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rs11614913 polymorphism in miRNA-196a2 and cancer risk: an updated meta-analysis

Several epidemiological studies have reported that polymorphisms in microRNA-196a2 (miR-196a2) were associated with various cancers. However, the results remained unverified and were inconsistent in different cancers. Therefore, we carried out an updated meta-analysis to elaborate the effects of rs1...

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Autores principales: Liu, Yuhan, He, Anbang, Liu, Baoer, Zhong, Yucheng, Liao, Xinhui, Yang, Jiangeng, Chen, Jieqing, Wu, Jianting, Mei, Hongbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840307/
https://www.ncbi.nlm.nih.gov/pubmed/29535537
http://dx.doi.org/10.2147/OTT.S154211
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author Liu, Yuhan
He, Anbang
Liu, Baoer
Zhong, Yucheng
Liao, Xinhui
Yang, Jiangeng
Chen, Jieqing
Wu, Jianting
Mei, Hongbing
author_facet Liu, Yuhan
He, Anbang
Liu, Baoer
Zhong, Yucheng
Liao, Xinhui
Yang, Jiangeng
Chen, Jieqing
Wu, Jianting
Mei, Hongbing
author_sort Liu, Yuhan
collection PubMed
description Several epidemiological studies have reported that polymorphisms in microRNA-196a2 (miR-196a2) were associated with various cancers. However, the results remained unverified and were inconsistent in different cancers. Therefore, we carried out an updated meta-analysis to elaborate the effects of rs11614913 polymorphism on cancer susceptibility. A total of 84 articles with 35,802 cases and 41,541 controls were included to evaluate the association between the miR-196a2 rs11614913 and cancer risk by pooled odds ratios (ORs) and 95% confidence intervals (CIs). The results showed that miR-196a2 rs11614913 polymorphism is associated with cancer susceptibility, especially in lung cancer (homozygote comparison, OR =0.840, 95% CI =0.734–0.961; recessive model, OR =0.858, 95% CI =0.771–0.955), hepatocellular carcinoma (allelic contrast, OR =0.894, 95% CI =0.800–0.998; homozygote comparison, OR =0.900, 95% CI =0.813–0.997; recessive model, OR =0.800, 95% CI =0.678–0.944), and head and neck cancer (allelic contrast, OR =1.076, 95% CI =1.006–1.152; homozygote comparison, OR =1.214, 95% CI =1.043–1.413). In addition, significant association was found among Asian populations (allele model, OR =0.847, 95% CI =0.899–0.997, P=0.038; homozygote model, OR =0.878, 95% CI =0.788–0.977, P=0.017; recessive model, OR =0.895, 95% CI =0.824–0.972, P=0.008) but not in Caucasians. The updated meta-analysis confirmed the previous results that miR-196a2 rs11614913 polymorphism may serve as a risk factor for patients with cancers.
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spelling pubmed-58403072018-03-13 rs11614913 polymorphism in miRNA-196a2 and cancer risk: an updated meta-analysis Liu, Yuhan He, Anbang Liu, Baoer Zhong, Yucheng Liao, Xinhui Yang, Jiangeng Chen, Jieqing Wu, Jianting Mei, Hongbing Onco Targets Ther Review Several epidemiological studies have reported that polymorphisms in microRNA-196a2 (miR-196a2) were associated with various cancers. However, the results remained unverified and were inconsistent in different cancers. Therefore, we carried out an updated meta-analysis to elaborate the effects of rs11614913 polymorphism on cancer susceptibility. A total of 84 articles with 35,802 cases and 41,541 controls were included to evaluate the association between the miR-196a2 rs11614913 and cancer risk by pooled odds ratios (ORs) and 95% confidence intervals (CIs). The results showed that miR-196a2 rs11614913 polymorphism is associated with cancer susceptibility, especially in lung cancer (homozygote comparison, OR =0.840, 95% CI =0.734–0.961; recessive model, OR =0.858, 95% CI =0.771–0.955), hepatocellular carcinoma (allelic contrast, OR =0.894, 95% CI =0.800–0.998; homozygote comparison, OR =0.900, 95% CI =0.813–0.997; recessive model, OR =0.800, 95% CI =0.678–0.944), and head and neck cancer (allelic contrast, OR =1.076, 95% CI =1.006–1.152; homozygote comparison, OR =1.214, 95% CI =1.043–1.413). In addition, significant association was found among Asian populations (allele model, OR =0.847, 95% CI =0.899–0.997, P=0.038; homozygote model, OR =0.878, 95% CI =0.788–0.977, P=0.017; recessive model, OR =0.895, 95% CI =0.824–0.972, P=0.008) but not in Caucasians. The updated meta-analysis confirmed the previous results that miR-196a2 rs11614913 polymorphism may serve as a risk factor for patients with cancers. Dove Medical Press 2018-03-01 /pmc/articles/PMC5840307/ /pubmed/29535537 http://dx.doi.org/10.2147/OTT.S154211 Text en © 2018 Liu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Liu, Yuhan
He, Anbang
Liu, Baoer
Zhong, Yucheng
Liao, Xinhui
Yang, Jiangeng
Chen, Jieqing
Wu, Jianting
Mei, Hongbing
rs11614913 polymorphism in miRNA-196a2 and cancer risk: an updated meta-analysis
title rs11614913 polymorphism in miRNA-196a2 and cancer risk: an updated meta-analysis
title_full rs11614913 polymorphism in miRNA-196a2 and cancer risk: an updated meta-analysis
title_fullStr rs11614913 polymorphism in miRNA-196a2 and cancer risk: an updated meta-analysis
title_full_unstemmed rs11614913 polymorphism in miRNA-196a2 and cancer risk: an updated meta-analysis
title_short rs11614913 polymorphism in miRNA-196a2 and cancer risk: an updated meta-analysis
title_sort rs11614913 polymorphism in mirna-196a2 and cancer risk: an updated meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840307/
https://www.ncbi.nlm.nih.gov/pubmed/29535537
http://dx.doi.org/10.2147/OTT.S154211
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