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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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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. |
format | Online Article Text |
id | pubmed-4383544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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