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Association between TP53 gene codon72 polymorphism and prostate cancer risk: A systematic review and meta-analysis
BACKGROUND: TP53 gene polymorphism could increase risks of several kinds of cancer. But it remained controversial whether TP53 gene codon72 polymorphism was associated with the susceptibility to prostate cancer. Thus, we conducted a meta-analysis that evaluated the association between TP53 gene codo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636943/ https://www.ncbi.nlm.nih.gov/pubmed/31232967 http://dx.doi.org/10.1097/MD.0000000000016135 |
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author | Han, Pei-Zhen Cao, De-Hong Zhang, Xue-Ling Ren, Zheng-Ju Wei, Qiang |
author_facet | Han, Pei-Zhen Cao, De-Hong Zhang, Xue-Ling Ren, Zheng-Ju Wei, Qiang |
author_sort | Han, Pei-Zhen |
collection | PubMed |
description | BACKGROUND: TP53 gene polymorphism could increase risks of several kinds of cancer. But it remained controversial whether TP53 gene codon72 polymorphism was associated with the susceptibility to prostate cancer. Thus, we conducted a meta-analysis that evaluated the association between TP53 gene codon72 polymorphism and prostate cancer risk. METHOD: A comprehensive research was performed from PubMed, Embase, Web of Science and China National Knowledge Infrastructure (CNKI) up to December 31, 2018. A random effect model was used to evaluate the effect of the outcome. The statistical analyses were performed with Review Manager 5.3.0 and Stata 14.0. The sensitivity analysis and publication bias tests were also performed to confirm the reliability of this meta-analysis. RESULTS: 22 studies included 3146 cases and 4010 controls were involved in this meta-analysis. Overall, no association was observed between TP53 gene codon72 polymorphism and prostate cancer risk (Arg vs Pro: odds ratio [OR] = 1.12, 95% confidence interval [CI] = 0.98–1.30; ArgArg vs ProPro: OR = 1.26, 95% CI = 0.90–1.75; ProPro vs ArgArg+ ArgPro: OR = 1.17, 95% CI = 0.86–1.57; ArgPro+ ProPro vs ArgArg: OR = 1.21, 95% CI = 0.97–1.51). Subgroup analyses, based on ethnicity, source of control and Hardy–Weinberg equilibrium (HWE) status, showed consistent results. CONCLUSION: The meta-analysis we performed showed that there was no association of TP53 gene codon72 polymorphism with prostate cancer risk. |
format | Online Article Text |
id | pubmed-6636943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-66369432019-08-01 Association between TP53 gene codon72 polymorphism and prostate cancer risk: A systematic review and meta-analysis Han, Pei-Zhen Cao, De-Hong Zhang, Xue-Ling Ren, Zheng-Ju Wei, Qiang Medicine (Baltimore) Research Article BACKGROUND: TP53 gene polymorphism could increase risks of several kinds of cancer. But it remained controversial whether TP53 gene codon72 polymorphism was associated with the susceptibility to prostate cancer. Thus, we conducted a meta-analysis that evaluated the association between TP53 gene codon72 polymorphism and prostate cancer risk. METHOD: A comprehensive research was performed from PubMed, Embase, Web of Science and China National Knowledge Infrastructure (CNKI) up to December 31, 2018. A random effect model was used to evaluate the effect of the outcome. The statistical analyses were performed with Review Manager 5.3.0 and Stata 14.0. The sensitivity analysis and publication bias tests were also performed to confirm the reliability of this meta-analysis. RESULTS: 22 studies included 3146 cases and 4010 controls were involved in this meta-analysis. Overall, no association was observed between TP53 gene codon72 polymorphism and prostate cancer risk (Arg vs Pro: odds ratio [OR] = 1.12, 95% confidence interval [CI] = 0.98–1.30; ArgArg vs ProPro: OR = 1.26, 95% CI = 0.90–1.75; ProPro vs ArgArg+ ArgPro: OR = 1.17, 95% CI = 0.86–1.57; ArgPro+ ProPro vs ArgArg: OR = 1.21, 95% CI = 0.97–1.51). Subgroup analyses, based on ethnicity, source of control and Hardy–Weinberg equilibrium (HWE) status, showed consistent results. CONCLUSION: The meta-analysis we performed showed that there was no association of TP53 gene codon72 polymorphism with prostate cancer risk. Wolters Kluwer Health 2019-06-21 /pmc/articles/PMC6636943/ /pubmed/31232967 http://dx.doi.org/10.1097/MD.0000000000016135 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | Research Article Han, Pei-Zhen Cao, De-Hong Zhang, Xue-Ling Ren, Zheng-Ju Wei, Qiang Association between TP53 gene codon72 polymorphism and prostate cancer risk: A systematic review and meta-analysis |
title | Association between TP53 gene codon72 polymorphism and prostate cancer risk: A systematic review and meta-analysis |
title_full | Association between TP53 gene codon72 polymorphism and prostate cancer risk: A systematic review and meta-analysis |
title_fullStr | Association between TP53 gene codon72 polymorphism and prostate cancer risk: A systematic review and meta-analysis |
title_full_unstemmed | Association between TP53 gene codon72 polymorphism and prostate cancer risk: A systematic review and meta-analysis |
title_short | Association between TP53 gene codon72 polymorphism and prostate cancer risk: A systematic review and meta-analysis |
title_sort | association between tp53 gene codon72 polymorphism and prostate cancer risk: a systematic review and meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636943/ https://www.ncbi.nlm.nih.gov/pubmed/31232967 http://dx.doi.org/10.1097/MD.0000000000016135 |
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