期刊文献+

单核苷酸多态性与胃癌易感性的相关性研究 被引量:1

Correlation between single nucleotide polymorphisms and susceptibility of gastric cancer
下载PDF
导出
摘要 目的研究单核苷酸多态性与胃癌易感性的相关性。方法选取2009年5月~2012年5月笔者所在医院收治的242例胃癌患者血样(实验组)与344例来自健康人群的正常血样(对照组)。对两组血样EZH2rs734004、rs734005、rs2072407、rs6464926、rs12670401多态性测序,运用组织芯片技术与免疫组化检测240例同一来源胃癌组织与30例正常胃黏膜EZH2蛋白表达。结果检测发现EZH2中rs12670401基因型CC与rs6464926基因型TT在胃癌患者中所占的比例较高,EZH2与rs2072404比例增加会严重影响到胃癌发生率与风险(P=0.007,OR=1.785,95%CI=1.171~2.724;P=0.012,OR=1.720,95%CI=1.121~2.623)。胃癌患者中的EZH2包含的杂合基因型rs2072407TC、rs734004TC、rs734004CG所占比例低于正常血液对照组,差异有统计学意义(P<0.05)。所占比例减少可降低患者胃癌发生的几率与风险(P=0.032,OR=0.712,95%CI=0.520~0.975;P=0.033,OR=0.708,95%CI=0.517~0.971;P=0.035,OR=0.712,95%CI=0.517~0.977)。应用连锁不平衡分析LD进一步对上述观察进行证实。胃癌不同组织学类型与不同临床参数间的EZH2免疫组化染色强度差异无统计学意义(P>0.05)。结论单核甘酸多态性与胃癌易感性相关。 Objective To study correlation between single nucleotide polymorphisms and susceptibility of gastric cancer. Methods 242 patients with gastric cancer samples and 344 cases of normal blood group of our hospital from May 2009 to May 2012 were selected. EZH2 rs734004, rs734005, rs2072407, rs6464926, rs12670401 of two groups were polymorphism DNA sequenced. EZH2 protein expression of 240 cases of the same source of gastric carcinoma and 30 cases of normal gastric were detected using tissue microarray technique and immunohistochemical technique. Results The rs12670401genotype CC and rs6464926 genotype TT of EZH2 in patients with gastric cancer in proportion were higher. The increase of EZH2 and rs2072404 in proportion can affect the probability and risk of gastric cancer(P=0.007,OR=1.785,95% CI=1.171-2.724. P=0.012,OR=1.720,95% CI=1.121-2.623). In the patients with gastric cancer, EZH2 contained heterozygous genotypes rs2072407TC, rs734004TC, rs734004CG,which was lower than that of the normal blood group. The difference has statistical significance. The proportion of patients with gastric reduction may reduce the probability and risk (P=0.032, OR=0.712, 95%CI=0.520-0.975.P=0.033,0R=0.708,95%CI=0.517-0.971.P=0.035,OR=0.712,95%CI=0.517-0.977).LD of linkage disequilibrium analysis was used to prove the further official. Immunohistochemical staining intensity of EZH2 of gastric cancer of different histological types and different clinical parameters had no significant difference. Conclusion Single nucleotide polymorphisms and susceptibility of gastric cancer were related.
出处 《中国医药科学》 2012年第17期20-21,共2页 China Medicine And Pharmacy
关键词 胃癌 单核苷酸多态性 遗传易感性 Gastric cancer Single nucleotide polymorphism Genetic predisposition
  • 相关文献

参考文献5

二级参考文献61

  • 1李锦毅,郑华川,杨琳,徐蕾,杨雪飞,高红,张荫昌,辛彦.胃癌中PTEN异常表达与围基因微卫星的杂合性缺失[J].中华肿瘤杂志,2004,26(7):389-392. 被引量:32
  • 2顾学文,陈月香,田秀春,崔飞,朱长仁.PTEN抑癌基因在人胃癌组织中的表达及意义[J].肿瘤研究与临床,2005,17(1):18-20. 被引量:8
  • 3刘茗露,刘斌,邢传平,陈一伟.胃癌组织中KAI1、nm23及P53的表达及其临床意义[J].世界华人消化杂志,2006,14(5):491-496. 被引量:10
  • 4徐飚,王建明.胃癌流行病学研究[J].中华肿瘤防治杂志,2006,13(1). 被引量:159
  • 5王贵吉,邢鑫,倪晨智,裴迎新,王相英,李冰.大肠癌组织中Caveolin-1和EGFR蛋白的表达[J].郑州大学学报(医学版),2007,42(2):308-310. 被引量:5
  • 6Butler MG, Dasouki MJ, Zhou XP, et al. Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations[J].J Med Genet, 2005, 42 (4).- 318-321.
  • 7Oki E, Nakamura T, Tokunaga E, et al. Genetic mutual relationship between PTEN and p53 in gastric cancer [J]. Cancer Lett, 2005, 227 (1): 33-38.
  • 8Hosgood HD, Menashe I, Shen M, et al. Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway [J]. Carcinogenesis, 2008, 29 (10): 1938-1943.
  • 9Rajaraman P, Wang SS, Rothman N, et al. Polymorphisms in apoptosis and cell cycle control genes and risk of brain tumors in adults [J]. Cancer Epidemiol Biomarkers Prev, 2007, 16 (8): 1655-1661.
  • 10Zhou XP, Marsh DJ, Morrison CD, et al. Germline inactivation of PTEN and dysregulation of the phosphoinositol- 3-kinase/Akt pathway cause human Lhermitte-Ductos disease in adults [J]. Am J Hum Genet, 2003, 73 (5): 1191-1198.

共引文献13

同被引文献13

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部