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P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility
BACKGROUND: Tumor suppressor gene p53 plays an important role in the maintenance of the genomic integrity, and mutation in the gene may alter an individual’s susceptibility to various carcinomas. P53 Arg72Pro or codon 72 polymorphism has been indicated to increase the risk of developing certain canc...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484699/ https://www.ncbi.nlm.nih.gov/pubmed/26123760 http://dx.doi.org/10.1186/s12863-015-0235-7 |
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author | Hou, Jun Gu, Ying Hou, Wei Wu, Song Lou, Yin Yang, Wenyu Zhu, Ling Hu, Yukun Sun, Ming Xue, Haowei |
author_facet | Hou, Jun Gu, Ying Hou, Wei Wu, Song Lou, Yin Yang, Wenyu Zhu, Ling Hu, Yukun Sun, Ming Xue, Haowei |
author_sort | Hou, Jun |
collection | PubMed |
description | BACKGROUND: Tumor suppressor gene p53 plays an important role in the maintenance of the genomic integrity, and mutation in the gene may alter an individual’s susceptibility to various carcinomas. P53 Arg72Pro or codon 72 polymorphism has been indicated to increase the risk of developing certain cancers such as bladder cancer and cervical cancer. Human papillomavirus (HPV) infection has been shown as a risk factor for certain cancers such as cervical cancer and oral cancer as well, and the HPV oncoprotein E6 may induce the degradation of p53 function. However, the association between p53 Arg72Pro polymorphism and the risk of oral cancer with HPV infection remains inconclusive. Therefore, this meta-analysis involving 5,614 participants was performed to investigate the relations among the p53 Arg72Pro polymorphism, HPV infection, and the risk of developing oral cancer. RESULTS: A search of the literature by PubMed, Embase, Web of Science, and China National Knowledge Infrastructure databases was conducted to identify studies based on the inclusion and exclusion criteria. Odds ratios with 95 % confidence intervals were combined using a random-effect model or a fixed-effect model. The current study was conducted with 13 studies consisting of 2,413 cases and 3,201 controls. Neither overall analysis nor stratified analyses detected any obvious evidence of association between p53 Arg72Pro polymorphism and oral cancer susceptibility in all genetic models. However, a significant association between p53 Arg72Pro polymorphism and the risk of oral cancer with HPV infection was detected in the Arg/Arg vs. Arg/Pro + Pro/Pro model. CONCLUSION: In the current meta-analysis which used the quantitative data synthesis for the first time, our study demonstrated that p53 Arg72Pro polymorphism together with HPV infection might jointly alter an individual’s susceptibility to the risk of oral cancer. Our results suggested that p53 Arg72Pro polymorphism may partly contribute to the pathogenesis of oral cancer development. |
format | Online Article Text |
id | pubmed-4484699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44846992015-06-30 P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility Hou, Jun Gu, Ying Hou, Wei Wu, Song Lou, Yin Yang, Wenyu Zhu, Ling Hu, Yukun Sun, Ming Xue, Haowei BMC Genet Research Article BACKGROUND: Tumor suppressor gene p53 plays an important role in the maintenance of the genomic integrity, and mutation in the gene may alter an individual’s susceptibility to various carcinomas. P53 Arg72Pro or codon 72 polymorphism has been indicated to increase the risk of developing certain cancers such as bladder cancer and cervical cancer. Human papillomavirus (HPV) infection has been shown as a risk factor for certain cancers such as cervical cancer and oral cancer as well, and the HPV oncoprotein E6 may induce the degradation of p53 function. However, the association between p53 Arg72Pro polymorphism and the risk of oral cancer with HPV infection remains inconclusive. Therefore, this meta-analysis involving 5,614 participants was performed to investigate the relations among the p53 Arg72Pro polymorphism, HPV infection, and the risk of developing oral cancer. RESULTS: A search of the literature by PubMed, Embase, Web of Science, and China National Knowledge Infrastructure databases was conducted to identify studies based on the inclusion and exclusion criteria. Odds ratios with 95 % confidence intervals were combined using a random-effect model or a fixed-effect model. The current study was conducted with 13 studies consisting of 2,413 cases and 3,201 controls. Neither overall analysis nor stratified analyses detected any obvious evidence of association between p53 Arg72Pro polymorphism and oral cancer susceptibility in all genetic models. However, a significant association between p53 Arg72Pro polymorphism and the risk of oral cancer with HPV infection was detected in the Arg/Arg vs. Arg/Pro + Pro/Pro model. CONCLUSION: In the current meta-analysis which used the quantitative data synthesis for the first time, our study demonstrated that p53 Arg72Pro polymorphism together with HPV infection might jointly alter an individual’s susceptibility to the risk of oral cancer. Our results suggested that p53 Arg72Pro polymorphism may partly contribute to the pathogenesis of oral cancer development. BioMed Central 2015-06-30 /pmc/articles/PMC4484699/ /pubmed/26123760 http://dx.doi.org/10.1186/s12863-015-0235-7 Text en © Hou et al. 2015 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hou, Jun Gu, Ying Hou, Wei Wu, Song Lou, Yin Yang, Wenyu Zhu, Ling Hu, Yukun Sun, Ming Xue, Haowei P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility |
title | P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility |
title_full | P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility |
title_fullStr | P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility |
title_full_unstemmed | P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility |
title_short | P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility |
title_sort | p53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484699/ https://www.ncbi.nlm.nih.gov/pubmed/26123760 http://dx.doi.org/10.1186/s12863-015-0235-7 |
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