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Tumor Necrosis Factor-A Polymorphisms and Colorectal Cancer Risk: A Meta-Analysis

BACKGROUND AND OBJECTIVES: Tumor necrosis factor-alpha (TNF-a) was related to inflammation and involved in the development of colorectal cancer. Polymorphisms located in TNF-a promoter region, such as 308G/A and 238G/A, could affect the risk of various types of cancer by regulating TNF-a production....

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Autores principales: Min, Li, Chen, Duo, Qu, Like, Shou, Chengchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880329/
https://www.ncbi.nlm.nih.gov/pubmed/24404201
http://dx.doi.org/10.1371/journal.pone.0085187
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author Min, Li
Chen, Duo
Qu, Like
Shou, Chengchao
author_facet Min, Li
Chen, Duo
Qu, Like
Shou, Chengchao
author_sort Min, Li
collection PubMed
description BACKGROUND AND OBJECTIVES: Tumor necrosis factor-alpha (TNF-a) was related to inflammation and involved in the development of colorectal cancer. Polymorphisms located in TNF-a promoter region, such as 308G/A and 238G/A, could affect the risk of various types of cancer by regulating TNF-a production. In this study, a meta-analysis was performed to investigate the association between common polymorphisms of TNF-a promoter region and colorectal cancer susceptibility. METHODS: Searching of several databases was performed for all publications on the association between TNF-a polymorphisms and colorectal cancer. Summary odds ratios (ORs) with their 95% confidence intervals (95% CIs) were calculated using random-effects models. Stratified analyses based on ethnicity and control population source were also conducted. RESULTS: Overall, TNF-a 308A polymorphism showed a significant association with increased risk of colorectal cancer in worldwide populations under homozygote comparison [AA vs. GG, OR (95% CI) = 1.46 (1.07–1.97)] other than heterozygote comparison [AG vs. GG, OR (95% CI) = 1.05 (0.93–1.19)]. TNF-a 238A was not associated with colorectal cancer risk under homozygote or heterozygote comparisons. In stratified analysis, significant association was observed only in Western populations [AA vs. GG, OR (95% CI) = 1.39 (1.01–1.91)] other than in Eastern populations under homozygote comparison. No significant difference was observed between population-based subgroup and hospital-based subgroup. CONCLUSIONS: TNF-a 308A was moderately associated with an increased risk of colorectal cancer in Western populations, and TNF-a 238A polymorphism was not significantly associated with colorectal cancer risk.
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spelling pubmed-38803292014-01-08 Tumor Necrosis Factor-A Polymorphisms and Colorectal Cancer Risk: A Meta-Analysis Min, Li Chen, Duo Qu, Like Shou, Chengchao PLoS One Research Article BACKGROUND AND OBJECTIVES: Tumor necrosis factor-alpha (TNF-a) was related to inflammation and involved in the development of colorectal cancer. Polymorphisms located in TNF-a promoter region, such as 308G/A and 238G/A, could affect the risk of various types of cancer by regulating TNF-a production. In this study, a meta-analysis was performed to investigate the association between common polymorphisms of TNF-a promoter region and colorectal cancer susceptibility. METHODS: Searching of several databases was performed for all publications on the association between TNF-a polymorphisms and colorectal cancer. Summary odds ratios (ORs) with their 95% confidence intervals (95% CIs) were calculated using random-effects models. Stratified analyses based on ethnicity and control population source were also conducted. RESULTS: Overall, TNF-a 308A polymorphism showed a significant association with increased risk of colorectal cancer in worldwide populations under homozygote comparison [AA vs. GG, OR (95% CI) = 1.46 (1.07–1.97)] other than heterozygote comparison [AG vs. GG, OR (95% CI) = 1.05 (0.93–1.19)]. TNF-a 238A was not associated with colorectal cancer risk under homozygote or heterozygote comparisons. In stratified analysis, significant association was observed only in Western populations [AA vs. GG, OR (95% CI) = 1.39 (1.01–1.91)] other than in Eastern populations under homozygote comparison. No significant difference was observed between population-based subgroup and hospital-based subgroup. CONCLUSIONS: TNF-a 308A was moderately associated with an increased risk of colorectal cancer in Western populations, and TNF-a 238A polymorphism was not significantly associated with colorectal cancer risk. Public Library of Science 2014-01-03 /pmc/articles/PMC3880329/ /pubmed/24404201 http://dx.doi.org/10.1371/journal.pone.0085187 Text en © 2014 Min et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Min, Li
Chen, Duo
Qu, Like
Shou, Chengchao
Tumor Necrosis Factor-A Polymorphisms and Colorectal Cancer Risk: A Meta-Analysis
title Tumor Necrosis Factor-A Polymorphisms and Colorectal Cancer Risk: A Meta-Analysis
title_full Tumor Necrosis Factor-A Polymorphisms and Colorectal Cancer Risk: A Meta-Analysis
title_fullStr Tumor Necrosis Factor-A Polymorphisms and Colorectal Cancer Risk: A Meta-Analysis
title_full_unstemmed Tumor Necrosis Factor-A Polymorphisms and Colorectal Cancer Risk: A Meta-Analysis
title_short Tumor Necrosis Factor-A Polymorphisms and Colorectal Cancer Risk: A Meta-Analysis
title_sort tumor necrosis factor-a polymorphisms and colorectal cancer risk: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880329/
https://www.ncbi.nlm.nih.gov/pubmed/24404201
http://dx.doi.org/10.1371/journal.pone.0085187
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