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作 者:尉春艳[1] 吴静[1] 张熙[2] 张菊[3] 高艳娥[1]
机构地区:[1]西安交通大学医学院第二附属医院妇产科,陕西西安710004 [2]西安交通大学医学院第一附属医院神经外科,陕西西安710061 [3]第四军医大学基因诊断技术研究所,陕西西安710033
出 处:《西安交通大学学报(医学版)》2009年第2期225-228,243,共5页Journal of Xi’an Jiaotong University(Medical Sciences)
摘 要:目的探讨TNFα基因-863位点的单核苷酸多态性与宫颈癌以及HPV感染的关系。方法采用模板介导的染料终止物掺入一荧光偏振检测(TDI-FP)的方法对59例宫颈癌以及22例对照进行TNFα基因一863位点的单核苷酸多态性检测。结果宫颈癌组的TNFα基因-863位点A等位基因频率(39.0%)较对照组(14.6%)明显升高(P〈0.01,OR=2.673,95%CI:1.300~5.497);AA基因型在宫颈癌组和对照组中分别为15.3%和0,差异显著(P〈0.05);CA基因型在两组中分别为47.5%和29.2%,差异显著(P〈O.05);A等位基因频率在HPV阳性者与HPV阴性者之间没有显著性差异(P〉0.05,OR:1.950,95%CI:0.840~4.527),但是在HPV阳性者中具有增高趋势(37.5%),高于HPV阴性者(19.2%)。结论TNFα基因863位点A等位基因以及CA、AA基因型与宫颈癌的危险性升高有关,与HPV感染危险性无关。Objective To analyze the relationship between cervical cancer, and the polymorphism of tumor necrosis factor α (TNFα) gene at the site of -863. Methods TDI-FP was adopted to detect the polymorphism of TNFα gene at the site of -863 in 59 cases and 22 controls. Results The positive rate of A allele at -863 in group of cervical cancer (39.0 % ) was significantly higher than that in control group (14.6 % ) (P〈0.01, OR = 2. 673, 95% CI : 1. 300- 5.497). Genotypes of CA and AA were 47.5 % and 15.3 % in cases of cervical cancer, and significantly low rates of 29.2% and 0% in cases of control, respectively (P〈0. 05). Although no significant difference (P〉0. 05, OR =1. 950, 95% CI: 0. 840-4. 527) was found between HPV positive and negative groups, a trend of high positive rate of A allele at -863 in HPV positive group was found. Conclusion The A allele, AA genotypes and CA genotypes at -863 of TNFα gene is associated significantly with increased risk of cervical cancer. Polymorphism at -863 does not attribute to HPV infection.
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