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Hsa-miR-196a2 Rs11614913 polymorphism contributes to cancer susceptibility: evidence from 15 case-control studies
Haiyan Chu1, Meilin Wang, Danni Shi
1Jiangsu Key Lab of Cancer Biomarkers, Prevention & Treatment, Cancer Center, Department of Molecular & Genetic Toxicology, School of Public Health, Nanjing Medical University, Nanjing, China.
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.
Insights
The hsa-miR-196a2 rs11614913 polymorphism is linked to increased cancer risk. This genetic variation may influence susceptibility, particularly for breast and lung cancers in Asian populations.
Area of Science:
- Genetics
- Molecular Biology
- Oncology
Background:
- MicroRNAs (miRNAs) are small, noncoding RNAs that regulate gene expression.
- The hsa-miR-196a2 rs11614913 polymorphism has been investigated for its association with cancer risk, yielding inconclusive results.
- Understanding miRNA gene variations is crucial for cancer susceptibility research.
Purpose of the Study:
- To conduct a meta-analysis to clarify the association between the hsa-miR-196a2 rs11614913 polymorphism and cancer risk.
- To evaluate the potential role of this polymorphism in modulating the risk of specific cancer types.
- To investigate population-specific risks associated with the hsa-miR-196a2 rs11614913 polymorphism.
Main Methods:
- Meta-analysis of 15 studies involving 9,341 cancer cases and 10,569 controls.
- Statistical assessment using odds ratios (ORs) with 95% confidence intervals (CIs).
- Stratified analyses were performed to examine associations with specific cancer types and ethnic groups.
Main Results:
- The TC/CC genotypes of hsa-miR-196a2 rs11614913 were associated with a significantly higher overall cancer risk (OR=1.18).
- The CC genotype showed a potential association with increased breast cancer risk (OR=1.11) and lung cancer risk (OR=1.25).
- A significantly increased cancer risk was observed among Asian populations in a dominant model (OR=1.24).
Conclusions:
- The hsa-miR-196a2 rs11614913 polymorphism is a potential contributing factor to cancer susceptibility.
- This genetic variation may play a role in the development of specific cancers like breast and lung cancer.
- Further research is warranted to elucidate the precise mechanisms linking this polymorphism to cancer.
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