期刊文献+

食管癌前病变和癌组织中p15、p16、mdm2和p53蛋白的表达 被引量:8

Expression of p15,p16,mdm2,and p53 protein in different precancerous lesion and esophageal carcinoma tissue
下载PDF
导出
摘要 目的:探讨食管癌高发区河南林州市食管癌患者p15、p16、mdm2和p53的表达变化特征及其与各级病变的关系。方法:取食管癌高发区河南林州市居民156例的食管内镜黏膜活检组织(包括正常食管上皮(NOR)21例,基底细胞过度增生(BCH)45例,不典型增生(DYS)23例,原位癌组织(CIS)45例和鳞状细胞癌(SCC)22例),采用免疫组化ABC法分析p15、p16、mdm2和p53蛋白的表达情况。结果:NOR和各级癌前病变组织及SCC组织中均出现不同程度的p15、p16、mdm2和p53表达。随着病变发展(从NOR→BCH→DYS→CIS→SCC),p15和p16的表达逐渐降低,mdm2和p53的表达逐渐增高(P<0.05)。结论:p15、p16的低表达和p53、mdm2的高表达可能是导致病变持续向癌方向发生发展的机制之一。 Aim: To characterize the changes of P15, p16, mdm2 and p53 expression in esophageal normal epithelial tissue and different precancerous lesions and esophageal carcinoma. Mothods: A total of 156 esophageal biopsy samples, including 21 cases of normal esophageal epithelia (NOR) ,45 cases of basal cell hyperplasia (BCH) , 22 cases of dysplasia (DYS) , 45 cases of carcinoma in situ (CIS) , and 22 cases of esophageal squamous cell carcinoma (SCC) , were subjected to determine the expression of p15, p16, mdm2 and p53 using immunohistochemical ABC method. Results: With the lesions progressed from NOR→BCH→DYS→CIS→SCC, the positive rates of p15 and p16 decreased ( P 〈 0.05) , and the positive rates of mdm2 and p53 increased significantly( P 〈 0.05 ). Conclusion: The low-expression of P15, p16 and high- expression of mdm2 and p53 may be one of the mechanisms to drive the mild lesions towards carcinogenesis.
出处 《郑州大学学报(医学版)》 CAS 北大核心 2006年第1期47-48,共2页 Journal of Zhengzhou University(Medical Sciences)
基金 国家杰出青年科学基金资助项目30025016 河南省高校创新人才工程基金资助项目1999125 河南省医学科技攻关基金资助项目20058 河南省食管癌重点开放实验室基金资助项目20050227 郑州大学211工程基金资助项目
关键词 食管肿瘤 癌前病变 P15 P16 MDM2 P53 esophageal neoplasm precancerous lesion carcinoma p15 p16 mdm2 p53
  • 相关文献

参考文献7

  • 1王立东,郑树.河南食管癌高发区人群食管和贲门癌变机制[J].郑州大学学报(医学版),2002,37(6):717-729. 被引量:100
  • 2Xing EP,Nie Y,Song Y,et al.Mechanisms of inactivation of p14ARF,p15INK4b,and p16INK4a genes in haman esophageal squamous cell carcinoma.Clin Cancer Res,1999,5(10):2704.
  • 3Gombart AF,Morosetti R,Miller CW,et al.Deletions of the cyclin-dependent kanase inhibitor genes p16INK4A and p15INK4B in non-Hodgkin's lymphomas.Blood,1995,86(4):1534.
  • 4Quelle DE,Zindy F,Ashmun RA,et al.Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest.Ce11,1995,83(6):993.
  • 5Price BD,Park SJ.DNA damage increases the levels of MDM2 messenger RNA in wtp53 human cell.Cancer Res,1994,54(4):896.
  • 6Freedman DA,Wu L,Levine AJ.Functions of the MDM2oncoprotein.Cell Mol Life Sci,1999,55(1):96.
  • 7Zhang RW,Wang H.MDM2 oncogene as a novel target for human cancer therapy.Curr Pharm Des,2000,6 (4):393.

二级参考文献14

共引文献99

同被引文献91

引证文献8

二级引证文献18

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