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The association between miR-423 rs6505162 polymorphism and cancer susceptibility: a systematic review and meta-analysis
The association between miR-423 polymorphism (C > A) and the risk of different cancers are still controversial. We performed a meta-analysis to clarify its association with multiple cancer risks. PubMed and Embase (as of 10th September, 2016) were searched. A total of 17 studies from 16 articles,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522323/ https://www.ncbi.nlm.nih.gov/pubmed/28418884 http://dx.doi.org/10.18632/oncotarget.16319 |
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author | Chen, Ru Zheng, Yonglan Zhuo, Lin Wang, Shengfeng |
author_facet | Chen, Ru Zheng, Yonglan Zhuo, Lin Wang, Shengfeng |
author_sort | Chen, Ru |
collection | PubMed |
description | The association between miR-423 polymorphism (C > A) and the risk of different cancers are still controversial. We performed a meta-analysis to clarify its association with multiple cancer risks. PubMed and Embase (as of 10th September, 2016) were searched. A total of 17 studies from 16 articles, consisting of 8,582 cases and 10,291 controls, were finally qualified and enrolled in this meta-analysis. The pooled results showed that the miR-423 AA genotype was associated with decreased cancer risk under the recessive model (odds ratio [OR] = 0.87, 95% confidence interval [CI]: 0.78~0.98, P = 0.020). However, this association became non-significant after excluding the study with the smallest odds ratio. Subgroup analyses revealed a significant decrease in risk of lung cancer (dominant model: OR = 0.73, 95 % CI: 0.60~0.89, P = 0.002; recessive model: OR = 0.59, 95 % CI: 0.37~0.95, P = 0.031). Our study indicates that miR-423 rs6505162 might be associated with a reduced risk of cancers, however, this finding need to be evaluated further in larger samples, especially subgroup analyses. In addition, cancer-specific functional studies are especially needed to reveal the underlying mechanisms between miR-423 and the etiology of cancer. |
format | Online Article Text |
id | pubmed-5522323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55223232017-08-21 The association between miR-423 rs6505162 polymorphism and cancer susceptibility: a systematic review and meta-analysis Chen, Ru Zheng, Yonglan Zhuo, Lin Wang, Shengfeng Oncotarget Research Paper The association between miR-423 polymorphism (C > A) and the risk of different cancers are still controversial. We performed a meta-analysis to clarify its association with multiple cancer risks. PubMed and Embase (as of 10th September, 2016) were searched. A total of 17 studies from 16 articles, consisting of 8,582 cases and 10,291 controls, were finally qualified and enrolled in this meta-analysis. The pooled results showed that the miR-423 AA genotype was associated with decreased cancer risk under the recessive model (odds ratio [OR] = 0.87, 95% confidence interval [CI]: 0.78~0.98, P = 0.020). However, this association became non-significant after excluding the study with the smallest odds ratio. Subgroup analyses revealed a significant decrease in risk of lung cancer (dominant model: OR = 0.73, 95 % CI: 0.60~0.89, P = 0.002; recessive model: OR = 0.59, 95 % CI: 0.37~0.95, P = 0.031). Our study indicates that miR-423 rs6505162 might be associated with a reduced risk of cancers, however, this finding need to be evaluated further in larger samples, especially subgroup analyses. In addition, cancer-specific functional studies are especially needed to reveal the underlying mechanisms between miR-423 and the etiology of cancer. Impact Journals LLC 2017-03-17 /pmc/articles/PMC5522323/ /pubmed/28418884 http://dx.doi.org/10.18632/oncotarget.16319 Text en Copyright: © 2017 Chen et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Chen, Ru Zheng, Yonglan Zhuo, Lin Wang, Shengfeng The association between miR-423 rs6505162 polymorphism and cancer susceptibility: a systematic review and meta-analysis |
title | The association between miR-423 rs6505162 polymorphism and cancer susceptibility: a systematic review and meta-analysis |
title_full | The association between miR-423 rs6505162 polymorphism and cancer susceptibility: a systematic review and meta-analysis |
title_fullStr | The association between miR-423 rs6505162 polymorphism and cancer susceptibility: a systematic review and meta-analysis |
title_full_unstemmed | The association between miR-423 rs6505162 polymorphism and cancer susceptibility: a systematic review and meta-analysis |
title_short | The association between miR-423 rs6505162 polymorphism and cancer susceptibility: a systematic review and meta-analysis |
title_sort | association between mir-423 rs6505162 polymorphism and cancer susceptibility: a systematic review and meta-analysis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522323/ https://www.ncbi.nlm.nih.gov/pubmed/28418884 http://dx.doi.org/10.18632/oncotarget.16319 |
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