首页> 外文期刊>Molecular Genetics & Genomic Medicine >The impact of genetic variants in IL1R2 on cervical cancer risk among Uygur females from China: A case–control study
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The impact of genetic variants in IL1R2 on cervical cancer risk among Uygur females from China: A case–control study

机译:IL1R2基因变异对中国维吾尔族女性宫颈癌风险的影响:病例对照研究

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Background Disordered inflammation and immune response is an acknowledged risk factor for cervical cancer development. Interleukin‐1 receptor type 2 (IL1R2) is a decoy receptor for IL‐1 cytokines and involved in host inflammatory and immune progression which could lead to the lesion and neoplasia of cervix. In this study, we aimed to evaluate the relationships between IL1R2 polymorphisms and cervical cancer risk in Uygur females from China. Methods In this case–control study, genotypes of six selected variants (rs11674595, rs4851527, rs719250, rs3218896, rs3218977, and rs2072472) distributed in IL1R2 were detected among 247 cervical cancer patients and 286 healthy controls with the usage of an Agena MassARRY method. Furthermore, Genetic models and haplotype analyses were conducted to estimate the associations of IL1R2 polymorphisms with cervical cancer risk. Results After statistical analyses, rs719250 (odd ratio [OR]?=?1.436, 95% confidence interval [95% CI]?=?1.079–1.911, p ?=?0.013) and rs3218896 (OR?=?1.552, 95% CI?=?1.080–2.229, p ?=?0.017) showed obvious evidence in correlation to cervical cancer susceptibility owing to the surviving significant differences between cases and controls in allele model. Genetic model analyses also revealed significant associations of rs719250 and rs3218896 with cervical cancer risk in the codominant model, the dominant model and the log‐additive model even after adjustment for age ( p ??0.05). Moreover, haplotype “T/A” of rs11674595/rs4851527 (adjusted OR?=?0.73, 95% CI?=?0.54–0.98, p ?=?0.037) and “T/C” of rs719250/rs3218896 (adjusted OR?=?1.61, 95% CI?=?1.10–2.36, p ?=?0.015) exhibited protective and risky effects for Uygur individuals on cervical cancer development, respectively. Conclusion Our data first shed the new light on the associations of IL1R2 polymorphisms with cervical cancer susceptibility among Uygur females. These results are supposed to facilitate the tumorigenesis genetic research among Chinese minorities.
机译:背景炎症和免疫反应异常是宫颈癌发展的公认危险因素。 2型白介素-1受体(IL1R2)是IL-1细胞因子的诱饵受体,参与宿主的炎症和免疫进程,可能导致子宫颈的病变和赘生物。在这项研究中,我们旨在评估中国维吾尔族女性IL1R2多态性与宫颈癌风险之间的关系。方法在本病例对照研究中,使用Agena MassARRY方法,在247例宫颈癌患者和286例健康对照中检测了分布在IL1R2中的六个选定变体(rs11674595,rs4851527,rs719250,rs3218896,rs3218977和rs2072472)的基因型。此外,进行了遗传模型和单倍型分析,以估计IL1R2多态性与宫颈癌风险的关系。结果经过统计分析,rs719250(奇数比[OR]?=?1.436,95%置信区间[95%CI]?=?1.079-1.911,p?=?0.013)和rs3218896(OR?=?1.552,95% CI?=?1.080–2.229,p?=?0.017)显示了与宫颈癌易感性相关的明显证据,这是由于病例与对照组之间在等位基因模型中尚存显着差异。遗传模型分析还显示,即使在调整了年龄之后,在共显性模型,显性模型和对数加性模型中,rs719250和rs3218896与子宫颈癌风险之间也存在显着关联(p≤0.05)。此外,rs11674595 / rs4851527的单倍型“ T / A”(调整为OR?=?0.73,95%CI?=?0.54-0.98,p?=?0.037)和rs719250 / rs3218896的“ T / C”(调整为OR?)。 =?1.61,95%CI?=?1.10–2.36,p?=?0.015)分别对维吾尔族个体具有宫颈癌发展的保护作用和危险作用。结论我们的数据首先为维吾尔族女性中IL1R2基因多态性与宫颈癌易感性的关系提供了新的认识。这些结果被认为有助于中国少数民族的肿瘤发生遗传学研究。

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