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Aberrant Methylation of RASSF1A Closely Associated with HNSCC, a Meta-Analysis

The RAS association domain family protein 1a (RASSF1A), a tumor suppressor gene at 3p21.3, plays a very important role in various cancers, including the head and neck squamous cell carcinoma (HNSCC). Hypermethylation of CpG islands in the RASSF1A promoter region contribute to epigenetic inactivation...

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Autores principales: Meng, Rui-Wei, Li, Yun-Cheng, Chen, Xiong, Huang, Yang-Xin, Shi, Hao, Du, Dan-Dan, Niu, Xun, Lu, Cheng, Lu, Mei-Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746596/
https://www.ncbi.nlm.nih.gov/pubmed/26857374
http://dx.doi.org/10.1038/srep20756
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author Meng, Rui-Wei
Li, Yun-Cheng
Chen, Xiong
Huang, Yang-Xin
Shi, Hao
Du, Dan-Dan
Niu, Xun
Lu, Cheng
Lu, Mei-Xia
author_facet Meng, Rui-Wei
Li, Yun-Cheng
Chen, Xiong
Huang, Yang-Xin
Shi, Hao
Du, Dan-Dan
Niu, Xun
Lu, Cheng
Lu, Mei-Xia
author_sort Meng, Rui-Wei
collection PubMed
description The RAS association domain family protein 1a (RASSF1A), a tumor suppressor gene at 3p21.3, plays a very important role in various cancers, including the head and neck squamous cell carcinoma (HNSCC). Hypermethylation of CpG islands in the RASSF1A promoter region contribute to epigenetic inactivation. However, the association between RASSF1A promoter methylation and HNSCC remains unclear and controversial. Therefore, a meta-analysis was performed in the study to identify the association. We identified the eligible studies through searching PubMed, EMBASE, Web of Science, and China National Knowledge Infrastructure (CNKI) databases with a systematic searching strategy. The information on characteristics of each study and prevalence of RASSF1A methylation were collected. Pooled odds ratios (ORs) with corresponding confidence intervals (CIs) were calculated. Meta-regression was performed to analyze heterogeneity and funnel plots were applied to evaluate publication bias. A total of 550 HNSCC patients and 404 controls from twelve eligible studies were included in the meta-analysis. Overall, a significant association was observed between RASSF1A methylation status and HNSCC risk under a random-effects model (OR = 2.93, 95% CI: 1.58–5.46). There was no significant publication bias observed. The meta-analysis suggested that there was a significant association between aberrant RASSF1A methylation and HNSCC.
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spelling pubmed-47465962016-02-17 Aberrant Methylation of RASSF1A Closely Associated with HNSCC, a Meta-Analysis Meng, Rui-Wei Li, Yun-Cheng Chen, Xiong Huang, Yang-Xin Shi, Hao Du, Dan-Dan Niu, Xun Lu, Cheng Lu, Mei-Xia Sci Rep Article The RAS association domain family protein 1a (RASSF1A), a tumor suppressor gene at 3p21.3, plays a very important role in various cancers, including the head and neck squamous cell carcinoma (HNSCC). Hypermethylation of CpG islands in the RASSF1A promoter region contribute to epigenetic inactivation. However, the association between RASSF1A promoter methylation and HNSCC remains unclear and controversial. Therefore, a meta-analysis was performed in the study to identify the association. We identified the eligible studies through searching PubMed, EMBASE, Web of Science, and China National Knowledge Infrastructure (CNKI) databases with a systematic searching strategy. The information on characteristics of each study and prevalence of RASSF1A methylation were collected. Pooled odds ratios (ORs) with corresponding confidence intervals (CIs) were calculated. Meta-regression was performed to analyze heterogeneity and funnel plots were applied to evaluate publication bias. A total of 550 HNSCC patients and 404 controls from twelve eligible studies were included in the meta-analysis. Overall, a significant association was observed between RASSF1A methylation status and HNSCC risk under a random-effects model (OR = 2.93, 95% CI: 1.58–5.46). There was no significant publication bias observed. The meta-analysis suggested that there was a significant association between aberrant RASSF1A methylation and HNSCC. Nature Publishing Group 2016-02-09 /pmc/articles/PMC4746596/ /pubmed/26857374 http://dx.doi.org/10.1038/srep20756 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Meng, Rui-Wei
Li, Yun-Cheng
Chen, Xiong
Huang, Yang-Xin
Shi, Hao
Du, Dan-Dan
Niu, Xun
Lu, Cheng
Lu, Mei-Xia
Aberrant Methylation of RASSF1A Closely Associated with HNSCC, a Meta-Analysis
title Aberrant Methylation of RASSF1A Closely Associated with HNSCC, a Meta-Analysis
title_full Aberrant Methylation of RASSF1A Closely Associated with HNSCC, a Meta-Analysis
title_fullStr Aberrant Methylation of RASSF1A Closely Associated with HNSCC, a Meta-Analysis
title_full_unstemmed Aberrant Methylation of RASSF1A Closely Associated with HNSCC, a Meta-Analysis
title_short Aberrant Methylation of RASSF1A Closely Associated with HNSCC, a Meta-Analysis
title_sort aberrant methylation of rassf1a closely associated with hnscc, a meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746596/
https://www.ncbi.nlm.nih.gov/pubmed/26857374
http://dx.doi.org/10.1038/srep20756
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