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No Association Between MicroRNA-608 rs4919510 G>C Polymorphism and Digestive System Cancers Susceptibility: A Meta-Analysis Based on 10,836 Individuals

Previous epidemiologic studies have revealed a possible association between microRNA-608 rs4919510 G>C polymorphism and digestive system cancers (DSCs) risk, but the results were not consistent. We therefore performed an updated meta-analysis to explore the association between microRNA-608 rs4919...

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Autores principales: Li, Xue-Feng, Song, Ju-Kun, Cai, Jun-Wei, Zeng, Yu-Qin, Li, Min, Zhu, Jie, Niu, Yu-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999779/
https://www.ncbi.nlm.nih.gov/pubmed/29930517
http://dx.doi.org/10.3389/fphys.2018.00705
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author Li, Xue-Feng
Song, Ju-Kun
Cai, Jun-Wei
Zeng, Yu-Qin
Li, Min
Zhu, Jie
Niu, Yu-Ming
author_facet Li, Xue-Feng
Song, Ju-Kun
Cai, Jun-Wei
Zeng, Yu-Qin
Li, Min
Zhu, Jie
Niu, Yu-Ming
author_sort Li, Xue-Feng
collection PubMed
description Previous epidemiologic studies have revealed a possible association between microRNA-608 rs4919510 G>C polymorphism and digestive system cancers (DSCs) risk, but the results were not consistent. We therefore performed an updated meta-analysis to explore the association between microRNA-608 rs4919510 G>C polymorphism and DSCs risk. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to assess the relationship between the microRNA-608 rs4919510 G>C polymorphism and DSCs risk. Heterogeneity, cumulative analyses, sensitivity analyses, and publication bias were also conducted to examine the statistical power. Eight published articles with nine independent case-control studies involving 10,836 individuals were included in this meta-analysis. Overall, no significant association was found between microRNA-608 rs4919510 G>C polymorphism and DSCs risk in general populations. But some significant protective effects were observed in the subgroup of Caucasian population group in three genetic models (C vs. G: OR = 0.82, 95% CI, 0.68–0.99, P = 0.03, I(2) = 0%; CC vs. GG: OR = 0.59, 95% CI = 0.36–0.97, P = 0.04, I(2) = 0%; GC+CC vs. GG: OR = 0.61, 95% CI = 0.37–0.99, P = 0.05, I(2) = 0%). In summary, current evidence indicates that the microRNA-608 rs4919510 G>C polymorphism maybe an important factor of DSCs susceptibility, especially in Caucasian population.
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spelling pubmed-59997792018-06-21 No Association Between MicroRNA-608 rs4919510 G>C Polymorphism and Digestive System Cancers Susceptibility: A Meta-Analysis Based on 10,836 Individuals Li, Xue-Feng Song, Ju-Kun Cai, Jun-Wei Zeng, Yu-Qin Li, Min Zhu, Jie Niu, Yu-Ming Front Physiol Physiology Previous epidemiologic studies have revealed a possible association between microRNA-608 rs4919510 G>C polymorphism and digestive system cancers (DSCs) risk, but the results were not consistent. We therefore performed an updated meta-analysis to explore the association between microRNA-608 rs4919510 G>C polymorphism and DSCs risk. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to assess the relationship between the microRNA-608 rs4919510 G>C polymorphism and DSCs risk. Heterogeneity, cumulative analyses, sensitivity analyses, and publication bias were also conducted to examine the statistical power. Eight published articles with nine independent case-control studies involving 10,836 individuals were included in this meta-analysis. Overall, no significant association was found between microRNA-608 rs4919510 G>C polymorphism and DSCs risk in general populations. But some significant protective effects were observed in the subgroup of Caucasian population group in three genetic models (C vs. G: OR = 0.82, 95% CI, 0.68–0.99, P = 0.03, I(2) = 0%; CC vs. GG: OR = 0.59, 95% CI = 0.36–0.97, P = 0.04, I(2) = 0%; GC+CC vs. GG: OR = 0.61, 95% CI = 0.37–0.99, P = 0.05, I(2) = 0%). In summary, current evidence indicates that the microRNA-608 rs4919510 G>C polymorphism maybe an important factor of DSCs susceptibility, especially in Caucasian population. Frontiers Media S.A. 2018-06-07 /pmc/articles/PMC5999779/ /pubmed/29930517 http://dx.doi.org/10.3389/fphys.2018.00705 Text en Copyright © 2018 Li, Song, Cai, Zeng, Li, Zhu and Niu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Li, Xue-Feng
Song, Ju-Kun
Cai, Jun-Wei
Zeng, Yu-Qin
Li, Min
Zhu, Jie
Niu, Yu-Ming
No Association Between MicroRNA-608 rs4919510 G>C Polymorphism and Digestive System Cancers Susceptibility: A Meta-Analysis Based on 10,836 Individuals
title No Association Between MicroRNA-608 rs4919510 G>C Polymorphism and Digestive System Cancers Susceptibility: A Meta-Analysis Based on 10,836 Individuals
title_full No Association Between MicroRNA-608 rs4919510 G>C Polymorphism and Digestive System Cancers Susceptibility: A Meta-Analysis Based on 10,836 Individuals
title_fullStr No Association Between MicroRNA-608 rs4919510 G>C Polymorphism and Digestive System Cancers Susceptibility: A Meta-Analysis Based on 10,836 Individuals
title_full_unstemmed No Association Between MicroRNA-608 rs4919510 G>C Polymorphism and Digestive System Cancers Susceptibility: A Meta-Analysis Based on 10,836 Individuals
title_short No Association Between MicroRNA-608 rs4919510 G>C Polymorphism and Digestive System Cancers Susceptibility: A Meta-Analysis Based on 10,836 Individuals
title_sort no association between microrna-608 rs4919510 g>c polymorphism and digestive system cancers susceptibility: a meta-analysis based on 10,836 individuals
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999779/
https://www.ncbi.nlm.nih.gov/pubmed/29930517
http://dx.doi.org/10.3389/fphys.2018.00705
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