首页 | 本学科首页   官方微博 | 高级检索  
     

肿瘤坏死因子相关凋亡诱导配体的凋亡诱导机制及其药物开发
引用本文:肿瘤坏死因子相关凋亡诱导配体的凋亡诱导机制及其药物开发[J]. 中国药科大学学报, 2004, (4): 91-94.
作者姓名:刘洪波  范学工  李宁
作者单位:中南大学湘雅医院,长沙,410008
摘    要:肿瘤坏死因子相关凋亡诱导配体(TRAIL)是TNF超家族成员,它与死亡受体(death receptor,DR)结合,启动细胞内信号途径,特异性诱导肿瘤细胞等凋亡,一般不对机体正常组织产生毒性效应,可望成为新型抗肿瘤药物.然而TRAIL可能的肝细胞毒性严重阻碍其临床应用.本文就TRAIL诱导凋亡的机制及其TRAIL药物开发的前景作一综述.

关 键 词:肿瘤坏死因子相关凋亡诱导配体  凋亡  肿瘤  肝细胞毒性  药物开发
文章编号:1000-5048(2004)04-0381-04
修稿时间:2003-11-10

Mechanism of TNF Related Apoptosis Inducing Ligand Inducing Apoptosis and Its Pharmaceutical Exploitation
Mechanism of TNF Related Apoptosis Inducing Ligand Inducing Apoptosis and Its Pharmaceutical Exploitation[J]. Journal of China Pharmaceutical University, 2004, (4): 91-94.
Authors:LIU Hong-Bo  FAN Xue-Gong  LI Ling
Abstract:TNF related apoptosis inducing ligand(TRAIL) belongs to TNF(tumor necrosis factor) superfamily. It's binding to death receptor (DR) initiate cellular signaling,and specially induces the apoptosis in tumor cells but not in normal tissue cells. So TRAIL seems to be a promising agent,but the possible hepatocyte toxicity of TRAIL severely impedes its clinical use. This paper reviews the mechanism of TRAIL inducing apoptosis and the prospect of TRAIL pharmaceutical exploitation.
Keywords:TRAIL  Apoptosis  Tumor  Hepatotoxic  Pharmaceutical exploitation
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《中国药科大学学报》浏览原始摘要信息
点击此处可从《中国药科大学学报》下载全文
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