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Association between promoter methylation of DAPK gene and HNSCC: A meta-analysis
BACKGROUND: The death-associated protein kinase (DAPK) is a tumor suppressor gene, which is a mediator of cell death of INF-γ–induced apoptosis. Aberrant methylation of DAPK promoter has been reported in patients with head and neck squamous cell carcinoma (HNSCC). However, the results of these studi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332095/ https://www.ncbi.nlm.nih.gov/pubmed/28249042 http://dx.doi.org/10.1371/journal.pone.0173194 |
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author | Cai, Fucheng Xiao, Xiyue Niu, Xun Zhong, Yi |
author_facet | Cai, Fucheng Xiao, Xiyue Niu, Xun Zhong, Yi |
author_sort | Cai, Fucheng |
collection | PubMed |
description | BACKGROUND: The death-associated protein kinase (DAPK) is a tumor suppressor gene, which is a mediator of cell death of INF-γ–induced apoptosis. Aberrant methylation of DAPK promoter has been reported in patients with head and neck squamous cell carcinoma (HNSCC). However, the results of these studies are inconsistent. Hence, the present study aimed to evaluate the association between the promoter methylation of DAPK gene and HNSCC. METHODS: Relevant studies were systematically searched in PubMed, Web of Science, Ovid, and Embase. The association between DAPK promoter methylation and HNSCC was assessed by odds ratio (ORs) and 95% confidence intervals (CI). To evaluate the potential sources of heterogeneity, we conducted the meta-regression analysis and subgroup analysis. RESULTS: Eighteen studies were finally included in the meta-analysis. The frequency of DAPK promoter methylation in patients with HNSCC was 4.09-fold higher than the non-cancerous controls (OR = 3.96, 95%CI = 2.26–6.95). A significant association between DAPK promoter methylation and HNSCC was found among the Asian region and the Non-Asia region (Asian region, OR = 4.43, 95% CI = 2.29–8.58; Non-Asia region, OR = 3.39, 95% CI = 1.18–9.78). In the control source, the significant association between DAPK promoter methylation and HNSCC was seen among the autologous group and the heterogeneous group (autologous group, OR = 2.71, 95% CI = 1.49–4.93; heterogeneous group, OR = 9.50, 95% CI = 2.98–30.27). DAPK promoter methylation was significantly correlated with alcohol status (OR = 1.85, 95% CI = 1.07–3.21). CONCLUSION: The results of this meta-analysis suggested that aberrant methylation of DAPK promoter was associated with HNSCC. |
format | Online Article Text |
id | pubmed-5332095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53320952017-03-10 Association between promoter methylation of DAPK gene and HNSCC: A meta-analysis Cai, Fucheng Xiao, Xiyue Niu, Xun Zhong, Yi PLoS One Research Article BACKGROUND: The death-associated protein kinase (DAPK) is a tumor suppressor gene, which is a mediator of cell death of INF-γ–induced apoptosis. Aberrant methylation of DAPK promoter has been reported in patients with head and neck squamous cell carcinoma (HNSCC). However, the results of these studies are inconsistent. Hence, the present study aimed to evaluate the association between the promoter methylation of DAPK gene and HNSCC. METHODS: Relevant studies were systematically searched in PubMed, Web of Science, Ovid, and Embase. The association between DAPK promoter methylation and HNSCC was assessed by odds ratio (ORs) and 95% confidence intervals (CI). To evaluate the potential sources of heterogeneity, we conducted the meta-regression analysis and subgroup analysis. RESULTS: Eighteen studies were finally included in the meta-analysis. The frequency of DAPK promoter methylation in patients with HNSCC was 4.09-fold higher than the non-cancerous controls (OR = 3.96, 95%CI = 2.26–6.95). A significant association between DAPK promoter methylation and HNSCC was found among the Asian region and the Non-Asia region (Asian region, OR = 4.43, 95% CI = 2.29–8.58; Non-Asia region, OR = 3.39, 95% CI = 1.18–9.78). In the control source, the significant association between DAPK promoter methylation and HNSCC was seen among the autologous group and the heterogeneous group (autologous group, OR = 2.71, 95% CI = 1.49–4.93; heterogeneous group, OR = 9.50, 95% CI = 2.98–30.27). DAPK promoter methylation was significantly correlated with alcohol status (OR = 1.85, 95% CI = 1.07–3.21). CONCLUSION: The results of this meta-analysis suggested that aberrant methylation of DAPK promoter was associated with HNSCC. Public Library of Science 2017-03-01 /pmc/articles/PMC5332095/ /pubmed/28249042 http://dx.doi.org/10.1371/journal.pone.0173194 Text en © 2017 Cai et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Cai, Fucheng Xiao, Xiyue Niu, Xun Zhong, Yi Association between promoter methylation of DAPK gene and HNSCC: A meta-analysis |
title | Association between promoter methylation of DAPK gene and HNSCC: A meta-analysis |
title_full | Association between promoter methylation of DAPK gene and HNSCC: A meta-analysis |
title_fullStr | Association between promoter methylation of DAPK gene and HNSCC: A meta-analysis |
title_full_unstemmed | Association between promoter methylation of DAPK gene and HNSCC: A meta-analysis |
title_short | Association between promoter methylation of DAPK gene and HNSCC: A meta-analysis |
title_sort | association between promoter methylation of dapk gene and hnscc: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332095/ https://www.ncbi.nlm.nih.gov/pubmed/28249042 http://dx.doi.org/10.1371/journal.pone.0173194 |
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