2; rs11614913; Single nucleotide polymorphism; Breast cancer; Meta-analysis; FUNCTIONAL POLYMORPHISM; MIR-146A GENE; EXPRESSION; MICRORNAS;
D O I
10.1007/s10549-010-0993-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Emerging evidence has shown that miRNAs participate in human carcinogenesis as tumor suppressors or oncogenes. Single nucleotide polymorphism (SNP) which located in the pre-miRNA may affect the processing and then influence the expression of mature miRNA. Previous studies yielded conflicting results as to the association of two common polymorphisms in pre-miRNAs (i.e. hsa-miR-146 rs2910164 and hsa-miR-196a2 rs11614913) with breast cancer. To derive a more precise effect on the association between these polymorphisms and breast cancer risk, we conducted a meta-analysis. Through retrieving PubMed for the period up to May 2010, a total of four studies were identified with 3,007 cases and 3,718 controls for has-miR-146a rs2910164 polymorphism and with 3,287 cases and 4,298 controls for hsa-miR-196a2 rs11614913 polymorphism. We found that individuals carrying CC genotype of has-miR-196a2 rs11614913 polymorphism was associated with an increased breast cancer risk in homozygote comparison (OR = 1.30; 95% CI, 1.01-1.68), and dominant model (OR = 1.11; 95% CI, 1.01-1.23). However, no significant association between has-miR-146a rs2910164 polymorphism and breast cancer risk was observed in all comparison models tested. These findings suggest that has-miR-196a2 rs11614913 polymorphism may play crucial roles in breast cancer development.
引用
收藏
页码:571 / 574
页数:4
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