首页 | 本学科首页   官方微博 | 高级检索  
     

荧光原位杂交技术检测c-erbB-2和p53基因在胃癌中的表达
引用本文:彭文明,麦卫阳,郑秀玲. 荧光原位杂交技术检测c-erbB-2和p53基因在胃癌中的表达[J]. 癌症, 2000, 19(5): 426-428
作者姓名:彭文明  麦卫阳  郑秀玲
作者单位:广州市第二人民医院病理科!广东广州510150,广州市第二人民医院病理科!广东广州510150,广州市第二人民医院病理科!广东广州510150,广州市第二人民医院病理科!广东广州510150,广州市第二人民医院病理科!广东广州510150,广州市第二人民医院病理科!广东广州510150,广州市第二人民
摘    要:目的:探讨胃癌组织中c-erbB-2和P53基因的表达及其意义。方法:应用荧光原位杂交技术对55例有癌及移行区、正常区组织的常规石蜡包埋标本进行检测。结果:c-erbB-2和P53基石 阳性率分别为36.36%和45.45%,移行芡为10.91%和3.64%,正常粘膜区为3.65%和0,三区间差异无有极显著意义(P值均〈0.01)。在肠型和弥温型胃癌中,c-erbB阳性率分别为51.61%和16.

关 键 词:胃肿瘤 荧光原位杂交 p53基因 c-erbB2基因

Detection of c-erbB-2 and p53 gene expression in human gastric carcinoma by fluorescence in situ hybridization
Abstract:Objective:To investigate the expression of c erbB 2 and p53 gene in gastric carcinoma Method:The C erbB 2 and p53 expressions were dedected by in situ hybridization (FISH) for 55 cases of gastric carcinoma tissues, their transitional region tissues and normal tissues of formalin fixed, paraffinembedded sections Results:The positive rate of c erbB 2 and p53 were 36 1%and 45 5%in cancer tissues, 10 91%and 3 64%in transitional regions, 3 64%and 0 in normal regions respectively There were highly significant differences among the three regions (all P< 0 001) In intestinal type and diffuse type gastric carcinoma, the incidences of c erbB 2 were 51 61%and 16 37%, and of p53 were 25 8%and 70 83%respectively,which was significantly different between two types (all P< 0 05) The expression of c erbB 2 and p53 gene were also correlated with the histological grades of the tumors (P< 0 01 or 0 05) The positive of C erbB 2 gene was related to lymph node metastasis of gastric carcinoma (P< 0 05) Conclusions:The amplification of c erbB 2 gene and mutation of p53 are related to genesis type, differentiation and metastasis, and thus the detection of these gene expression might be useful in evaluating the biological behavior of the tumors
Keywords:Gastric neoplasms  Gene  C erbB 2  p53  Fluorescence in situ Hybridization (FISH)
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号