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TNF-α -308 A allele is associated with an increased risk of distant metastasis in rectal cancer patients from Southwestern China

Tumor necrosis factor-α (TNF-α), an important factor in systematic inflammation, is reportedly involved in several cancer types. The TNF-α -308 G>A (rs1800629) polymorphism in the promoter region influences TNF-α production. The association between TNF-α -308 G>A polymorphism and colorectal ca...

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Autores principales: Li, Zhen, Li, Shu-an, Sun, Ya, Liu, Yu, Li, Wen-liang, Yang, Li, Duan, Yong, Li, Jingyu, Guo, Hao, Zou, Tian-ning, Li, Yunlong, Wang, Kun-hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456043/
https://www.ncbi.nlm.nih.gov/pubmed/28575042
http://dx.doi.org/10.1371/journal.pone.0178218
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author Li, Zhen
Li, Shu-an
Sun, Ya
Liu, Yu
Li, Wen-liang
Yang, Li
Duan, Yong
Li, Jingyu
Guo, Hao
Zou, Tian-ning
Li, Yunlong
Wang, Kun-hua
author_facet Li, Zhen
Li, Shu-an
Sun, Ya
Liu, Yu
Li, Wen-liang
Yang, Li
Duan, Yong
Li, Jingyu
Guo, Hao
Zou, Tian-ning
Li, Yunlong
Wang, Kun-hua
author_sort Li, Zhen
collection PubMed
description Tumor necrosis factor-α (TNF-α), an important factor in systematic inflammation, is reportedly involved in several cancer types. The TNF-α -308 G>A (rs1800629) polymorphism in the promoter region influences TNF-α production. The association between TNF-α -308 G>A polymorphism and colorectal cancer (CRC) is not fully understood, especially the connections between TNF-α -308 G>A polymorphism and clinical features of CRC. In this study, TNF-α -308 G>A polymorphism was genotyped in 1140 individuals with or without CRC from Southwestern China. In case-control studies, we found no association between TNF-α -308 G>A polymorphism and CRC risk. Analysis of the correlations between TNF-α -308 G>A polymorphism and clinical features of CRC revealed that TNF-α -308 A allele was associated with higher body mass index (BMI) larger tumor size, and distant tumor metastasis in all CRC patients. Notably, rectal cancer (a subtype of CRC) patients with TNF-α -308 A allele had a very high risk of distant tumor metastasis [odds ratio (OR) = 4.481; 95% confidence interval (CI): 2.072–9.693; P = 0.00025]. The association between TNF-α -308 A allele and distant tumor metastasis remained even significant after adjusting all clinical characteristics (OR = 7.099; 95% CI: 2.482–20.301; P = 0.000256) in rectal cancer patients. Our results suggested that TNF-α -308 A allele was significantly associated with distant tumor metastasis in rectal cancer patients.
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spelling pubmed-54560432017-06-12 TNF-α -308 A allele is associated with an increased risk of distant metastasis in rectal cancer patients from Southwestern China Li, Zhen Li, Shu-an Sun, Ya Liu, Yu Li, Wen-liang Yang, Li Duan, Yong Li, Jingyu Guo, Hao Zou, Tian-ning Li, Yunlong Wang, Kun-hua PLoS One Research Article Tumor necrosis factor-α (TNF-α), an important factor in systematic inflammation, is reportedly involved in several cancer types. The TNF-α -308 G>A (rs1800629) polymorphism in the promoter region influences TNF-α production. The association between TNF-α -308 G>A polymorphism and colorectal cancer (CRC) is not fully understood, especially the connections between TNF-α -308 G>A polymorphism and clinical features of CRC. In this study, TNF-α -308 G>A polymorphism was genotyped in 1140 individuals with or without CRC from Southwestern China. In case-control studies, we found no association between TNF-α -308 G>A polymorphism and CRC risk. Analysis of the correlations between TNF-α -308 G>A polymorphism and clinical features of CRC revealed that TNF-α -308 A allele was associated with higher body mass index (BMI) larger tumor size, and distant tumor metastasis in all CRC patients. Notably, rectal cancer (a subtype of CRC) patients with TNF-α -308 A allele had a very high risk of distant tumor metastasis [odds ratio (OR) = 4.481; 95% confidence interval (CI): 2.072–9.693; P = 0.00025]. The association between TNF-α -308 A allele and distant tumor metastasis remained even significant after adjusting all clinical characteristics (OR = 7.099; 95% CI: 2.482–20.301; P = 0.000256) in rectal cancer patients. Our results suggested that TNF-α -308 A allele was significantly associated with distant tumor metastasis in rectal cancer patients. Public Library of Science 2017-06-02 /pmc/articles/PMC5456043/ /pubmed/28575042 http://dx.doi.org/10.1371/journal.pone.0178218 Text en © 2017 Li 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Li, Zhen
Li, Shu-an
Sun, Ya
Liu, Yu
Li, Wen-liang
Yang, Li
Duan, Yong
Li, Jingyu
Guo, Hao
Zou, Tian-ning
Li, Yunlong
Wang, Kun-hua
TNF-α -308 A allele is associated with an increased risk of distant metastasis in rectal cancer patients from Southwestern China
title TNF-α -308 A allele is associated with an increased risk of distant metastasis in rectal cancer patients from Southwestern China
title_full TNF-α -308 A allele is associated with an increased risk of distant metastasis in rectal cancer patients from Southwestern China
title_fullStr TNF-α -308 A allele is associated with an increased risk of distant metastasis in rectal cancer patients from Southwestern China
title_full_unstemmed TNF-α -308 A allele is associated with an increased risk of distant metastasis in rectal cancer patients from Southwestern China
title_short TNF-α -308 A allele is associated with an increased risk of distant metastasis in rectal cancer patients from Southwestern China
title_sort tnf-α -308 a allele is associated with an increased risk of distant metastasis in rectal cancer patients from southwestern china
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456043/
https://www.ncbi.nlm.nih.gov/pubmed/28575042
http://dx.doi.org/10.1371/journal.pone.0178218
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