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Association between P16(INK4a) Promoter Methylation and HNSCC: A Meta-Analysis of 21 Published Studies

BACKGROUND: The p16(INK4a) is an important tumor suppressor gene (TSG) and aberrant methylation of promoter is known to be a major inactivation mechanism of the tumor suppressor and tumor-related genes. Aberrant TSG methylation was considered an important epigenetic silencing mechanism in the progre...

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Autores principales: Shi, Hao, Chen, Xiong, Lu, Cheng, Gu, Changmei, Jiang, Hongwei, Meng, RuiWei, Niu, Xun, Huang, Yangxin, Lu, Meixia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383544/
https://www.ncbi.nlm.nih.gov/pubmed/25835498
http://dx.doi.org/10.1371/journal.pone.0122302
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author Shi, Hao
Chen, Xiong
Lu, Cheng
Gu, Changmei
Jiang, Hongwei
Meng, RuiWei
Niu, Xun
Huang, Yangxin
Lu, Meixia
author_facet Shi, Hao
Chen, Xiong
Lu, Cheng
Gu, Changmei
Jiang, Hongwei
Meng, RuiWei
Niu, Xun
Huang, Yangxin
Lu, Meixia
author_sort Shi, Hao
collection PubMed
description BACKGROUND: The p16(INK4a) is an important tumor suppressor gene (TSG) and aberrant methylation of promoter is known to be a major inactivation mechanism of the tumor suppressor and tumor-related genes. Aberrant TSG methylation was considered an important epigenetic silencing mechanism in the progression of head and neck squamous cell carcinoma (HNSCC). However, some studies have reported differences in the methylation frequencies of P(16INK4a) promoter between cancer and the corresponding control group. Therefore, we conducted a meta-analysis to better identify the association. METHODS: PubMed, Ovid, ISI Web of Science, and EMBASE were searched to identify eligible studies to evaluate the association of p16(INK4a) promoter methylation and HNSCC. Odds ratio (ORs) and 95% confidence intervals (95%CI) were calculated to evaluate the strength of association between p16(INK4a) promoter methylation and HNSCC. RESULTS: A total of twenty-one studies with 1155 cases and 1017 controls were included in the meta-analysis. The frequencies of p16(INK4a) promoter methylation in the cancer group were significantly higher than those in the control group (cancer group: median: 46.67%, range = 7.84%-95.12%; control group: median: 18.37%, range = 0–83.33%; respectively). The pooled odds ratio was 3.37 (95%CI = 2.32–4.90) in the cancer group versus the corresponding control group under the random-effects model. CONCLUSION: This meta-analysis of 21 published studies identified that aberrant methylation of p16(INK4a) promoter was found to be significantly associated with HNSCC.
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spelling pubmed-43835442015-04-09 Association between P16(INK4a) Promoter Methylation and HNSCC: A Meta-Analysis of 21 Published Studies Shi, Hao Chen, Xiong Lu, Cheng Gu, Changmei Jiang, Hongwei Meng, RuiWei Niu, Xun Huang, Yangxin Lu, Meixia PLoS One Research Article BACKGROUND: The p16(INK4a) is an important tumor suppressor gene (TSG) and aberrant methylation of promoter is known to be a major inactivation mechanism of the tumor suppressor and tumor-related genes. Aberrant TSG methylation was considered an important epigenetic silencing mechanism in the progression of head and neck squamous cell carcinoma (HNSCC). However, some studies have reported differences in the methylation frequencies of P(16INK4a) promoter between cancer and the corresponding control group. Therefore, we conducted a meta-analysis to better identify the association. METHODS: PubMed, Ovid, ISI Web of Science, and EMBASE were searched to identify eligible studies to evaluate the association of p16(INK4a) promoter methylation and HNSCC. Odds ratio (ORs) and 95% confidence intervals (95%CI) were calculated to evaluate the strength of association between p16(INK4a) promoter methylation and HNSCC. RESULTS: A total of twenty-one studies with 1155 cases and 1017 controls were included in the meta-analysis. The frequencies of p16(INK4a) promoter methylation in the cancer group were significantly higher than those in the control group (cancer group: median: 46.67%, range = 7.84%-95.12%; control group: median: 18.37%, range = 0–83.33%; respectively). The pooled odds ratio was 3.37 (95%CI = 2.32–4.90) in the cancer group versus the corresponding control group under the random-effects model. CONCLUSION: This meta-analysis of 21 published studies identified that aberrant methylation of p16(INK4a) promoter was found to be significantly associated with HNSCC. Public Library of Science 2015-04-02 /pmc/articles/PMC4383544/ /pubmed/25835498 http://dx.doi.org/10.1371/journal.pone.0122302 Text en © 2015 Shi 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shi, Hao
Chen, Xiong
Lu, Cheng
Gu, Changmei
Jiang, Hongwei
Meng, RuiWei
Niu, Xun
Huang, Yangxin
Lu, Meixia
Association between P16(INK4a) Promoter Methylation and HNSCC: A Meta-Analysis of 21 Published Studies
title Association between P16(INK4a) Promoter Methylation and HNSCC: A Meta-Analysis of 21 Published Studies
title_full Association between P16(INK4a) Promoter Methylation and HNSCC: A Meta-Analysis of 21 Published Studies
title_fullStr Association between P16(INK4a) Promoter Methylation and HNSCC: A Meta-Analysis of 21 Published Studies
title_full_unstemmed Association between P16(INK4a) Promoter Methylation and HNSCC: A Meta-Analysis of 21 Published Studies
title_short Association between P16(INK4a) Promoter Methylation and HNSCC: A Meta-Analysis of 21 Published Studies
title_sort association between p16(ink4a) promoter methylation and hnscc: a meta-analysis of 21 published studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383544/
https://www.ncbi.nlm.nih.gov/pubmed/25835498
http://dx.doi.org/10.1371/journal.pone.0122302
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