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作 者:张莉[1] 吴素慧[1] 尚海霞[1] 唐世倩[1] 林维凤[1]
机构地区:[1]山西医科大学第一医院妇产科,太原030001
出 处:《肿瘤研究与临床》2010年第6期404-405,409,共3页Cancer Research and Clinic
基 金:山西省自然科学基金(2006011121);山西省科技攻关项目(2007031091-6)
摘 要:目的 探讨白细胞介素(IL)-8-251A/T单核苷酸多态性与子宫颈癌发病的相关性.方法 应用四引物扩增受阻突变体系-聚合酶链反应技术(Tetra-primer ARMS-PCR)分析217例子宫颈癌患者和190例健康对照者外周血IL-8-251A/T位点的基因多态性,用Logistic回归模型计算各种基因型的子宫颈癌风险(OR)及其95%可信区间.结果 IL-8-251A/T单核苷酸多态性三种基因型在病例组分别为18.89%、53.46%、27.65%,对照组则分别为35.79%、44.21%、20.00%,两组差异有统计学意义(P〈0.05) TT基因型及T等位基因的子宫颈癌发病OR分别为2.619、1.639.结论 IL-8.251A/T基因多态性可能是子宫颈癌发病的遗传易感因素.Objective To investigate the relationship between single nucleotide polymorphisms of IL-8-251 A/T and the occurrence of cervical cancer.Methods A retrospective case-control study design Was applied for the present study.The cage group included peripheral blood samples from 217 cervical cancer patients and peripheral blood samples from 190 healthy women.Tetra-primer amplification refractory mutation system polymerase chain reaction Was used to analyze the genotype distribution and allele frequency of IL-8-251 A/T.Results It-8-251 MT gene polymowhisms included three genotypes:AA,AT and TT.Proportions of genotypes were 18.89%,53.46%,27.65%in cage group,respectively and were 35.79%,44.21%,20.00%in control group,respectively.There was statistical significance(P〈0.05)between the case group and the control group.The risk of genotype TT and T allele for cervical cancer Wag 2.619 and 1.639.respectively.Conclusion IL-8-25 1 A/T may be a genetic susceptibility factors for cervical cancer.
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