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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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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. |
format | Online Article Text |
id | pubmed-4550183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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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