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Association between TP53 Arg72Pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies
The relationship between the TP53 Arg72Pro polymorphism (rs1042522) and the risk of leukemia remains controversial. Consequently, we performed a meta-analysis to accurately evaluate the association between TP53 Arg72Pro polymorphism and leukemia risk. A comprehensive search was conducted to find all...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823650/ https://www.ncbi.nlm.nih.gov/pubmed/27053289 http://dx.doi.org/10.1038/srep24097 |
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author | Tian, Xin Dai, Shundong Sun, Jing Jiang, Shenyi Jiang, Youhong |
author_facet | Tian, Xin Dai, Shundong Sun, Jing Jiang, Shenyi Jiang, Youhong |
author_sort | Tian, Xin |
collection | PubMed |
description | The relationship between the TP53 Arg72Pro polymorphism (rs1042522) and the risk of leukemia remains controversial. Consequently, we performed a meta-analysis to accurately evaluate the association between TP53 Arg72Pro polymorphism and leukemia risk. A comprehensive search was conducted to find all eligible studies of TP53 Arg72Pro polymorphism and leukemia risk. Fourteen case-control studies, with 2,506 cases and 4,386 controls, were selected for analysis. The overall data failed to indicate a significant association between TP53 Arg72Pro polymorphism and the risk of leukemia (C vs. G: OR = 1.09, 95% CI = 0.93–1.26; CC vs. GC + GG: OR = 1.23, 95% CI = 0.96–1.57). In a subgroup analysis of clinical types, an increased risk was observed in the acute lymphocytic leukemia (ALL) subgroup (CC vs. GC + GG: OR = 1.73; 95% CI = 1.07–2.81) but not in the acute myeloid leukemia (AML) subgroup. In the subgroup analysis, no significant associations with ethnicity and the source of the controls were observed. In conclusion, the results suggest that there is no association between TP53 Arg72Pro polymorphism and the risk of leukemia, but the CC genotype may increase the risk of ALL TP53 Arg72Pro polymorphism CC genotype may increase the risk of ALL but is not associated with AML. Further large-scale, well-designed studies are needed to confirm our results. |
format | Online Article Text |
id | pubmed-4823650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48236502016-04-18 Association between TP53 Arg72Pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies Tian, Xin Dai, Shundong Sun, Jing Jiang, Shenyi Jiang, Youhong Sci Rep Article The relationship between the TP53 Arg72Pro polymorphism (rs1042522) and the risk of leukemia remains controversial. Consequently, we performed a meta-analysis to accurately evaluate the association between TP53 Arg72Pro polymorphism and leukemia risk. A comprehensive search was conducted to find all eligible studies of TP53 Arg72Pro polymorphism and leukemia risk. Fourteen case-control studies, with 2,506 cases and 4,386 controls, were selected for analysis. The overall data failed to indicate a significant association between TP53 Arg72Pro polymorphism and the risk of leukemia (C vs. G: OR = 1.09, 95% CI = 0.93–1.26; CC vs. GC + GG: OR = 1.23, 95% CI = 0.96–1.57). In a subgroup analysis of clinical types, an increased risk was observed in the acute lymphocytic leukemia (ALL) subgroup (CC vs. GC + GG: OR = 1.73; 95% CI = 1.07–2.81) but not in the acute myeloid leukemia (AML) subgroup. In the subgroup analysis, no significant associations with ethnicity and the source of the controls were observed. In conclusion, the results suggest that there is no association between TP53 Arg72Pro polymorphism and the risk of leukemia, but the CC genotype may increase the risk of ALL TP53 Arg72Pro polymorphism CC genotype may increase the risk of ALL but is not associated with AML. Further large-scale, well-designed studies are needed to confirm our results. Nature Publishing Group 2016-04-07 /pmc/articles/PMC4823650/ /pubmed/27053289 http://dx.doi.org/10.1038/srep24097 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Tian, Xin Dai, Shundong Sun, Jing Jiang, Shenyi Jiang, Youhong Association between TP53 Arg72Pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies |
title | Association between TP53 Arg72Pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies |
title_full | Association between TP53 Arg72Pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies |
title_fullStr | Association between TP53 Arg72Pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies |
title_full_unstemmed | Association between TP53 Arg72Pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies |
title_short | Association between TP53 Arg72Pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies |
title_sort | association between tp53 arg72pro polymorphism and leukemia risk: a meta-analysis of 14 case-control studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823650/ https://www.ncbi.nlm.nih.gov/pubmed/27053289 http://dx.doi.org/10.1038/srep24097 |
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