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Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population

Background: miR-146a has been demonstrated to be involved in normal hematopoiesis and the pathogenesis of many hematological malignancies by inhibiting the expression of its targets. Rs2910164(G>C) may modify the expression of the miR-146a gene, which might influence an individual's predispo...

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Autores principales: Zou, Dehua, Yin, Jingwen, Ye, Zhonglv, Zeng, Qiaoli, Tian, Chuan, Wang, Yajun, Chen, Qikang, Chen, Riling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567015/
https://www.ncbi.nlm.nih.gov/pubmed/33133124
http://dx.doi.org/10.3389/fgene.2020.00886
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author Zou, Dehua
Yin, Jingwen
Ye, Zhonglv
Zeng, Qiaoli
Tian, Chuan
Wang, Yajun
Chen, Qikang
Chen, Riling
author_facet Zou, Dehua
Yin, Jingwen
Ye, Zhonglv
Zeng, Qiaoli
Tian, Chuan
Wang, Yajun
Chen, Qikang
Chen, Riling
author_sort Zou, Dehua
collection PubMed
description Background: miR-146a has been demonstrated to be involved in normal hematopoiesis and the pathogenesis of many hematological malignancies by inhibiting the expression of its targets. Rs2910164(G>C) may modify the expression of the miR-146a gene, which might influence an individual's predisposition to childhood acute lymphoblastic leukemia (ALL). However, inconsistent findings have been reported on the association between the rs2910164(G>C) polymorphism and the risk of childhood ALL. Methods: A comprehensive meta-analysis was performed to accurately estimate the association between the miR-146a rs2910164 polymorphism and childhood ALL among four different genetic models. Results: This meta-analysis included Asian studies with a total of 1,543 patients and 1,816 controls. We observed a significant difference between patients and controls for the additive model (CC vs. GG: OR = 1.598, 95% CI: 1.003–2.545, P = 0.049) using a random effects model. Meanwhile, there was a trend of increased childhood ALL risk in the dominant model (CC + CG vs. GG: OR = 1.501, 95% CI: 0.976–2.307, P = 0.065), recessive model (CC vs. GG + CG: OR = 1.142, 95% CI: 0.946–1.380, P = 0.168) and allele model (C vs. G: OR = 1.217, 95% CI: 0.987–1.500, P = 0.066) between patients and controls. Conclusions: Our findings suggest that the miR-146a rs2910164 CC genotype was significantly associated with childhood ALL susceptibility.
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spelling pubmed-75670152020-10-30 Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population Zou, Dehua Yin, Jingwen Ye, Zhonglv Zeng, Qiaoli Tian, Chuan Wang, Yajun Chen, Qikang Chen, Riling Front Genet Genetics Background: miR-146a has been demonstrated to be involved in normal hematopoiesis and the pathogenesis of many hematological malignancies by inhibiting the expression of its targets. Rs2910164(G>C) may modify the expression of the miR-146a gene, which might influence an individual's predisposition to childhood acute lymphoblastic leukemia (ALL). However, inconsistent findings have been reported on the association between the rs2910164(G>C) polymorphism and the risk of childhood ALL. Methods: A comprehensive meta-analysis was performed to accurately estimate the association between the miR-146a rs2910164 polymorphism and childhood ALL among four different genetic models. Results: This meta-analysis included Asian studies with a total of 1,543 patients and 1,816 controls. We observed a significant difference between patients and controls for the additive model (CC vs. GG: OR = 1.598, 95% CI: 1.003–2.545, P = 0.049) using a random effects model. Meanwhile, there was a trend of increased childhood ALL risk in the dominant model (CC + CG vs. GG: OR = 1.501, 95% CI: 0.976–2.307, P = 0.065), recessive model (CC vs. GG + CG: OR = 1.142, 95% CI: 0.946–1.380, P = 0.168) and allele model (C vs. G: OR = 1.217, 95% CI: 0.987–1.500, P = 0.066) between patients and controls. Conclusions: Our findings suggest that the miR-146a rs2910164 CC genotype was significantly associated with childhood ALL susceptibility. Frontiers Media S.A. 2020-10-02 /pmc/articles/PMC7567015/ /pubmed/33133124 http://dx.doi.org/10.3389/fgene.2020.00886 Text en Copyright © 2020 Zou, Yin, Ye, Zeng, Tian, Wang, Chen and Chen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Zou, Dehua
Yin, Jingwen
Ye, Zhonglv
Zeng, Qiaoli
Tian, Chuan
Wang, Yajun
Chen, Qikang
Chen, Riling
Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population
title Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population
title_full Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population
title_fullStr Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population
title_full_unstemmed Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population
title_short Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population
title_sort association between the mir-146a rs2910164 polymorphism and childhood acute lymphoblastic leukemia susceptibility in an asian population
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567015/
https://www.ncbi.nlm.nih.gov/pubmed/33133124
http://dx.doi.org/10.3389/fgene.2020.00886
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