摘要
目的:探讨维生素D受体(VDR)基因Fok I位点多态性与原发性肝癌遗传易感性的关系。方法:采用聚合酶链限制性片段长度多态性分析和基因测序技术,对105例原发性肝癌患者和100例健康体检者VDR基因Fok I位点的多态性进行分析。结果:原发性肝癌患者Fok I位点ff基因型频率明显高于健康体检者。与FF基因型相比,ff基因型患原发性肝癌的风险性增加(OR=2.241,P<0.05);与F等位基因相比,携带f等位基因的个体更易罹患原发性肝癌(OR=1.479,P<0.05)。结论:VDR基因Fok I位点多态性可能是原发性肝癌发生的遗传易感因素之一。
Objective: To investigate the relationships between Fok I site polymorphism of vitamin D receptor(VDR) and hereditary susceptibility of primary hepatic carcinoma. Methods: Polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) and genetic sequencing technology were used to detect polymorphisms of VDR gene Fok I site polymorphism of 105 primary hepatic carcinoma patients and 100 healthy controls. Results: The Fok I site ff genotype frequency of primary hepatic carcinoma patients was obviously higher than healthy controls. Compared with FF genotype, the ff genotype increased the risk of suffering primary hepatic carcinoma(OR=2.241, P〈0.05). Compared with F allele, the individuals carrying f alleles were more prone to primary hepatic carcinoma(OR=1.479, P〈0.05). Conclusions: The VDR gene Fok I site polymorphism maybe one of the genetic susceptibility factors of primary hepatic carcinoma.
出处
《承德医学院学报》
2015年第5期369-371,共3页
Journal of Chengde Medical University
基金
广西壮族自治区卫生厅科研自筹课题基金资助项目(Z2014418)
关键词
维生素D受体
基因多态性
原发性肝癌
遗传易感性
Vitamin D receptor
Gene polymorphism
Primary hepatic carcinoma
Hereditary susceptibility