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Association between HIC1 promoter methylation and solid tumor: A meta-analysis

The epigenetic silencing of tumor suppressor genes by promoter methylation plays an increasingly important role in cancer research. A number of studies have reported the contribution of HIC1 promoter methylation towards the occurrence and development of solid tumors, even though HIC1 promoter methyl...

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Autores principales: Zhao, Tie, Afrifa, Justice, Wang, Dong, Yu, Jingcui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214777/
https://www.ncbi.nlm.nih.gov/pubmed/32398971
http://dx.doi.org/10.17179/excli2020-1102
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author Zhao, Tie
Afrifa, Justice
Wang, Dong
Yu, Jingcui
author_facet Zhao, Tie
Afrifa, Justice
Wang, Dong
Yu, Jingcui
author_sort Zhao, Tie
collection PubMed
description The epigenetic silencing of tumor suppressor genes by promoter methylation plays an increasingly important role in cancer research. A number of studies have reported the contribution of HIC1 promoter methylation towards the occurrence and development of solid tumors, even though HIC1 promoter methylation has also been found in normal and benign tissue samples. We sought to perform a more accurate and comprehensive meta-analysis to assess the association between HIC1 promoter methylation and cancer risk. We searched and retrieved all published studies on HIC1 promoter methylation in PubMed, Google Scholar, Embase, Cochrane Library, and Web of Science databases. After two reviewers checked the studies and extracted the necessary data independently, the meta-analysis was performed using STATA 12.0 software. A total of 14 case-control studies (949 cancer patients, 282 benign, and 371 normal controls) were included in our study. We report a significantly elevated HIC1 promoter methylation in tumor samples compared to normal (OR = 7.02, 95 % CI 3.12-15.78, P < 0.001) and benign controls (OR = 2.69, 95 % CI 1.13-6.42, P = 0.025). Subgroup analysis stratified by ethnicity showed a significantly reduced heterogeneity among North American (I(2) = 0.0 %, P = 0.502) and European (I(2) = 33.7 %, P = 0.183) samples. In addition, heterogeneity was significantly reduced among MSP based detection method (I(2) = 36.4 %, P = 0.139) when samples were stratified based on the methylation detection methods. The overall outcome demonstrated that HIC1 promoter methylation may be involved in the occurrence and development of solid tumors and has the potential to serve as an epigenetic maker in various specific tumors.
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spelling pubmed-72147772020-05-12 Association between HIC1 promoter methylation and solid tumor: A meta-analysis Zhao, Tie Afrifa, Justice Wang, Dong Yu, Jingcui EXCLI J Original Article The epigenetic silencing of tumor suppressor genes by promoter methylation plays an increasingly important role in cancer research. A number of studies have reported the contribution of HIC1 promoter methylation towards the occurrence and development of solid tumors, even though HIC1 promoter methylation has also been found in normal and benign tissue samples. We sought to perform a more accurate and comprehensive meta-analysis to assess the association between HIC1 promoter methylation and cancer risk. We searched and retrieved all published studies on HIC1 promoter methylation in PubMed, Google Scholar, Embase, Cochrane Library, and Web of Science databases. After two reviewers checked the studies and extracted the necessary data independently, the meta-analysis was performed using STATA 12.0 software. A total of 14 case-control studies (949 cancer patients, 282 benign, and 371 normal controls) were included in our study. We report a significantly elevated HIC1 promoter methylation in tumor samples compared to normal (OR = 7.02, 95 % CI 3.12-15.78, P < 0.001) and benign controls (OR = 2.69, 95 % CI 1.13-6.42, P = 0.025). Subgroup analysis stratified by ethnicity showed a significantly reduced heterogeneity among North American (I(2) = 0.0 %, P = 0.502) and European (I(2) = 33.7 %, P = 0.183) samples. In addition, heterogeneity was significantly reduced among MSP based detection method (I(2) = 36.4 %, P = 0.139) when samples were stratified based on the methylation detection methods. The overall outcome demonstrated that HIC1 promoter methylation may be involved in the occurrence and development of solid tumors and has the potential to serve as an epigenetic maker in various specific tumors. Leibniz Research Centre for Working Environment and Human Factors 2020-04-07 /pmc/articles/PMC7214777/ /pubmed/32398971 http://dx.doi.org/10.17179/excli2020-1102 Text en Copyright © 2020 Zhao et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Zhao, Tie
Afrifa, Justice
Wang, Dong
Yu, Jingcui
Association between HIC1 promoter methylation and solid tumor: A meta-analysis
title Association between HIC1 promoter methylation and solid tumor: A meta-analysis
title_full Association between HIC1 promoter methylation and solid tumor: A meta-analysis
title_fullStr Association between HIC1 promoter methylation and solid tumor: A meta-analysis
title_full_unstemmed Association between HIC1 promoter methylation and solid tumor: A meta-analysis
title_short Association between HIC1 promoter methylation and solid tumor: A meta-analysis
title_sort association between hic1 promoter methylation and solid tumor: a meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214777/
https://www.ncbi.nlm.nih.gov/pubmed/32398971
http://dx.doi.org/10.17179/excli2020-1102
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