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Lack of Association of miR-146a rs2910164 Polymorphism with Gastrointestinal Cancers: Evidence from 10206 Subjects

BACKGROUND: Recent studies on the association between miR-146a rs2910164 polymorphism and risk of gastrointestinal (GI) cancers showed inconclusive results. Accordingly, we conducted a comprehensive literature search and a meta-analysis to clarify the association. METHODOLOGY/PRINCIPAL FINDINGS: Dat...

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Detalles Bibliográficos
Autores principales: Wang, Fang, Sun, Guoping, Zou, Yanfeng, Fan, Lulu, Song, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384592/
https://www.ncbi.nlm.nih.gov/pubmed/22761848
http://dx.doi.org/10.1371/journal.pone.0039623
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author Wang, Fang
Sun, Guoping
Zou, Yanfeng
Fan, Lulu
Song, Bing
author_facet Wang, Fang
Sun, Guoping
Zou, Yanfeng
Fan, Lulu
Song, Bing
author_sort Wang, Fang
collection PubMed
description BACKGROUND: Recent studies on the association between miR-146a rs2910164 polymorphism and risk of gastrointestinal (GI) cancers showed inconclusive results. Accordingly, we conducted a comprehensive literature search and a meta-analysis to clarify the association. METHODOLOGY/PRINCIPAL FINDINGS: Data were collected from the following electronic databases: Pubmed, Excerpta Medica Database (Embase), and Chinese Biomedical Literature Database (CBM), with the last report up to February 24, 2012. The odds ratio (OR) and its 95% confidence interval (95%CI) were used to assess the strength of association. Ultimately, a total of 12 studies (4,817 cases and 5,389 controls) were found to be eligible for meta-analysis. We summarized the data on the association between miR-146a rs2910164 polymorphism and risk of GI cancers in the overall population, and performed subgroup analyses by ethnicity, cancer types, and quality of studies. In the overall analysis, there was no evidence of association between miR-146a rs2910164 polymorphism and the risk of GI cancers (G versus C: OR = 1.07, 95%CI 0.98−1.16, P = 0.14; GG+GC versus CC: OR = 1.14, 95%CI 1.00−1.31, P = 0.05; GG versus GC+CC: OR = 1.06, 95%CI 0.91−1.23, P = 0.47; GG versus CC: OR = 1.17, 95%CI 0.95−1.44, P = 0.13; GC versus CC: OR = 1.14, 95%CI 1.00−1.31, P = 0.05). Similar results were found in the subgroup analyses by ethnicity, cancer types, and quality of studies. CONCLUSIONS/SIGNIFICANCE: This meta-analysis demonstrates that miR-146a rs2910164 polymorphism is not associated with GI cancers susceptibility. More well-designed studies based on larger sample sizes and homogeneous cancer patients are needed.
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spelling pubmed-33845922012-07-03 Lack of Association of miR-146a rs2910164 Polymorphism with Gastrointestinal Cancers: Evidence from 10206 Subjects Wang, Fang Sun, Guoping Zou, Yanfeng Fan, Lulu Song, Bing PLoS One Research Article BACKGROUND: Recent studies on the association between miR-146a rs2910164 polymorphism and risk of gastrointestinal (GI) cancers showed inconclusive results. Accordingly, we conducted a comprehensive literature search and a meta-analysis to clarify the association. METHODOLOGY/PRINCIPAL FINDINGS: Data were collected from the following electronic databases: Pubmed, Excerpta Medica Database (Embase), and Chinese Biomedical Literature Database (CBM), with the last report up to February 24, 2012. The odds ratio (OR) and its 95% confidence interval (95%CI) were used to assess the strength of association. Ultimately, a total of 12 studies (4,817 cases and 5,389 controls) were found to be eligible for meta-analysis. We summarized the data on the association between miR-146a rs2910164 polymorphism and risk of GI cancers in the overall population, and performed subgroup analyses by ethnicity, cancer types, and quality of studies. In the overall analysis, there was no evidence of association between miR-146a rs2910164 polymorphism and the risk of GI cancers (G versus C: OR = 1.07, 95%CI 0.98−1.16, P = 0.14; GG+GC versus CC: OR = 1.14, 95%CI 1.00−1.31, P = 0.05; GG versus GC+CC: OR = 1.06, 95%CI 0.91−1.23, P = 0.47; GG versus CC: OR = 1.17, 95%CI 0.95−1.44, P = 0.13; GC versus CC: OR = 1.14, 95%CI 1.00−1.31, P = 0.05). Similar results were found in the subgroup analyses by ethnicity, cancer types, and quality of studies. CONCLUSIONS/SIGNIFICANCE: This meta-analysis demonstrates that miR-146a rs2910164 polymorphism is not associated with GI cancers susceptibility. More well-designed studies based on larger sample sizes and homogeneous cancer patients are needed. Public Library of Science 2012-06-27 /pmc/articles/PMC3384592/ /pubmed/22761848 http://dx.doi.org/10.1371/journal.pone.0039623 Text en Wang 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
Wang, Fang
Sun, Guoping
Zou, Yanfeng
Fan, Lulu
Song, Bing
Lack of Association of miR-146a rs2910164 Polymorphism with Gastrointestinal Cancers: Evidence from 10206 Subjects
title Lack of Association of miR-146a rs2910164 Polymorphism with Gastrointestinal Cancers: Evidence from 10206 Subjects
title_full Lack of Association of miR-146a rs2910164 Polymorphism with Gastrointestinal Cancers: Evidence from 10206 Subjects
title_fullStr Lack of Association of miR-146a rs2910164 Polymorphism with Gastrointestinal Cancers: Evidence from 10206 Subjects
title_full_unstemmed Lack of Association of miR-146a rs2910164 Polymorphism with Gastrointestinal Cancers: Evidence from 10206 Subjects
title_short Lack of Association of miR-146a rs2910164 Polymorphism with Gastrointestinal Cancers: Evidence from 10206 Subjects
title_sort lack of association of mir-146a rs2910164 polymorphism with gastrointestinal cancers: evidence from 10206 subjects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384592/
https://www.ncbi.nlm.nih.gov/pubmed/22761848
http://dx.doi.org/10.1371/journal.pone.0039623
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