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Association of miR-608 rs4919510 polymorphism and cancer risk: a meta-analysis based on 13,664 subjects
Single nucleotide polymorphisms (SNPs) in MicroRNAs (miRNAs) are involved in the mechanism of carcinogenesis. Several studies have evaluated the association of rs4919510 SNP in miR-608 with cancer susceptibility in different types of cancer, with inconclusive outcomes. To obtain a more precise estim...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514889/ https://www.ncbi.nlm.nih.gov/pubmed/27223084 http://dx.doi.org/10.18632/oncotarget.9509 |
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author | Liu, Huiquan Zhou, Yaqun Liu, Qingquan Xiao, Guangqin Wang, Bangyan Li, Weijuan Ye, Dawei Yu, Shiying |
author_facet | Liu, Huiquan Zhou, Yaqun Liu, Qingquan Xiao, Guangqin Wang, Bangyan Li, Weijuan Ye, Dawei Yu, Shiying |
author_sort | Liu, Huiquan |
collection | PubMed |
description | Single nucleotide polymorphisms (SNPs) in MicroRNAs (miRNAs) are involved in the mechanism of carcinogenesis. Several studies have evaluated the association of rs4919510 SNP in miR-608 with cancer susceptibility in different types of cancer, with inconclusive outcomes. To obtain a more precise estimation, we carried out this meta-analysis through systematic retrieval from the PubMed and Embase database. A total of 10 case-control studies were analyzed with 6,000 cases and 7,664 controls. The results showed that 4919510 SNP in miR-608 was significantly associated with decreased cancer risk only in recessive model (CC vs. GG+GC: OR=0.89, 95% CI: 0.82-0.97, P=0.009). By further stratified analysis, we found that rs4919510 SNP had some relationship with decreased cancer risk in both homozygote model (CC vs. GG: OR=0.59, 95% CI: 0.36-0.96, P=0.034) and dominant model (CG+ CC vs. GG: OR=0.60, 95% CI: 0.37-0.98, P=0.042) in Caucasians but no relationship in any genetic model in Asians. These results indicated that miR-608 rs4919510 polymorphism may contribute to the decreased cancer susceptibility and could be a promising target to forecast cancer risk for clinical practice. However, to further confirm these results, well-designed large scale case–control studies are needed in the future. |
format | Online Article Text |
id | pubmed-5514889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55148892017-07-24 Association of miR-608 rs4919510 polymorphism and cancer risk: a meta-analysis based on 13,664 subjects Liu, Huiquan Zhou, Yaqun Liu, Qingquan Xiao, Guangqin Wang, Bangyan Li, Weijuan Ye, Dawei Yu, Shiying Oncotarget Research Paper Single nucleotide polymorphisms (SNPs) in MicroRNAs (miRNAs) are involved in the mechanism of carcinogenesis. Several studies have evaluated the association of rs4919510 SNP in miR-608 with cancer susceptibility in different types of cancer, with inconclusive outcomes. To obtain a more precise estimation, we carried out this meta-analysis through systematic retrieval from the PubMed and Embase database. A total of 10 case-control studies were analyzed with 6,000 cases and 7,664 controls. The results showed that 4919510 SNP in miR-608 was significantly associated with decreased cancer risk only in recessive model (CC vs. GG+GC: OR=0.89, 95% CI: 0.82-0.97, P=0.009). By further stratified analysis, we found that rs4919510 SNP had some relationship with decreased cancer risk in both homozygote model (CC vs. GG: OR=0.59, 95% CI: 0.36-0.96, P=0.034) and dominant model (CG+ CC vs. GG: OR=0.60, 95% CI: 0.37-0.98, P=0.042) in Caucasians but no relationship in any genetic model in Asians. These results indicated that miR-608 rs4919510 polymorphism may contribute to the decreased cancer susceptibility and could be a promising target to forecast cancer risk for clinical practice. However, to further confirm these results, well-designed large scale case–control studies are needed in the future. Impact Journals LLC 2016-05-20 /pmc/articles/PMC5514889/ /pubmed/27223084 http://dx.doi.org/10.18632/oncotarget.9509 Text en Copyright: © 2017 Liu 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 (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Liu, Huiquan Zhou, Yaqun Liu, Qingquan Xiao, Guangqin Wang, Bangyan Li, Weijuan Ye, Dawei Yu, Shiying Association of miR-608 rs4919510 polymorphism and cancer risk: a meta-analysis based on 13,664 subjects |
title | Association of miR-608 rs4919510 polymorphism and cancer risk: a meta-analysis based on 13,664 subjects |
title_full | Association of miR-608 rs4919510 polymorphism and cancer risk: a meta-analysis based on 13,664 subjects |
title_fullStr | Association of miR-608 rs4919510 polymorphism and cancer risk: a meta-analysis based on 13,664 subjects |
title_full_unstemmed | Association of miR-608 rs4919510 polymorphism and cancer risk: a meta-analysis based on 13,664 subjects |
title_short | Association of miR-608 rs4919510 polymorphism and cancer risk: a meta-analysis based on 13,664 subjects |
title_sort | association of mir-608 rs4919510 polymorphism and cancer risk: a meta-analysis based on 13,664 subjects |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514889/ https://www.ncbi.nlm.nih.gov/pubmed/27223084 http://dx.doi.org/10.18632/oncotarget.9509 |
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