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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Leibniz Research Centre for Working Environment and Human Factors
2020
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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. |
format | Online Article Text |
id | pubmed-7214777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Leibniz Research Centre for Working Environment and Human Factors |
record_format | MEDLINE/PubMed |
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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