Ubiquitin proteasome pathway: implications and advances in cancer therapy

被引:45
作者
Shah, SA [1 ]
Potter, MW [1 ]
Callery, MP [1 ]
机构
[1] Univ Massachusetts, Med Ctr, Dept Surg, Worcester, MA 01655 USA
来源
SURGICAL ONCOLOGY-OXFORD | 2001年 / 10卷 / 1-2期
关键词
NF-kappa B; apoptosis; p53; p27; p21; chemoresistance;
D O I
10.1016/S0960-7404(01)00018-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The degradation of most eukaryotic cells is controlled by the ubiquitin proteasome pathway. This pathway is responsible not only for the degradation of short and long-lived proteins but also tumor suppressors, transcription factors and cell cycle proteins. Altered degradation of these proteins is thought to promote cancer growth and spread. By contrast, inhibition of the,proteasome would lead to cell cycle arrest and ultimately programmed cell death, or apoptosis. A structured review of the published literature examining the role of ubiquitin proteasome inhibition in cancer growth and regulation is provided. Advances in the development of proteasome inhibitors have allowed detailed investigation of this pathway in cancer growth. Relevant in vitro and in vivo studies of proteasome inhibition as pertains to cancer therapy are detailed. The ubiquitin proteasome pathway is critical in the degradation of proteins involved in cell cycle control and tumor growth. Proteasome inhibitors have been shown to arrest or retard cancer progression, by interfering with the ordered, temporal degradation of regulatory molecules. Clinical trials examining the agents have begun. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:43 / 52
页数:10
相关论文
共 103 条
[71]  
Reed JC, 1996, J CELL BIOCHEM, V60, P23, DOI 10.1002/(SICI)1097-4644(19960101)60:1<23::AID-JCB5>3.0.CO
[72]  
2-5
[73]  
Rieber M, 2000, INT J CANCER, V86, P462, DOI 10.1002/(SICI)1097-0215(20000515)86:4<462::AID-IJC3>3.3.CO
[74]  
2-2
[75]   INHIBITORS OF THE PROTEASOME BLOCK THE DEGRADATION OF MOST CELL-PROTEINS AND THE GENERATION OF PEPTIDES PRESENTED ON MHC CLASS-I MOLECULES [J].
ROCK, KL ;
GRAMM, C ;
ROTHSTEIN, L ;
CLARK, K ;
STEIN, R ;
DICK, L ;
HWANG, D ;
GOLDBERG, AL .
CELL, 1994, 78 (05) :761-771
[76]   The ubiquitin-mediated proteolytic pathway as a therapeutic area [J].
Rolfe, M ;
Chiu, MI ;
Pagano, M .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1997, 75 (01) :5-17
[77]  
ROUSST R, NATURE, V381, P328
[78]   Enhancement of radiosensitivity by proteasome inhibition:: Implications for a role of NF-κB [J].
Russo, SM ;
Tepper, JE ;
Baldwin, AS ;
Liu, R ;
Adams, J ;
Elliott, P ;
Cusack, JC .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 50 (01) :183-193
[79]   Involvement of the proteasome in the programmed cell death of NGF-deprived sympathetic neurons [J].
Sadoul, R ;
Fernandez, PA ;
Quiquerez, AL ;
Martinou, I ;
Maki, M ;
Schroter, M ;
Becherer, JD ;
Irmler, M ;
Tschopp, J ;
Martinou, JC .
EMBO JOURNAL, 1996, 15 (15) :3845-3852
[80]   THE B-TYPE CYCLIN KINASE INHIBITOR P40(SIC1) CONTROLS THE G1 TO S TRANSITION IN SACCHAROMYCES-CEREVISIAE [J].
SCHWOB, E ;
BOHM, T ;
MENDENHALL, MD ;
NASMYTH, K .
CELL, 1994, 79 (02) :233-244