Cargando…
Hsa-miR-196a2 Rs11614913 Polymorphism Contributes to Cancer Susceptibility: Evidence from 15 Case-Control Studies
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...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069063/ https://www.ncbi.nlm.nih.gov/pubmed/21483822 http://dx.doi.org/10.1371/journal.pone.0018108 |
_version_ | 1782201315196141568 |
---|---|
author | Chu, Haiyan Wang, Meilin Shi, Danni Ma, Lan Zhang, Zhizhong Tong, Na Huo, Xinying Wang, Wei Luo, Dewei Gao, Yan Zhang, Zhengdong |
author_facet | Chu, Haiyan Wang, Meilin Shi, Danni Ma, Lan Zhang, Zhizhong Tong, Na Huo, Xinying Wang, Wei Luo, Dewei Gao, Yan Zhang, Zhengdong |
author_sort | Chu, Haiyan |
collection | PubMed |
description | 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, P (heterogeneity) = 0.210) and lung cancer risk (OR = 1.25, 95%CI = 1.06–1.46, P (heterogeneity) = 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, P (heterogeneity) = 0.006). CONCLUSIONS: These findings supported that hsa-miR-196a2 rs11614913 polymorphism may contribute to the susceptibility of cancers. |
format | Text |
id | pubmed-3069063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30690632011-04-11 Hsa-miR-196a2 Rs11614913 Polymorphism Contributes to Cancer Susceptibility: Evidence from 15 Case-Control Studies Chu, Haiyan Wang, Meilin Shi, Danni Ma, Lan Zhang, Zhizhong Tong, Na Huo, Xinying Wang, Wei Luo, Dewei Gao, Yan Zhang, Zhengdong PLoS One Research Article 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, P (heterogeneity) = 0.210) and lung cancer risk (OR = 1.25, 95%CI = 1.06–1.46, P (heterogeneity) = 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, P (heterogeneity) = 0.006). CONCLUSIONS: These findings supported that hsa-miR-196a2 rs11614913 polymorphism may contribute to the susceptibility of cancers. Public Library of Science 2011-03-31 /pmc/articles/PMC3069063/ /pubmed/21483822 http://dx.doi.org/10.1371/journal.pone.0018108 Text en Chu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chu, Haiyan Wang, Meilin Shi, Danni Ma, Lan Zhang, Zhizhong Tong, Na Huo, Xinying Wang, Wei Luo, Dewei Gao, Yan Zhang, Zhengdong Hsa-miR-196a2 Rs11614913 Polymorphism Contributes to Cancer Susceptibility: Evidence from 15 Case-Control Studies |
title | Hsa-miR-196a2 Rs11614913 Polymorphism Contributes to Cancer Susceptibility: Evidence from 15 Case-Control Studies |
title_full | Hsa-miR-196a2 Rs11614913 Polymorphism Contributes to Cancer Susceptibility: Evidence from 15 Case-Control Studies |
title_fullStr | Hsa-miR-196a2 Rs11614913 Polymorphism Contributes to Cancer Susceptibility: Evidence from 15 Case-Control Studies |
title_full_unstemmed | Hsa-miR-196a2 Rs11614913 Polymorphism Contributes to Cancer Susceptibility: Evidence from 15 Case-Control Studies |
title_short | Hsa-miR-196a2 Rs11614913 Polymorphism Contributes to Cancer Susceptibility: Evidence from 15 Case-Control Studies |
title_sort | hsa-mir-196a2 rs11614913 polymorphism contributes to cancer susceptibility: evidence from 15 case-control studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069063/ https://www.ncbi.nlm.nih.gov/pubmed/21483822 http://dx.doi.org/10.1371/journal.pone.0018108 |
work_keys_str_mv | AT chuhaiyan hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT wangmeilin hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT shidanni hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT malan hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT zhangzhizhong hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT tongna hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT huoxinying hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT wangwei hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT luodewei hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT gaoyan hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies AT zhangzhengdong hsamir196a2rs11614913polymorphismcontributestocancersusceptibilityevidencefrom15casecontrolstudies |