高级检索
易龙, 周晓军, 谢海龙, 陈洁宇, 李青, 杨驰, 计艳, 谢峻, 王勇, 侯亚义. MICA基因多态性与胃癌发病风险相关性[J]. 中国公共卫生, 2006, 22(6): 697-699. DOI: 10.11847/zgggws2006-22-06-37
引用本文: 易龙, 周晓军, 谢海龙, 陈洁宇, 李青, 杨驰, 计艳, 谢峻, 王勇, 侯亚义. MICA基因多态性与胃癌发病风险相关性[J]. 中国公共卫生, 2006, 22(6): 697-699. DOI: 10.11847/zgggws2006-22-06-37
YI Long, ZHOU Xiaojun, XIE Hailong, . Association of MICA gene polymorphism and gastric cancer risk[J]. Chinese Journal of Public Health, 2006, 22(6): 697-699. DOI: 10.11847/zgggws2006-22-06-37
Citation: YI Long, ZHOU Xiaojun, XIE Hailong, . Association of MICA gene polymorphism and gastric cancer risk[J]. Chinese Journal of Public Health, 2006, 22(6): 697-699. DOI: 10.11847/zgggws2006-22-06-37

MICA基因多态性与胃癌发病风险相关性

Association of MICA gene polymorphism and gastric cancer risk

  • 摘要:
      目的   探讨正常人群与胃癌患者的人类组织相容性复合体(MHC)Ⅰ类相关基因A(MICA)各等位基因, 特别是等位基因5.1(A5.1)的基因频率和表型频率的差异, 评价胃癌患者中幽门螺杆菌(Hp)感染与MICA各等位基因分布的关系.
      方法   选取100名胃癌患者与220名无血缘关系健康个体对照, 采用特异引物聚合酶链法, 分析MICA基因的多态性分布; 以ureC基因扩增产物确定是否有Hp感染.
      结果   胃癌组MICA的A5.1基因的表型频率和等位基因频率均高于正常人群对照组(P < 0.05);同时, MICAA5.1的表型频率和等位基因频率低于正常人群对照组(P < 0.05).
      结论   有MICAA5.1等位基因的个体可能有更大患胃癌的风险, 而A5等位基因可能是一个保护性因素.

     

    Abstract:
      Objective   To investigate the possible association of MICAgene polymorphism, especially allele and phenotype of allele 5.1(A5.1), with the risk of gastric cancerand evaluate the possible association of HPpositive ornegative with the gene polymorphism.
      Methods   MICApolymorphism was analyzed in 100 gastric cancerpatients and 220 were randomly selected unrelated controls in Jiangsu province, China by usinglocus-specific prime polymerase chain reactions(PCR), followed by electrophoresis of the PCRproducts in denaturing polyacrylamide gels and subsequent detection by silverstaining.HPwas detected by ureCPCR.
      Results   The phenotype frequency of allele A5.1 of MICAin subjects with gastric cancerwas significantly higherthan thatin controls, as was the frequency of allele.Simultaneously, the phenotype frequency of allele A5 of MICAin subjects with gastric cancerwas significantly lowerthan thatin controls, as was the frequency of allele.
      Conclusion   Allele A5.1 in MICAmight conferthe risk of gastric cancer, and allele A5 seems to be one of protective factors against development of gastric cancer.

     

/

返回文章
返回