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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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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. |
format | Online Article Text |
id | pubmed-5840307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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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