首页> 外文期刊>The Journal of Infectious Diseases >TNF- alpha Promoter Polymorphisms and Susceptibility to Human Papillomavirus 16-Associated Cervical Cancer.
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TNF- alpha Promoter Polymorphisms and Susceptibility to Human Papillomavirus 16-Associated Cervical Cancer.

机译:TNF-α启动子多态性和对人乳头瘤病毒16相关宫颈癌的易感性。

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Background. Polymorphisms in the TNF- alpha promoter region have recently been shown to be associated with susceptibility to cervical cancer. Some polymorphisms have been reported to influence transcription for this cytokine. Altered local levels in the cervix may influence an individual's immune response, thereby affecting persistence of human papillomavirus (HPV) 16 infection, a primary etiological factor for cervical cancer.Methods and Results. The association of 11 TNF- alpha single-nucleotide polymorphisms (SNPs) with susceptibility to HPV16-associated cervical cancer was investigated. Sequencing of the TNF- alpha promoter region confirmed 10 SNPs, and 1 previously unreported SNP (161 bp upstream of the transcriptional start site) was discovered. Microsphere-array flow cytometry-based genotyping was performed on 787 samples from Hispanic and non-Hispanic white women (241 from randomly selected control subjects, 205 from HPV16-positive control subjects, and 341 from HPV16-positive subjects with cervical cancer). The genotype distribution of 3 SNPs (-572, -857, and -863) was significantly different between case subjects and control subjects. Analysis of haplotypes, which were computationally inferred from genotype data, also revealed statistically significant differences in haplotype distribution between case subjects and control subjects.Conclusions. We report new associations between several TNF- alpha SNPs and susceptibility to cervical cancer that support the involvement of the TNF- alpha promoter region in development of cervical cancer.
机译:背景。 TNF-α启动子区域的多态性最近已被证明与子宫颈癌的易感性有关。据报道一些多态性影响该细胞因子的转录。子宫颈局部水平的改变可能会影响个体的免疫反应,从而影响宫颈癌的主要病因-人乳头瘤病毒(HPV)16感染的持续性。方法和结果。研究了11种TNF-α单核苷酸多态性(SNP)与HPV16相关宫颈癌的易感性。 TNF-α启动子区的测序证实了10个SNP,并且发现了1个以前未报道的SNP(转录起始位点上游161bp)。对来自西班牙裔和非西班牙裔白人女性的787个样本(随机抽取的对照组241个,HPV16阳性对照对象205个,宫颈癌HPV16阳性对象341个)进行了787个样本的微球阵列流式细胞分型。 3个SNP(-572,-857和-863)的基因型分布在病例受试者和对照受试者之间存在显着差异。从基因型数据计算得出的单倍型分析也显示病例受试者和对照受试者之间的单倍型分布有统计学上的显着差异。我们报告了几种肿瘤坏死因子-αSNP与宫颈癌的易感性之间的新关联,这支持了肿瘤坏死因子-α启动子区域参与宫颈癌的发展。

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