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Association of Interferon Gamma +874T/A Polymorphism and Leukemia Risk: A Meta-Analysis

Interferon gamma (IFN-γ) has antitumor and antiproliferative effects, and previous studies indicated IFN-γ +874T/A (rs2430561) polymorphism were related to the risk of many types of cancer. However, the association between IFN-γ +874T/A polymorphism and leukemia risk remained controversial. We perfo...

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Autores principales: Wu, Zhitong, Sun, Yifan, Zhu, Shengbo, Tang, Shifu, Liu, Chunming, Qin, Wenzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998384/
https://www.ncbi.nlm.nih.gov/pubmed/27015189
http://dx.doi.org/10.1097/MD.0000000000003129
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author Wu, Zhitong
Sun, Yifan
Zhu, Shengbo
Tang, Shifu
Liu, Chunming
Qin, Wenzhou
author_facet Wu, Zhitong
Sun, Yifan
Zhu, Shengbo
Tang, Shifu
Liu, Chunming
Qin, Wenzhou
author_sort Wu, Zhitong
collection PubMed
description Interferon gamma (IFN-γ) has antitumor and antiproliferative effects, and previous studies indicated IFN-γ +874T/A (rs2430561) polymorphism were related to the risk of many types of cancer. However, the association between IFN-γ +874T/A polymorphism and leukemia risk remained controversial. We performed a comprehensive meta-analysis based on the Preferred Reporting Items for Systematic Reviews and Meta-analyses statement (PRISMA). Electronic database of Embase, Pubmed, and the Cochrane Library were searched for eligible articles published up to December 13, 2015. The association between genetic polymorphisms and leukemia risk was measured by odds ratios (ORs) and its corresponding 95% confidence intervals (CIs). A total of 8 studies amounting to 420 patients and 767 control subjects were retrieved for this study. Although associations between IFN-γ +874T/A polymorphism and overall leukemia risks were lacking, decreased chronic lymphocytic leukemia (CLL) risk was detected in the allelic model (T vs A, OR=0.660, 95%CI = 0.483–0.902, P = 0.009, I(2) = 0.0% and P = 0.863 for heterogeneity), the codominant model (TT vs AA, OR = 0.472, 95%CI = 0.247–0.902, P = 0.023, I(2) = 0.0% and P = 0.994 for heterogeneity), and dominant model (TT + TA vs AA, OR = 0.457, 95%CI = 0.285–0.734, P = 0.001, I(2) = 40.3% and P = 0.195 for heterogeneity) by using fixed-effect model separately. On the contrary, results indicated T carries have an increased chronic myelogenous leukemia (CML) risk in dominant model (TT + TA vs AA, OR = 1.783, 95%CI = 1.236–2.573, P = 0.002, I(2) = 19.0% and P = 0.295 for heterogeneity). This study suggests IFN-γ +874T/A polymorphism are related to CML and CLL risk. In addition, our work also points out IFN-γ +874T/A polymorphism may play dual contrasting role in leukemia risk.
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spelling pubmed-49983842016-09-02 Association of Interferon Gamma +874T/A Polymorphism and Leukemia Risk: A Meta-Analysis Wu, Zhitong Sun, Yifan Zhu, Shengbo Tang, Shifu Liu, Chunming Qin, Wenzhou Medicine (Baltimore) 3500 Interferon gamma (IFN-γ) has antitumor and antiproliferative effects, and previous studies indicated IFN-γ +874T/A (rs2430561) polymorphism were related to the risk of many types of cancer. However, the association between IFN-γ +874T/A polymorphism and leukemia risk remained controversial. We performed a comprehensive meta-analysis based on the Preferred Reporting Items for Systematic Reviews and Meta-analyses statement (PRISMA). Electronic database of Embase, Pubmed, and the Cochrane Library were searched for eligible articles published up to December 13, 2015. The association between genetic polymorphisms and leukemia risk was measured by odds ratios (ORs) and its corresponding 95% confidence intervals (CIs). A total of 8 studies amounting to 420 patients and 767 control subjects were retrieved for this study. Although associations between IFN-γ +874T/A polymorphism and overall leukemia risks were lacking, decreased chronic lymphocytic leukemia (CLL) risk was detected in the allelic model (T vs A, OR=0.660, 95%CI = 0.483–0.902, P = 0.009, I(2) = 0.0% and P = 0.863 for heterogeneity), the codominant model (TT vs AA, OR = 0.472, 95%CI = 0.247–0.902, P = 0.023, I(2) = 0.0% and P = 0.994 for heterogeneity), and dominant model (TT + TA vs AA, OR = 0.457, 95%CI = 0.285–0.734, P = 0.001, I(2) = 40.3% and P = 0.195 for heterogeneity) by using fixed-effect model separately. On the contrary, results indicated T carries have an increased chronic myelogenous leukemia (CML) risk in dominant model (TT + TA vs AA, OR = 1.783, 95%CI = 1.236–2.573, P = 0.002, I(2) = 19.0% and P = 0.295 for heterogeneity). This study suggests IFN-γ +874T/A polymorphism are related to CML and CLL risk. In addition, our work also points out IFN-γ +874T/A polymorphism may play dual contrasting role in leukemia risk. Wolters Kluwer Health 2016-03-25 /pmc/articles/PMC4998384/ /pubmed/27015189 http://dx.doi.org/10.1097/MD.0000000000003129 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 3500
Wu, Zhitong
Sun, Yifan
Zhu, Shengbo
Tang, Shifu
Liu, Chunming
Qin, Wenzhou
Association of Interferon Gamma +874T/A Polymorphism and Leukemia Risk: A Meta-Analysis
title Association of Interferon Gamma +874T/A Polymorphism and Leukemia Risk: A Meta-Analysis
title_full Association of Interferon Gamma +874T/A Polymorphism and Leukemia Risk: A Meta-Analysis
title_fullStr Association of Interferon Gamma +874T/A Polymorphism and Leukemia Risk: A Meta-Analysis
title_full_unstemmed Association of Interferon Gamma +874T/A Polymorphism and Leukemia Risk: A Meta-Analysis
title_short Association of Interferon Gamma +874T/A Polymorphism and Leukemia Risk: A Meta-Analysis
title_sort association of interferon gamma +874t/a polymorphism and leukemia risk: a meta-analysis
topic 3500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998384/
https://www.ncbi.nlm.nih.gov/pubmed/27015189
http://dx.doi.org/10.1097/MD.0000000000003129
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