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Hsa-miR-196a2 Rs11614913 多态性与癌症易感性相关:来自 15 项病例对照研究的证据。

Hsa-miR-196a2 Rs11614913 polymorphism contributes to cancer susceptibility: evidence from 15 case-control studies.

机构信息

Jiangsu Key Lab of Cancer Biomarkers, Prevention & Treatment, Cancer Center, Department of Molecular & Genetic Toxicology, School of Public Health, Nanjing Medical University, Nanjing, China.

出版信息

PLoS One. 2011 Mar 31;6(3):e18108. doi: 10.1371/journal.pone.0018108.

DOI:10.1371/journal.pone.0018108
PMID:21483822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3069063/
Abstract

BACKGROUND

MicroRNAs (miRNAs) are a family of endogenous, small and noncoding RNAs that negatively regulate gene expression by suppressing translation or degrading mRNAs. Recently, many studies investigated the association between hsa-miR-196a2 rs11614913 polymorphism and cancer risk, which showed inconclusive results.

METHODOLOGY/PRINCIPAL FINDINGS: We conducted a meta-analysis of 15 studies that included 9,341 cancer cases and 10,569 case-free controls. We assessed the strength of the association, using odds ratios (ORs) with 95% confidence intervals (CIs). Overall, individuals with the TC/CC genotypes were associated with higher cancer risk than those with the TT genotype (OR=1.18, 95% CI=1.03-1.34, P<0.001 for heterogeneity test). In the stratified analyses, we observed that the CC genotype might modulate breast cancer risk (OR=1.11, 95%CI=1.01-1.23, Pheterogeneity=0.210) and lung cancer risk (OR=1.25, 95%CI=1.06-1.46, Pheterogeneity=0.958), comparing with the TC/TT genotype. Moreover, a significantly increased risk was found among Asian populations in a dominant model (TC/CC versus TT, OR=1.24, 95% CI=1.07-1.43, Pheterogeneity=0.006).

CONCLUSIONS

These findings supported that hsa-miR-196a2 rs11614913 polymorphism may contribute to the susceptibility of cancers.

摘要

背景

microRNAs (miRNAs) 是一类内源性、小的、非编码 RNA,通过抑制翻译或降解 mRNA 来负调控基因表达。最近,许多研究调查了 hsa-miR-196a2 rs11614913 多态性与癌症风险之间的关联,但其结果并不一致。

方法/主要发现: 我们对包括 9341 例癌症病例和 10569 例无癌症对照的 15 项研究进行了荟萃分析。我们使用比值比 (OR) 和 95%置信区间 (CI) 来评估关联的强度。总体而言,TC/CC 基因型个体与癌症风险增加相关,与 TT 基因型相比,OR=1.18 (95% CI=1.03-1.34,P<0.001,异质性检验)。在分层分析中,我们观察到 CC 基因型可能调节乳腺癌风险 (OR=1.11,95%CI=1.01-1.23,P 异质性=0.210) 和肺癌风险 (OR=1.25,95%CI=1.06-1.46,P 异质性=0.958),与 TC/TT 基因型相比。此外,在显性模型中,亚洲人群中发现了显著增加的风险 (TC/CC 与 TT 相比,OR=1.24,95% CI=1.07-1.43,P 异质性=0.006)。

结论

这些发现支持 hsa-miR-196a2 rs11614913 多态性可能导致癌症易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d802/3069063/73371a3a9a3c/pone.0018108.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d802/3069063/45e7ee13cb43/pone.0018108.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d802/3069063/3046adece211/pone.0018108.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d802/3069063/73371a3a9a3c/pone.0018108.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d802/3069063/45e7ee13cb43/pone.0018108.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d802/3069063/3046adece211/pone.0018108.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d802/3069063/73371a3a9a3c/pone.0018108.g003.jpg

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