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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doaj-2ebe07c6a35c4c9390c5961ce01d585d2020-11-24T21:45:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0191e8518710.1371/journal.pone.0085187Tumor necrosis factor-a polymorphisms and colorectal cancer risk: a meta-analysis.Li MinDuo ChenLike QuChengchao ShouBACKGROUND 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.http://europepmc.org/articles/PMC3880329?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Li Min Duo Chen Like Qu Chengchao Shou |
spellingShingle |
Li Min Duo Chen Like Qu Chengchao Shou Tumor necrosis factor-a polymorphisms and colorectal cancer risk: a meta-analysis. PLoS ONE |
author_facet |
Li Min Duo Chen Like Qu Chengchao Shou |
author_sort |
Li Min |
title |
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_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_sort |
tumor necrosis factor-a polymorphisms and colorectal cancer risk: a meta-analysis. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2014-01-01 |
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. |
url |
http://europepmc.org/articles/PMC3880329?pdf=render |
work_keys_str_mv |
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