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Association of three micro-RNA gene polymorphisms with the risk of cervical cancer: a meta-analysis and systematic review

OBJECTIVE: Regulation of single nucleotide polymorphisms (SNP) in micro-RNA (miRNA) on the host cells may be one of the most important factors influencing the occurrence of cervical cancer based on the prevalence of HPV infection and the development of cervical cancer. In order to explore the contri...

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Autores principales: Xu, Jingyu, Geng, Junze, Zhang, Qiang, Fan, Yihua, Qi, Zijun, Xia, Tian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675500/
https://www.ncbi.nlm.nih.gov/pubmed/34911543
http://dx.doi.org/10.1186/s12957-021-02463-4
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author Xu, Jingyu
Geng, Junze
Zhang, Qiang
Fan, Yihua
Qi, Zijun
Xia, Tian
author_facet Xu, Jingyu
Geng, Junze
Zhang, Qiang
Fan, Yihua
Qi, Zijun
Xia, Tian
author_sort Xu, Jingyu
collection PubMed
description OBJECTIVE: Regulation of single nucleotide polymorphisms (SNP) in micro-RNA (miRNA) on the host cells may be one of the most important factors influencing the occurrence of cervical cancer based on the prevalence of HPV infection and the development of cervical cancer. In order to explore the contribution of miRNA polymorphism to the occurrence and development of cervical cancer, we conducted an analytical study. METHODS: We selected the polymorphisms of three widely studied miRNAs (miRNA-146a rs2910164, miRNA-499 rs3746444, and miRNA-196a2 rs11614913). Then, we conducted a meta-analysis (for the first time) to investigate their susceptibility to cervical cancer. Case control studies on the correlation between these three miRNAs and cervical cancer susceptibility were investigated by searching on from Pubmed, The Cochrane Library, Embase, CBM, CNKI, Wanfang database, and VIP database. Basic characteristics were recorded and meta-analysis of the case studies was performed using the STATA 15.1 software. RESULTS: The miRNA-146a rs2910164 mutation significantly reduced the risk of cervical cancer in both recessive model (OR = 0.804, 95% CI = 0.652-0.992, P = 0.042; CC vs. CG+GG) and allelic model (OR = 0.845, 95% CI = 0.721-0.991, P = 0.038; C vs. G). There was no significant correlation between miRNA-499 rs3746444 and the risk of cervical cancer. The miRNA-196a2 rs11614913 mutation was significantly associated with a reduced risk of cervical cancer in homozygous model (OR = 0.641, 95% CI = 0.447-0.919, P = 0.016; TT vs. CC), dominant model (OR = 0.795, 95% CI = 0.636-0.994, P = 0.045; CT+TT vs. CC), recessive model (OR = 0.698, 95% CI = 0.532-0.917, P = 0.01; TT vs. CC+CT), and allelic models (OR = 0.783, 95% CI = 0.643-0.954, P = 0.015, T vs. C). CONCLUSION: In summary, this meta-analysis shows that the mutant genotypes of miRNA-146a rs2910164 and miRNA-196a2 rs11614913 are associated with a reduced risk of cervical cancer. Therefore, they may be two gene regulatory points for the prevention of cervical cancer. SYSTEMATIC REVIEW REGISTRATION: PROSPERO registration number CRD42021270079. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12957-021-02463-4.
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spelling pubmed-86755002021-12-20 Association of three micro-RNA gene polymorphisms with the risk of cervical cancer: a meta-analysis and systematic review Xu, Jingyu Geng, Junze Zhang, Qiang Fan, Yihua Qi, Zijun Xia, Tian World J Surg Oncol Research OBJECTIVE: Regulation of single nucleotide polymorphisms (SNP) in micro-RNA (miRNA) on the host cells may be one of the most important factors influencing the occurrence of cervical cancer based on the prevalence of HPV infection and the development of cervical cancer. In order to explore the contribution of miRNA polymorphism to the occurrence and development of cervical cancer, we conducted an analytical study. METHODS: We selected the polymorphisms of three widely studied miRNAs (miRNA-146a rs2910164, miRNA-499 rs3746444, and miRNA-196a2 rs11614913). Then, we conducted a meta-analysis (for the first time) to investigate their susceptibility to cervical cancer. Case control studies on the correlation between these three miRNAs and cervical cancer susceptibility were investigated by searching on from Pubmed, The Cochrane Library, Embase, CBM, CNKI, Wanfang database, and VIP database. Basic characteristics were recorded and meta-analysis of the case studies was performed using the STATA 15.1 software. RESULTS: The miRNA-146a rs2910164 mutation significantly reduced the risk of cervical cancer in both recessive model (OR = 0.804, 95% CI = 0.652-0.992, P = 0.042; CC vs. CG+GG) and allelic model (OR = 0.845, 95% CI = 0.721-0.991, P = 0.038; C vs. G). There was no significant correlation between miRNA-499 rs3746444 and the risk of cervical cancer. The miRNA-196a2 rs11614913 mutation was significantly associated with a reduced risk of cervical cancer in homozygous model (OR = 0.641, 95% CI = 0.447-0.919, P = 0.016; TT vs. CC), dominant model (OR = 0.795, 95% CI = 0.636-0.994, P = 0.045; CT+TT vs. CC), recessive model (OR = 0.698, 95% CI = 0.532-0.917, P = 0.01; TT vs. CC+CT), and allelic models (OR = 0.783, 95% CI = 0.643-0.954, P = 0.015, T vs. C). CONCLUSION: In summary, this meta-analysis shows that the mutant genotypes of miRNA-146a rs2910164 and miRNA-196a2 rs11614913 are associated with a reduced risk of cervical cancer. Therefore, they may be two gene regulatory points for the prevention of cervical cancer. SYSTEMATIC REVIEW REGISTRATION: PROSPERO registration number CRD42021270079. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12957-021-02463-4. BioMed Central 2021-12-16 /pmc/articles/PMC8675500/ /pubmed/34911543 http://dx.doi.org/10.1186/s12957-021-02463-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xu, Jingyu
Geng, Junze
Zhang, Qiang
Fan, Yihua
Qi, Zijun
Xia, Tian
Association of three micro-RNA gene polymorphisms with the risk of cervical cancer: a meta-analysis and systematic review
title Association of three micro-RNA gene polymorphisms with the risk of cervical cancer: a meta-analysis and systematic review
title_full Association of three micro-RNA gene polymorphisms with the risk of cervical cancer: a meta-analysis and systematic review
title_fullStr Association of three micro-RNA gene polymorphisms with the risk of cervical cancer: a meta-analysis and systematic review
title_full_unstemmed Association of three micro-RNA gene polymorphisms with the risk of cervical cancer: a meta-analysis and systematic review
title_short Association of three micro-RNA gene polymorphisms with the risk of cervical cancer: a meta-analysis and systematic review
title_sort association of three micro-rna gene polymorphisms with the risk of cervical cancer: a meta-analysis and systematic review
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675500/
https://www.ncbi.nlm.nih.gov/pubmed/34911543
http://dx.doi.org/10.1186/s12957-021-02463-4
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