Xu Zhong, Zhang Lingling, Cao Hui, Bai Banjun
Department of Gastroenterology, Guizhou Provincial People's Hospital, The Affiliated People's Hospital of Guiyang Medical University, Guiyang, 550002, Guizhou Province, PR China.
Department of Oncology, Guizhou Provincial People's Hospital, The Affiliated People's Hospital of Guiyang Medical University, Guiyang, 550002, Guizhou Province, PR of China.
BMC Med Genet. 2014 Oct 20;15:117. doi: 10.1186/s12881-014-0117-2.
Evidence has shown that single nucleotide polymorphism located in pre-miRNA or mature microRNA may modify various biological processes and affect the processing of carcinogenesis. Published results about the association between miR-146a rs2910164 G/C polymorphism and human gastric cancer susceptibility are inconclusive. The aim of this study was to acquire a more precise effect of the association between the miR-146a rs2910164 polymorphism and gastric risk by meta-analysis.
Eligible genetic association studies were searched from PubMed, Web of Knowledge and Chinese Biomedicine Database on human subject. Quantitative data synthesis was conducted for the associations of miR-146a rs2910164 G/C polymorphism with susceptibility to gastric cancer.
Nine eligible studies that included a total of 3,885 gastric cancer patients and 5,396 controls were identified in the present meta-analysis. The overall OR indicated a potential association between rs2910164 polymorphism and GC but the effect was not statistically significant (GG vs.
CG/CC: OR = 1.076, 95% CI 0.925-1.251, P = 0.342). When stratifying for population, the result showed that miR-146a rs2910164 GG genotype was associated with increased gastric cancer risk among Chinese in recessive model (GG vs.
CG/CC: OR = 1.171, 95% CI 1.050-1.306, P = 0.005). Besides, no significant difference was found in gender, smoking, location, metastasis of lymph node and Laurèn's classification.
The present meta-analysis suggests an increased risk between miR-146a rs2910164 GG genotype and gastric cancer susceptibility in Chinese based on published literatures.
有证据表明,位于前体微小RNA或成熟微小RNA中的单核苷酸多态性可能会改变各种生物学过程,并影响癌症发生的进程。已发表的关于miR-146a rs2910164 G/C多态性与人类胃癌易感性之间关联的结果尚无定论。本研究的目的是通过荟萃分析更精确地了解miR-146a rs2910164多态性与胃癌风险之间关联的效应。
从PubMed、Web of Knowledge和中国生物医学数据库中检索关于人类受试者的合格基因关联研究。对miR-146a rs2910164 G/C多态性与胃癌易感性的关联进行定量数据合成。
在本荟萃分析中,确定了9项合格研究,共纳入3885例胃癌患者和5396例对照。总体比值比表明rs2910164多态性与胃癌之间可能存在关联,但效应无统计学意义(GG与CG/CC比较:OR = 1.076,95%CI 0.925 - 1.251,P = 0.342)。按人群分层时,结果显示在隐性模型中,miR-146a rs2910164 GG基因型与中国人群胃癌风险增加相关(GG与CG/CC比较:OR = 1.171,95%CI 1.050 - 1.306,P = 0.005)。此外,在性别、吸烟、肿瘤位置、淋巴结转移和Laurèn分类方面未发现显著差异。
本荟萃分析表明,基于已发表的文献,miR-146a rs2910164 GG基因型与中国人群胃癌易感性之间存在风险增加的关联。