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ABCB1 C3435T polymorphism is associated with leukemia susceptibility: evidence from a meta-analysis

INTRODUCTION AND OBJECTIVE: Many studies have been conducted on the association between the adenosine triphosphate-binding cassette, subfamily B, member 1 (ABCB1) gene C3435T polymorphism and leukemia risk, however, the previously published findings remain controversial. Thus, a meta-analysis was ca...

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Autores principales: Ma, Limin, Ruan, Linhai, Liu, Hongchao, Yang, Haiping, Feng, Yanming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427449/
https://www.ncbi.nlm.nih.gov/pubmed/25999734
http://dx.doi.org/10.2147/OTT.S82144
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author Ma, Limin
Ruan, Linhai
Liu, Hongchao
Yang, Haiping
Feng, Yanming
author_facet Ma, Limin
Ruan, Linhai
Liu, Hongchao
Yang, Haiping
Feng, Yanming
author_sort Ma, Limin
collection PubMed
description INTRODUCTION AND OBJECTIVE: Many studies have been conducted on the association between the adenosine triphosphate-binding cassette, subfamily B, member 1 (ABCB1) gene C3435T polymorphism and leukemia risk, however, the previously published findings remain controversial. Thus, a meta-analysis was carried out to accurately evaluate the effect of this polymorphism on leukemia susceptibility. METHODS: A computerized literature search was conducted of PubMed, Elsevier database, the China National Knowledge Infrastructure database, and Wanfang Database, to find published case–control studies exploring the relationship between ABCB1 C3435T polymorphism and leukemia risk. Odds ratios (ORs) with 95% confidence intervals (CIs) were applied to assess the strength of association. RESULTS: A total of 17 studies of 2,431 cases and 3,028 controls were included in this meta-analysis. The results of overall comparisons suggest that there is a significant association between ABCB1 C3435T polymorphism and leukemia risk under two genetic models (TT vs CC: OR=1.39, 95% CI=1.04–1.84, P=0.02; CT+TT vs CC: OR=1.20, 95% CI=1.06–1.36, P=0.004). In the subgroup analyses by ethnicity, age, and leukemia subtype, a significant association was found in Caucasian (CT vs CC: OR=1.22, 95% CI=1.03–1.45, P=0.02; TT vs CC: OR=1.34, 95% CI=1.10–1.64, P=0.004; CT+TT vs CC: OR=1.27, 95% CI=1.08–1.49, P=0.004), adult leukemia (CT vs CC: OR=1.46, 95% CI=1.17–1.83, P=0.001; CT+TT vs CC: OR=1.43, 95% CI=1.01–2.03, P=0.04), and lymphocytic leukemia (TT vs CC: OR=1.73, 95% CI=1.19–2.51, P=0.004; TT vs CC+CT: OR=1.62, 95% CI=1.10–2.38, P=0.01; CT+TT vs CC: OR=1.28, 95% CI=1.10–1.48, P=0.001). CONCLUSION: The meta-analysis suggests that ABCB1 C3435T polymorphism is associated with increased risk of leukemia.
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spelling pubmed-44274492015-05-21 ABCB1 C3435T polymorphism is associated with leukemia susceptibility: evidence from a meta-analysis Ma, Limin Ruan, Linhai Liu, Hongchao Yang, Haiping Feng, Yanming Onco Targets Ther Original Research INTRODUCTION AND OBJECTIVE: Many studies have been conducted on the association between the adenosine triphosphate-binding cassette, subfamily B, member 1 (ABCB1) gene C3435T polymorphism and leukemia risk, however, the previously published findings remain controversial. Thus, a meta-analysis was carried out to accurately evaluate the effect of this polymorphism on leukemia susceptibility. METHODS: A computerized literature search was conducted of PubMed, Elsevier database, the China National Knowledge Infrastructure database, and Wanfang Database, to find published case–control studies exploring the relationship between ABCB1 C3435T polymorphism and leukemia risk. Odds ratios (ORs) with 95% confidence intervals (CIs) were applied to assess the strength of association. RESULTS: A total of 17 studies of 2,431 cases and 3,028 controls were included in this meta-analysis. The results of overall comparisons suggest that there is a significant association between ABCB1 C3435T polymorphism and leukemia risk under two genetic models (TT vs CC: OR=1.39, 95% CI=1.04–1.84, P=0.02; CT+TT vs CC: OR=1.20, 95% CI=1.06–1.36, P=0.004). In the subgroup analyses by ethnicity, age, and leukemia subtype, a significant association was found in Caucasian (CT vs CC: OR=1.22, 95% CI=1.03–1.45, P=0.02; TT vs CC: OR=1.34, 95% CI=1.10–1.64, P=0.004; CT+TT vs CC: OR=1.27, 95% CI=1.08–1.49, P=0.004), adult leukemia (CT vs CC: OR=1.46, 95% CI=1.17–1.83, P=0.001; CT+TT vs CC: OR=1.43, 95% CI=1.01–2.03, P=0.04), and lymphocytic leukemia (TT vs CC: OR=1.73, 95% CI=1.19–2.51, P=0.004; TT vs CC+CT: OR=1.62, 95% CI=1.10–2.38, P=0.01; CT+TT vs CC: OR=1.28, 95% CI=1.10–1.48, P=0.001). CONCLUSION: The meta-analysis suggests that ABCB1 C3435T polymorphism is associated with increased risk of leukemia. Dove Medical Press 2015-05-05 /pmc/articles/PMC4427449/ /pubmed/25999734 http://dx.doi.org/10.2147/OTT.S82144 Text en © 2015 Ma et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Ma, Limin
Ruan, Linhai
Liu, Hongchao
Yang, Haiping
Feng, Yanming
ABCB1 C3435T polymorphism is associated with leukemia susceptibility: evidence from a meta-analysis
title ABCB1 C3435T polymorphism is associated with leukemia susceptibility: evidence from a meta-analysis
title_full ABCB1 C3435T polymorphism is associated with leukemia susceptibility: evidence from a meta-analysis
title_fullStr ABCB1 C3435T polymorphism is associated with leukemia susceptibility: evidence from a meta-analysis
title_full_unstemmed ABCB1 C3435T polymorphism is associated with leukemia susceptibility: evidence from a meta-analysis
title_short ABCB1 C3435T polymorphism is associated with leukemia susceptibility: evidence from a meta-analysis
title_sort abcb1 c3435t polymorphism is associated with leukemia susceptibility: evidence from a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427449/
https://www.ncbi.nlm.nih.gov/pubmed/25999734
http://dx.doi.org/10.2147/OTT.S82144
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