Cargando…
The Role of TP53 Gene Codon 72 Polymorphism in Leukemia: A PRISMA-Compliant Systematic Review and Meta-Analysis
The purpose of this meta-analysis was aimed to evaluate the association of tumor protein p53 (TP53) gene codon 72 polymorphism with leukemia susceptibility. We searched PubMed to identify relevant studies, and 16 case-control studies from 14 published articles were identified as eligible studies, in...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635761/ https://www.ncbi.nlm.nih.gov/pubmed/26402821 http://dx.doi.org/10.1097/MD.0000000000001588 |
_version_ | 1782399550085922816 |
---|---|
author | Ruan, Xiao-Lan Li, Sheng Meng, Xiang-Yu Geng, Peiliang Gao, Qing-Ping Ao, Xu-Bin |
author_facet | Ruan, Xiao-Lan Li, Sheng Meng, Xiang-Yu Geng, Peiliang Gao, Qing-Ping Ao, Xu-Bin |
author_sort | Ruan, Xiao-Lan |
collection | PubMed |
description | The purpose of this meta-analysis was aimed to evaluate the association of tumor protein p53 (TP53) gene codon 72 polymorphism with leukemia susceptibility. We searched PubMed to identify relevant studies, and 16 case-control studies from 14 published articles were identified as eligible studies, including 2062 leukemia patients and 5826 controls. After extracting data, odds ratio (OR) with the corresponding 95% confidence interval (95%CI) was applied to assess the association between TP53 codon 72 polymorphism and leukemia susceptibility. The meta-analysis was performed with the Comprehensive Meta-Analysis software, version 2.2. Overall, no significant association between TP53 codon 72 polymorphism and leukemia susceptibility was found in this meta-analysis (Pro vs Arg: OR = 1.05, 95%CI = 0.90–1.21; Pro/Pro vs Arg/Arg: OR = 1.13, 95%CI = 0.84–1.52; Arg/Pro vs Arg/Arg: OR = 0.94, 95%CI = 0.76–1.15; [Pro/Pro + Arg/Pro] vs Arg/Arg: OR = 0.99, 95%CI = 0.80–1.21; Pro/Pro vs [Arg/Arg + Arg/Pro]: OR = 1.19, 95%CI = 0.93–1.51). Similar results were also found in subgroup analysis by ethnicity, source of controls, and types of leukemia (either acute myeloid leukemia or acute lymphocytic leukemia). Our meta-analysis demonstrates that TP53 codon 72 polymorphism may not be a risk factor for acute leukemia; however, due to the limitations of this study, it should be verified in future studies. |
format | Online Article Text |
id | pubmed-4635761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-46357612015-12-16 The Role of TP53 Gene Codon 72 Polymorphism in Leukemia: A PRISMA-Compliant Systematic Review and Meta-Analysis Ruan, Xiao-Lan Li, Sheng Meng, Xiang-Yu Geng, Peiliang Gao, Qing-Ping Ao, Xu-Bin Medicine (Baltimore) 4800 The purpose of this meta-analysis was aimed to evaluate the association of tumor protein p53 (TP53) gene codon 72 polymorphism with leukemia susceptibility. We searched PubMed to identify relevant studies, and 16 case-control studies from 14 published articles were identified as eligible studies, including 2062 leukemia patients and 5826 controls. After extracting data, odds ratio (OR) with the corresponding 95% confidence interval (95%CI) was applied to assess the association between TP53 codon 72 polymorphism and leukemia susceptibility. The meta-analysis was performed with the Comprehensive Meta-Analysis software, version 2.2. Overall, no significant association between TP53 codon 72 polymorphism and leukemia susceptibility was found in this meta-analysis (Pro vs Arg: OR = 1.05, 95%CI = 0.90–1.21; Pro/Pro vs Arg/Arg: OR = 1.13, 95%CI = 0.84–1.52; Arg/Pro vs Arg/Arg: OR = 0.94, 95%CI = 0.76–1.15; [Pro/Pro + Arg/Pro] vs Arg/Arg: OR = 0.99, 95%CI = 0.80–1.21; Pro/Pro vs [Arg/Arg + Arg/Pro]: OR = 1.19, 95%CI = 0.93–1.51). Similar results were also found in subgroup analysis by ethnicity, source of controls, and types of leukemia (either acute myeloid leukemia or acute lymphocytic leukemia). Our meta-analysis demonstrates that TP53 codon 72 polymorphism may not be a risk factor for acute leukemia; however, due to the limitations of this study, it should be verified in future studies. Wolters Kluwer Health 2015-09-25 /pmc/articles/PMC4635761/ /pubmed/26402821 http://dx.doi.org/10.1097/MD.0000000000001588 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-nc-sa/4.0 |
spellingShingle | 4800 Ruan, Xiao-Lan Li, Sheng Meng, Xiang-Yu Geng, Peiliang Gao, Qing-Ping Ao, Xu-Bin The Role of TP53 Gene Codon 72 Polymorphism in Leukemia: A PRISMA-Compliant Systematic Review and Meta-Analysis |
title | The Role of TP53 Gene Codon 72 Polymorphism in Leukemia: A PRISMA-Compliant Systematic Review and Meta-Analysis |
title_full | The Role of TP53 Gene Codon 72 Polymorphism in Leukemia: A PRISMA-Compliant Systematic Review and Meta-Analysis |
title_fullStr | The Role of TP53 Gene Codon 72 Polymorphism in Leukemia: A PRISMA-Compliant Systematic Review and Meta-Analysis |
title_full_unstemmed | The Role of TP53 Gene Codon 72 Polymorphism in Leukemia: A PRISMA-Compliant Systematic Review and Meta-Analysis |
title_short | The Role of TP53 Gene Codon 72 Polymorphism in Leukemia: A PRISMA-Compliant Systematic Review and Meta-Analysis |
title_sort | role of tp53 gene codon 72 polymorphism in leukemia: a prisma-compliant systematic review and meta-analysis |
topic | 4800 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635761/ https://www.ncbi.nlm.nih.gov/pubmed/26402821 http://dx.doi.org/10.1097/MD.0000000000001588 |
work_keys_str_mv | AT ruanxiaolan theroleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT lisheng theroleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT mengxiangyu theroleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT gengpeiliang theroleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT gaoqingping theroleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT aoxubin theroleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT ruanxiaolan roleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT lisheng roleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT mengxiangyu roleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT gengpeiliang roleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT gaoqingping roleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis AT aoxubin roleoftp53genecodon72polymorphisminleukemiaaprismacompliantsystematicreviewandmetaanalysis |