The Ubiquitin-Proteasome System as a Prospective Molecular Target for Cancer Treatment and Prevention

被引:119
作者
Chen, Di
Dou, Q. Ping [1 ,2 ]
机构
[1] Wayne State Univ, Sch Med, Dept Oncol, Detroit, MI 48202 USA
[2] Wayne State Univ, Sch Med, Dept Pathol, Detroit, MI 48201 USA
关键词
Ubiqitin-proteasome pathway; proteasome inhibitors; anti-cancer drugs; chemotherapy; NF-KAPPA-B; ENDOTHELIAL GROWTH-FACTOR; REFRACTORY MULTIPLE-MYELOMA; ANAPHASE-PROMOTING COMPLEX; PEGYLATED LIPOSOMAL DOXORUBICIN; DEPENDENT PROTEOLYTIC SYSTEM; GREEN TEA POLYPHENOLS; RENAL-CELL CARCINOMA; IN-VIVO; INHIBITOR PS-341;
D O I
10.2174/138920310791824057
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Proteasomes are large multicatalytic proteinase complexes located in the cytosol and the nucleus of eukaryotic cells. The ubiquitin-proteasome system is responsible for the degradation of most intracellular proteins and therefore plays an essential regulatory role in critical cellular processes including cell cycle progression, proliferation, differentiation, angiogenesis and apoptosis. Besides involving in normal cellular functions and homeostasis, the alteration of proteasomal activity contributes to the pathological states of several clinical disorders including inflammation, neurodegeneration and cancer. It has been reported that human cancer cells possess elevated level of proteasome activity and are more sensitive to proteasome inhibitors than normal cells, indicating that the inhibition of the ubiquitin-proteasome system could be used as a novel approach for cancer therapy. In this review we summarize several specific aspects of research for the proteasome complex, including the structure and catalytic activities of the proteasome, properties and mechanisms of action of various proteasome inhibitors, and finally the clinical development of proteasome inhibitors as novel anticancer agents.
引用
收藏
页码:459 / 470
页数:12
相关论文
共 163 条
[1]
Development of the proteasome inhibitor PS-341 [J].
Adams, J .
ONCOLOGIST, 2002, 7 (01) :9-16
[2]
Preclinical and clinical evaluation of proteasome inhibitor PS-341 for the treatment of cancer [J].
Adams, J .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2002, 6 (04) :493-500
[3]
The proteasome: A suitable antineoplastic target [J].
Adams, J .
NATURE REVIEWS CANCER, 2004, 4 (05) :349-360
[4]
The development of proteasome inhibitors as anticancer drugs [J].
Adams, J .
CANCER CELL, 2004, 5 (05) :417-421
[5]
Novel dipeptidyl proteasome inhibitors overcome Bcl-2 protective function and selectively accumulate the cyclin-dependent kinase inhibitor p27 and induce apoptosis in transformed, but not normal, human fibroblasts [J].
An, B ;
Goldfarb, RH ;
Siman, R ;
Dou, QP .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (12) :1062-1075
[6]
Anderson Kenneth C., 2000, Hematology Am Soc Hematol Educ Program, P147
[7]
Tome-1, a trigger of mitotic entry, is degraded during G1 via the APC [J].
Ayad, NG ;
Rankin, S ;
Murakami, M ;
Jebanathirajah, J ;
Gygi, S ;
Kirschner, MW .
CELL, 2003, 113 (01) :101-113
[8]
SKP1 connects cell cycle regulators to the ubiquitin proteolysis machinery through a novel motif, the F-box [J].
Bai, C ;
Sen, P ;
Hofmann, K ;
Ma, L ;
Goebl, M ;
Harper, JW ;
Elledge, SJ .
CELL, 1996, 86 (02) :263-274
[9]
Control of the SCFSkp2-Cks1 ubiquitin ligase by the APC/CCdh1 ubiquitin ligase [J].
Bashir, T ;
Dorrello, NV ;
Amador, V ;
Guardavaccaro, D ;
Pagano, M .
NATURE, 2004, 428 (6979) :190-193
[10]
A phase I/II study of arsenic trioxide/bortezomib/ascorbic acid combination therapy for the treatment of relapsed or refractory multiple myeloma [J].
Berenson, James R. ;
Matous, Jeffrey ;
Swift, Regina A. ;
Mapes, Russell ;
Morrison, Blake ;
Yeh, Howard S. .
CLINICAL CANCER RESEARCH, 2007, 13 (06) :1762-1768