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机构地区:[1]安徽省来安县人民医院影像科,239200 [2]安徽省来安县家宁医院外科,239200 [3]江苏省东南大学附属中大医院普外科,江苏南京210009
出 处:《蚌埠医学院学报》2016年第2期152-154,158,共4页Journal of Bengbu Medical College
摘 要:目的:研究BRM-741位点和BRM-1321位点的插入/缺失多态与中国汉族人群食管鳞状细胞癌(ESCC)易感性的关系。方法:采用病例-对照研究,以聚合酶链反应-聚丙烯酰胺凝胶电泳的方法,分析343例ESCC患者和362名性别、年龄等人口学特征与病例频数匹配的健康对照者的BRM-741以及BRM-1321基因型分布情况。logistic回归分析BRM基因多态与ESCC易感性的关系。结果:BRM-741多态与ESCC的患病风险无相关性(P〉0.05),而BRM-1321多态与ESCC的发生有相关性(P〈0.01)。携带BRM-1321插入/插入基因型的个体发生ESCC的风险较携带BRM-1321缺失/缺失基因型者增加了94.0%(OR=1.94,95%CI=1.11~3.38)。与缺失型等位基因比较,插入型等位基因增加了35.0%的ESCC易感性(OR=1.35,95%CI=1.07~1.71)。结论:BRM-1321多态与中国汉族人群ESCC遗传易感性有关,BRM-741基因多态与中国汉族人群ESCC的患病风险无关。Objective: To investigate the association of indel polymorphisms of BRM-741 and BRM-132 with the susceptibility of esophageal squamous cell carcinoma( ESCC) in Chinese Han population. Methods: The genotype distribution of BRM-741 and BRM-1321 in 343 cases of ESCC and 362 healthy controls whose gender,age and other demographic characteristics were matched with the frequency of the ESCC cases was analyzed in a case-control study by using polymerase chain reaction-polyacrylamide gel electrophoresis method. Logistic regression model was used to evaluate the association between polymorphisms and ESCC susceptibility. Results: There was no significant association between BRM-741 and ESCC( P 〉0. 05). However,there was a significant association between BRM-1321 and ESCC susceptibility( P 〈0. 01). The insertion / insertion genotype was associated with an increased risk of ESCC compared with the deletion / deletion genotype of BRM 1321( OR = 1. 94,95% CI = 1. 11- 3. 38). The insertion allel was associated with an increased risk of ESCC compared with the deletion allel of BRM 1321( OR = 1. 35,95% CI = 1. 07- 1. 71). Conclusions: The polymorphism in BRM-1321 is associated with ESCC susceptibility,but no significant association is observed between the polymorphism in BRM-741 and ESCC incidence in Chinese Han population.
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