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[辽宁地区MUC1基因多态性与胃癌易感性的关系]

[The relationship between the polymorphism of MUC1 and susceptibility to gastric cancer in Liaoning region].

作者信息

Xu Qian, Sun Li-Ping, Gong Yue-Hua, Xu Ying, Dong Nan-Nan, Yuan Yuan

机构信息

Cancer Control Laboratory of Cancer Institute and General Surgery Institute, the First Affiliated Hospital of China Medical University, Shenyang 110001, China.

出版信息

Yi Chuan. 2008 Sep;30(9):1163-8. doi: 10.3724/sp.j.1005.2008.01163.

Abstract

Analyzed the relationship between 568 site A/G polymorphism in mucin 1(MUC1) gene in a population from Liaoning Province and susceptibility to gastric cancer. Sequence specific primers-polymerase chain reaction(PCR-SSPs) were performed to analyze the genotype of the A/G polymorphism in its 568 site of exon 2 for 138 gastric cancer cases and 131 normal ones tested, and ELISA was performed to test IgG antibody of H. pylori. We found that the distribution frequency of AA, AG, GG three genotypes were 73.3%, 22.1%, 4.6%, respectively. The frequency of AA genotype was statistically higher in the gastric cancer (GC) group compared to the control group(P=0.03), moreover, individuals with the MUC1 AA genotype increased 1.92 fold risk for gastric cancer. And compared with subjects carrying both AG+GG genotype and H. pylori-IgG negative, there was an obviously increased risk of developing gastric cancer for those who carried both AA genotype and H. pylori-IgG negative, both AG+GG genotype and H. pylori-IgG positive, and both AG+GG genotype and H. pylori-IgG negative, but there were no significantly differences between the every two of the latter three. Our results indicated that there was a relationship between MUC1 A/G polymorphism and susceptibility to gastric cancer. And there were probably no statistically interaction between the 568 site A/G polymorphism in MUC1 and H. pylori infection in the occurrence and development process of gastric cancer.

摘要

分析辽宁省某人群中黏蛋白1(MUC1)基因568位点A/G多态性与胃癌易感性之间的关系。采用序列特异性引物-聚合酶链反应(PCR-SSPs)对138例胃癌患者和131例正常对照者进行外显子2第568位点A/G多态性的基因型分析,并用酶联免疫吸附测定法(ELISA)检测幽门螺杆菌IgG抗体。结果发现,AA、AG、GG三种基因型的分布频率分别为73.3%、22.1%、4.6%。与对照组相比,胃癌组AA基因型频率差异有统计学意义(P=0.03),而且MUC1基因AA基因型个体患胃癌的风险增加1.92倍。与携带AG+GG基因型且幽门螺杆菌IgG阴性的个体相比,携带AA基因型且幽门螺杆菌IgG阴性、携带AG+GG基因型且幽门螺杆菌IgG阳性、携带AG+GG基因型且幽门螺杆菌IgG阴性的个体发生胃癌的风险均明显增加,但后三者两两之间差异无统计学意义。结果提示,MUC1基因A/G多态性与胃癌易感性有关,且在胃癌发生发展过程中MUC1基因568位点A/G多态性与幽门螺杆菌感染之间可能不存在统计学交互作用。

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