首页 | 本学科首页   官方微博 | 高级检索  
     

碱性成纤维细胞生长因子在膀胱移行细胞癌的表达及意义
引用本文:顾晓,眭元庚,徐正铨,吴宏飞,尤国才. 碱性成纤维细胞生长因子在膀胱移行细胞癌的表达及意义[J]. 中国癌症杂志, 2000, 10(1): 39-40,43,I001
作者姓名:顾晓  眭元庚  徐正铨  吴宏飞  尤国才
作者单位:1. 上海市第一人民医院泌尿外科,上海 200080
2. 南京医科大学第一附属医院泌尿外科,江苏,南京,210029
摘    要:目的:研究碱性成纤维细胞生长因子(bFGF)在膀胱移行细胞癌(BTCC)的表达及其意义。方法:应用免疫组化ABC法检测33例BTCC及12例正常膀胱组织中bFGF抗原。结果:bFGF在正常移行细胞呈阴性表达,在正常组织和肿瘤组织的血管内皮细胞、平滑肌细胞均呈弱性表达,肿瘤细胞呈不同程度的阳性表达且过表达率在不同病理分级临床分期间有显著性差异(P〈0.05),在单发与多发、初发与复发组间无显著性差异

关 键 词:膀胱移行细胞癌 bFGF BTCC 基因表达
文章编号:1007-3639(2000)01-0039-02

Expression of basic fibrobalst growth factor in human transitional cell carcinoma of bladder and its significance
GU Xiao,SUI Yun geng,XU Zheng quan,et al.. Expression of basic fibrobalst growth factor in human transitional cell carcinoma of bladder and its significance[J]. China Oncology, 2000, 10(1): 39-40,43,I001
Authors:GU Xiao  SUI Yun geng  XU Zheng quan  et al.
Abstract:Purpose:To evaluate the expression of basic fibroblast growth factor (bFGF) in human transitional cell carcinoma of bladder (BTCC) and its significance. Methods:The expression of bFGF was detected by standard ABC immunohistochemical technique in 33 paraffin embedded tissue specimens of BTCC. Results:All normal transitional cells were negatively stained. Neoplastic cells,smooth muscle cells and endothelial cells of vessels in normal and neoplastic tissue were positively stained. Fisher accurate analysis showed that moderately or strongly positive expression of bFGF in tumor cells closely correlated with different pathological grades ( P <0 05) and clinical stages ( P <0 05). But there was no significant correlation between bFGF over expression and number of lesions ( P <0 05) or postoperative reccurance ( P >0 05). Conclusions:The over expression of bFGF closely correlates with biological behaviour of BTCC and plays an important role in the process of invasiveness and metastasis. This marker may be a new target for comprehensive treatment of BTCC.
Keywords:bladder neoplasms  carcinoma  basic fibroblast growth factor
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