Oncotarget

Meta-Analysis:

Genetic association between TNF-α promoter polymorphism and susceptibility to squamous cell carcinoma, basal cell carcinoma, and melanoma: A meta-analysis

Ning Liu _, Guang-Jing Liu and Juan Liu

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Oncotarget. 2017; 8:53873-53885. https://doi.org/10.18632/oncotarget.17179

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Abstract

Ning Liu1, Guang-Jing Liu1 and Juan Liu2

1Department of Plastic and Burns Surgery, The First Center Hospital of Tianjin, Tianjin 300192, PR China

2Department of General Surgery, Bailou Hospital, Tianjin 300040, PR China

Correspondence to:

Ning Liu, email: nick_joan_tj@163.com

Keywords: TNF-α, single nucleotide polymorphism, SCC, BCC, melanoma

Received: December 19, 2016     Accepted: March 16, 2017     Published: April 18, 2017

ABSTRACT

Tumor necrosis factor-alpha (TNF-α) is a multifunctional pro-inflammatory cytokine that plays an important role in cancer development. We performed a meta-analysis to assess the relationship between single nucleotide polymorphisms in the TNF-α promoter region (rs1800629 and rs361525) and susceptibility to squamous cell carcinoma (SCC), basal cell carcinoma (BCC) and melanoma. After database retrieval, article selection, data extraction, and quality assessment, 20 articles comprising 4865 cases and 6329 controls were included in this study. rs1800629 was associated with an increased overall risk of SCC, lung SCC, and oral SCC in the AA vs G and AA vs GG+GA genetic models (all OR>1, Passociation<0.05). No increased risk of skin SCC, skin BCC or melanoma was observed (all Passociation>0.05). Rs361525 was not associated with overall SCC risk in the allele, heterozygote, dominant, recessive, or carrier model (all Passociation>0.05). Begg’s and Egger’s tests (PBegg>0.05; PEgger>0.05) demonstrated there was no significant publication bias. These data indicate that the AA genotype of TNF-α rs1800629, but not rs361525, is associated with an increased risk of SCC, suggesting it could potentially serve as a prognostic marker for predicting SCC risk.


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