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IL-1B rs2853550 polymorphism contributes to esophageal cancer susceptibility in Chinese Han population of Northwest China

机译:IL-1B RS2853550多态性导致中国西北部中国汉族人口食管癌易感性有助于

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Esophageal 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. In 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. A 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. This study demonstrated that rs2853550 in IL-1B might increase EC susceptibility in the Chinese Han population of Northwest China.
机译:食管癌(EC)是最常见的人类癌症之一,具有特别侵略性的行为和全世界发病率增加。本研究的目的是评估IL-1B中单核苷酸多态性(SNPS)在西北汉族人口中欧洲危险的危险。为了评估IL-1B多态性和EC风险之间的相关性,Agena MassArray平台用于确定384例患者和499例对照中候选SNP的基因型。通过调整性别和年龄的调整,检查IL-1B变体和EC风险之间的关联。进行单倍型构建和分析以检测IL-1B和EC易感性单倍型之间的潜在关联。另外,生物信息学数据库用于基因表达分析和SNP功能预测。在IL-1B RS2853550之间发现了一个重要的关系和等位基因模型中的EC的风险增加[赔率比(或)?=?1.38,95%置信区间(95%CI):1.01-1.89,P?=?0.041 ),Codominant模型(A / g,或α=?1.63,95%CI:1.10-2.42,P?=?0.011)和主导模型(或?=?1.49,95%CI:1.02-2.18, p?= 0.041)。功能分析揭示了RS2853550的潜在影响,这进一步加强了对EC易感性的影响。然而,EC病例和健康对照之间的其他SNP或单倍型没有统计学意义差异。用数据集进行的表达分析表明EC-1B的表达水平在EC病例中比正常样品更高。本研究表明,IL-1B的RS2853550可能会增加中国西北部中国汉族人群的EC易感性。

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