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The association between miR-499 polymorphism and cancer susceptibility: a meta-analysis

BACKGROUND: MicroRNAs are a class of new noncoding RNA that play important roles in the pathogenesis of tumor. Rs3746444 in miR-499 is suggested to be associated with cancer susceptibility. In the present study, we assess the association between miR-499 rs3746444 polymorphism and cancer susceptibili...

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Autores principales: Xu, Zhongfei, Zhang, Enjiao, Duan, Weiyi, Sun, Changfu, Bai, Shuang, Tan, Xuexin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550183/
https://www.ncbi.nlm.nih.gov/pubmed/26347202
http://dx.doi.org/10.2147/OTT.S88224
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author Xu, Zhongfei
Zhang, Enjiao
Duan, Weiyi
Sun, Changfu
Bai, Shuang
Tan, Xuexin
author_facet Xu, Zhongfei
Zhang, Enjiao
Duan, Weiyi
Sun, Changfu
Bai, Shuang
Tan, Xuexin
author_sort Xu, Zhongfei
collection PubMed
description BACKGROUND: MicroRNAs are a class of new noncoding RNA that play important roles in the pathogenesis of tumor. Rs3746444 in miR-499 is suggested to be associated with cancer susceptibility. In the present study, we assess the association between miR-499 rs3746444 polymorphism and cancer susceptibility through a meta-analysis. METHODS: We searched relevant articles from the PubMed and Embase databases. We screened all the resulting articles for adherence to the inclusion and exclusion criteria. The associations between miR-499 polymorphism and cancer susceptibility were estimated by computing the odds ratios (ORs) and 95% confidence intervals (CIs). All analyses were performed using Stata software. RESULTS: There are 18 datasets included in the analysis. Statistically significant associations were found between the miR-499 rs3746444 polymorphism and susceptibility to cancer (GG versus AA: OR =1.24, 95% CI: 1.01–1.52; G versus A: OR =1.11, 95% CI: 1.01–1.23). A subsequent analysis, on the basis of ethnicity for the population characteristic, showed that Asians had increased susceptibility to cancer (GG versus AA: OR =1.32, 95% CI: 1.09–1.59; GG + AG versus AA: OR = 1.17, 95% CI: 1.01–1.37). In the subgroup analysis of tumor type, none of the genetic models had statistically significant results. The meta-regression suggested that race and cancer types are not the source of heterogeneity in the present meta-analysis. No publication bias was detected by either the inverted funnel plot or Egger’s test. CONCLUSION: Rs3746444 in miR-499 might be related to susceptibility to cancer.
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spelling pubmed-45501832015-09-04 The association between miR-499 polymorphism and cancer susceptibility: a meta-analysis Xu, Zhongfei Zhang, Enjiao Duan, Weiyi Sun, Changfu Bai, Shuang Tan, Xuexin Onco Targets Ther Original Research BACKGROUND: MicroRNAs are a class of new noncoding RNA that play important roles in the pathogenesis of tumor. Rs3746444 in miR-499 is suggested to be associated with cancer susceptibility. In the present study, we assess the association between miR-499 rs3746444 polymorphism and cancer susceptibility through a meta-analysis. METHODS: We searched relevant articles from the PubMed and Embase databases. We screened all the resulting articles for adherence to the inclusion and exclusion criteria. The associations between miR-499 polymorphism and cancer susceptibility were estimated by computing the odds ratios (ORs) and 95% confidence intervals (CIs). All analyses were performed using Stata software. RESULTS: There are 18 datasets included in the analysis. Statistically significant associations were found between the miR-499 rs3746444 polymorphism and susceptibility to cancer (GG versus AA: OR =1.24, 95% CI: 1.01–1.52; G versus A: OR =1.11, 95% CI: 1.01–1.23). A subsequent analysis, on the basis of ethnicity for the population characteristic, showed that Asians had increased susceptibility to cancer (GG versus AA: OR =1.32, 95% CI: 1.09–1.59; GG + AG versus AA: OR = 1.17, 95% CI: 1.01–1.37). In the subgroup analysis of tumor type, none of the genetic models had statistically significant results. The meta-regression suggested that race and cancer types are not the source of heterogeneity in the present meta-analysis. No publication bias was detected by either the inverted funnel plot or Egger’s test. CONCLUSION: Rs3746444 in miR-499 might be related to susceptibility to cancer. Dove Medical Press 2015-08-20 /pmc/articles/PMC4550183/ /pubmed/26347202 http://dx.doi.org/10.2147/OTT.S88224 Text en © 2015 Xu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Xu, Zhongfei
Zhang, Enjiao
Duan, Weiyi
Sun, Changfu
Bai, Shuang
Tan, Xuexin
The association between miR-499 polymorphism and cancer susceptibility: a meta-analysis
title The association between miR-499 polymorphism and cancer susceptibility: a meta-analysis
title_full The association between miR-499 polymorphism and cancer susceptibility: a meta-analysis
title_fullStr The association between miR-499 polymorphism and cancer susceptibility: a meta-analysis
title_full_unstemmed The association between miR-499 polymorphism and cancer susceptibility: a meta-analysis
title_short The association between miR-499 polymorphism and cancer susceptibility: a meta-analysis
title_sort association between mir-499 polymorphism and cancer susceptibility: a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550183/
https://www.ncbi.nlm.nih.gov/pubmed/26347202
http://dx.doi.org/10.2147/OTT.S88224
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