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Association between eight hypermethylation-related genes and gastric cancer: a systematic review and meta-analysis

BACKGROUND: Although multiple gene promoter hypermethylation has been associated with gastric carcinogenesis, data on their specific relationship remains scant. We aimed to investigate the correlation between the status of multiple gene promoter methylation and gastric cancer (GC). METHODS: We searc...

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Autores principales: Ma, Chenhui, Wang, Bofang, Pu, Weigao, Ma, Huanhuan, Song, Kewei, Wang, Na, Deng, Xiaobo, Chen, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372225/
https://www.ncbi.nlm.nih.gov/pubmed/35966315
http://dx.doi.org/10.21037/tcr-22-372
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author Ma, Chenhui
Wang, Bofang
Pu, Weigao
Ma, Huanhuan
Song, Kewei
Wang, Na
Deng, Xiaobo
Chen, Hao
author_facet Ma, Chenhui
Wang, Bofang
Pu, Weigao
Ma, Huanhuan
Song, Kewei
Wang, Na
Deng, Xiaobo
Chen, Hao
author_sort Ma, Chenhui
collection PubMed
description BACKGROUND: Although multiple gene promoter hypermethylation has been associated with gastric carcinogenesis, data on their specific relationship remains scant. We aimed to investigate the correlation between the status of multiple gene promoter methylation and gastric cancer (GC). METHODS: We searched PubMed, EMBASE, CNKI, Wanfang, Cqvip and Cochrane Library up to May 2021. We systematically assessed the association between methylation status of the CpG islands and the risk of GC. We compared the incidence of DNA methylation between tumor and non-tumor tissues, and evaluated the clinicopathological significance of the DNA methylation in gastric carcinoma. The data was presented by an odds ratio (OR) with an accompanying 95% confidence interval (CI). We then generated forest plots calculated by fixed-effects or random-effects model. RESULTS: This study enrolled a total of 201 studies (140 papers). Our analysis showed a higher frequency of methylation of the CpG islands in GC tissues compared to non-neoplastic tissues. Besides, the data demonstrated that polygene’s aberrant promoter methylation might be linked to the initial development and progression of GC. DISCUSSION: The genes with altered DNA methylation might serve as epigenetic biomarkers, providing a promising molecular diagnostic and prognostic tool for human GC. However, our findings need further evaluation in large randomized controlled trials.
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spelling pubmed-93722252022-08-13 Association between eight hypermethylation-related genes and gastric cancer: a systematic review and meta-analysis Ma, Chenhui Wang, Bofang Pu, Weigao Ma, Huanhuan Song, Kewei Wang, Na Deng, Xiaobo Chen, Hao Transl Cancer Res Original Article BACKGROUND: Although multiple gene promoter hypermethylation has been associated with gastric carcinogenesis, data on their specific relationship remains scant. We aimed to investigate the correlation between the status of multiple gene promoter methylation and gastric cancer (GC). METHODS: We searched PubMed, EMBASE, CNKI, Wanfang, Cqvip and Cochrane Library up to May 2021. We systematically assessed the association between methylation status of the CpG islands and the risk of GC. We compared the incidence of DNA methylation between tumor and non-tumor tissues, and evaluated the clinicopathological significance of the DNA methylation in gastric carcinoma. The data was presented by an odds ratio (OR) with an accompanying 95% confidence interval (CI). We then generated forest plots calculated by fixed-effects or random-effects model. RESULTS: This study enrolled a total of 201 studies (140 papers). Our analysis showed a higher frequency of methylation of the CpG islands in GC tissues compared to non-neoplastic tissues. Besides, the data demonstrated that polygene’s aberrant promoter methylation might be linked to the initial development and progression of GC. DISCUSSION: The genes with altered DNA methylation might serve as epigenetic biomarkers, providing a promising molecular diagnostic and prognostic tool for human GC. However, our findings need further evaluation in large randomized controlled trials. AME Publishing Company 2022-07 /pmc/articles/PMC9372225/ /pubmed/35966315 http://dx.doi.org/10.21037/tcr-22-372 Text en 2022 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Ma, Chenhui
Wang, Bofang
Pu, Weigao
Ma, Huanhuan
Song, Kewei
Wang, Na
Deng, Xiaobo
Chen, Hao
Association between eight hypermethylation-related genes and gastric cancer: a systematic review and meta-analysis
title Association between eight hypermethylation-related genes and gastric cancer: a systematic review and meta-analysis
title_full Association between eight hypermethylation-related genes and gastric cancer: a systematic review and meta-analysis
title_fullStr Association between eight hypermethylation-related genes and gastric cancer: a systematic review and meta-analysis
title_full_unstemmed Association between eight hypermethylation-related genes and gastric cancer: a systematic review and meta-analysis
title_short Association between eight hypermethylation-related genes and gastric cancer: a systematic review and meta-analysis
title_sort association between eight hypermethylation-related genes and gastric cancer: a systematic review and meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372225/
https://www.ncbi.nlm.nih.gov/pubmed/35966315
http://dx.doi.org/10.21037/tcr-22-372
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