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Polymorphisms of the CYR61 gene in patients with acute myeloid leukemia in a Han Chinese population

It was demonstrated in previous studies that cysteine-rich angiogenic inducer 61 (Cyr61) plays vital roles in hematological disorders, and we have already reported that the Cyr61 protein is a tumor promoter in acute myeloid leukemia (AML). Here, we investigated the association between CYR61 gene pol...

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Autores principales: Niu, Chang-Chun, Wan, Ya-Fang, Yang, Cheng, Li, Tian, Liao, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112968/
https://www.ncbi.nlm.nih.gov/pubmed/30142822
http://dx.doi.org/10.1097/MD.0000000000011963
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author Niu, Chang-Chun
Wan, Ya-Fang
Yang, Cheng
Li, Tian
Liao, Pu
author_facet Niu, Chang-Chun
Wan, Ya-Fang
Yang, Cheng
Li, Tian
Liao, Pu
author_sort Niu, Chang-Chun
collection PubMed
description It was demonstrated in previous studies that cysteine-rich angiogenic inducer 61 (Cyr61) plays vital roles in hematological disorders, and we have already reported that the Cyr61 protein is a tumor promoter in acute myeloid leukemia (AML). Here, we investigated the association between CYR61 gene polymorphisms and susceptibility to AML. We genotyped 2 single-nucleotide polymorphisms (rs2297141 and rs6576776) in the region of the CYR61 gene by improved multiplex ligase detection reaction genotyping assays in a total of 275 samples, including samples from 137 AML patients and 138 healthy controls. Chi-squared tests and logistic regression analysis were performed to compare the different distributions of the genotypes and alleles between patients and healthy controls. The rs2297141 A allele was associated with lower risk of AML compared with the G allele (odds ratio [OR] = 0.704, 95% confidence interval [CI] = 0.503–0.985, P = .04) in both the dominant (OR = 0.447, 95% CI = 0.22–0.909, P = .025, AA vs GG) and recessive inheritance models (OR = 0.419, 95% CI = 0.23–0.763, P = .004, AA vs GA + GG). Although the distribution of the rs6576776 alleles was not different between patients with AML and normal controls, the CC genotype significantly increased the risk of AML in the dominant inheritance model (OR = 6.064, 95% CI = 1.303–28.216, P = .01, CC vs GG) and the recessive inheritance model (OR = 5.937, 95% CI = 1.291–27.306, P = .01, CC vs GC + GG). Additionally, it was shown that the rs2297141 and rs6576776 genotypes were associated with AML-M5 and AML-M2, respectively. Our findings indicated that genetic polymorphisms in the CYR61 gene may be considered potential AML risk factors in the Han Chinese population.
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spelling pubmed-61129682018-09-07 Polymorphisms of the CYR61 gene in patients with acute myeloid leukemia in a Han Chinese population Niu, Chang-Chun Wan, Ya-Fang Yang, Cheng Li, Tian Liao, Pu Medicine (Baltimore) Research Article It was demonstrated in previous studies that cysteine-rich angiogenic inducer 61 (Cyr61) plays vital roles in hematological disorders, and we have already reported that the Cyr61 protein is a tumor promoter in acute myeloid leukemia (AML). Here, we investigated the association between CYR61 gene polymorphisms and susceptibility to AML. We genotyped 2 single-nucleotide polymorphisms (rs2297141 and rs6576776) in the region of the CYR61 gene by improved multiplex ligase detection reaction genotyping assays in a total of 275 samples, including samples from 137 AML patients and 138 healthy controls. Chi-squared tests and logistic regression analysis were performed to compare the different distributions of the genotypes and alleles between patients and healthy controls. The rs2297141 A allele was associated with lower risk of AML compared with the G allele (odds ratio [OR] = 0.704, 95% confidence interval [CI] = 0.503–0.985, P = .04) in both the dominant (OR = 0.447, 95% CI = 0.22–0.909, P = .025, AA vs GG) and recessive inheritance models (OR = 0.419, 95% CI = 0.23–0.763, P = .004, AA vs GA + GG). Although the distribution of the rs6576776 alleles was not different between patients with AML and normal controls, the CC genotype significantly increased the risk of AML in the dominant inheritance model (OR = 6.064, 95% CI = 1.303–28.216, P = .01, CC vs GG) and the recessive inheritance model (OR = 5.937, 95% CI = 1.291–27.306, P = .01, CC vs GC + GG). Additionally, it was shown that the rs2297141 and rs6576776 genotypes were associated with AML-M5 and AML-M2, respectively. Our findings indicated that genetic polymorphisms in the CYR61 gene may be considered potential AML risk factors in the Han Chinese population. Wolters Kluwer Health 2018-08-24 /pmc/articles/PMC6112968/ /pubmed/30142822 http://dx.doi.org/10.1097/MD.0000000000011963 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Niu, Chang-Chun
Wan, Ya-Fang
Yang, Cheng
Li, Tian
Liao, Pu
Polymorphisms of the CYR61 gene in patients with acute myeloid leukemia in a Han Chinese population
title Polymorphisms of the CYR61 gene in patients with acute myeloid leukemia in a Han Chinese population
title_full Polymorphisms of the CYR61 gene in patients with acute myeloid leukemia in a Han Chinese population
title_fullStr Polymorphisms of the CYR61 gene in patients with acute myeloid leukemia in a Han Chinese population
title_full_unstemmed Polymorphisms of the CYR61 gene in patients with acute myeloid leukemia in a Han Chinese population
title_short Polymorphisms of the CYR61 gene in patients with acute myeloid leukemia in a Han Chinese population
title_sort polymorphisms of the cyr61 gene in patients with acute myeloid leukemia in a han chinese population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112968/
https://www.ncbi.nlm.nih.gov/pubmed/30142822
http://dx.doi.org/10.1097/MD.0000000000011963
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