Abstract

BackgroundEsophageal cancer (EC) is one of the most common human cancers, with a particularly aggressive behavior and increased incidence worldwide. The aim of this study was to assess the associations of single-nucleotide polymorphisms (SNPs) in IL-1B with the risk of EC in a northwest Chinese Han population.MethodsIn order to evaluate the correlations between IL-1B polymorphisms and EC risk, an Agena MassARRAY platform was used to determine the genotype of the candidate SNPs among 384 EC patients and 499 controls. The associations between IL-1B variants and EC risk were examined using logistic regression analysis with adjustment for gender and age. Haplotype construction and analysis were performed to detect the potential associations between haplotypes within IL-1B and EC susceptibility. Additionally, bioinformatics databases were used for gene expression analysis and SNP functional prediction.ResultsA significant relationship was found between IL-1B rs2853550 and an increased risk of EC in the allele model [odds ratio (OR) = 1.38, 95% confidence interval (95% CI): 1.01–1.89, p = 0.041), the codominant model (A/G, OR = 1.63, 95% CI: 1.10–2.42, p = 0.011), and the dominant model (OR = 1.49, 95% CI: 1.02–2.18, p = 0.041). Functional analysis revealed the potential effects of rs2853550, which further reinforced its influence on EC susceptibility. However, there were no statistically significant differences for other SNPs or haplotypes between EC cases and healthy controls. Expression analysis conducted with dataset indicated that the expression level of IL-1B was higher in EC cases than that in normal samples.ConclusionsThis study demonstrated that rs2853550 in IL-1B might increase EC susceptibility in the Chinese Han population of Northwest China.

Highlights

  • Esophageal cancer (EC) is one of the most common human cancers, with a aggressive behavior and increased incidence worldwide

  • We aimed to investigate the relationships between seven singlenucleotide polymorphisms (SNPs) within IL-1B, namely rs2853550, rs1143643, rs3136558, rs1143630, rs1143627, rs16944, and rs1143623, and the risk of EC in a Han population from northwest China

  • We evaluated the correlation between the IL-1B SNPs and EC susceptibility using four genetic models, hypothesizing that the minor allele of each variant was a risk factor

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Summary

Introduction

Esophageal cancer (EC) is one of the most common human cancers, with a aggressive behavior and increased incidence worldwide. The aim of this study was to assess the associations of singlenucleotide polymorphisms (SNPs) in IL-1B with the risk of EC in a northwest Chinese Han population. Esophageal cancer (EC) is the eighth most common human cancer, and its incidence rate has significantly increased in recent years (Parkin et al 2005). Previous studies have uncovered several significant IL1B polymorphisms associated with diverse diseases in different cohorts worldwide. Majeed et al have found a common polymorphic allele in the regulatory region of IL-1B that is associated with increased production of IL-1β in cervical lesions among European females (Majeed et al 1999). IL-1B variants have been proved to be associated with gastric cancer susceptibility (He et al 2011a) and inflammatory bowel disease (Nemetz et al 1999)

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