Ubiquitin-like protein conjugation and the ubiquitin-proteasome system as drug targets

被引:442
作者
Bedford, Lynn [2 ]
Lowe, James
Dick, Lawrence R. [1 ]
Mayer, R. John [2 ]
Brownell, James E. [1 ]
机构
[1] Millennium Pharmaceut Inc, Cambridge, MA 02139 USA
[2] Univ Nottingham, Sch Biomed Sci, Nottingham NG7 2UH, England
关键词
KAPPA-B ACTIVATION; VHL TUMOR-SUPPRESSOR; CULLIN-RING LIGASES; X-LINKED INHIBITOR; MYCOBACTERIUM-TUBERCULOSIS; NEDD8-ACTIVATING ENZYME; MULTIPLE-MYELOMA; LYS63-LINKED POLYUBIQUITIN; NEURODEGENERATIVE DISEASE; DEUBIQUITINATING ENZYME;
D O I
10.1038/nrd3321
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The ubiquitin-proteasome system (UPS) and ubiquitin-like protein (UBL) conjugation pathways are integral to cellular protein homeostasis. The growing recognition of the fundamental importance of these pathways to normal cell function and in disease has prompted an in-depth search for small-molecule inhibitors that selectively block the function of these pathways. However, our limited understanding of the molecular mechanisms and biological consequences of UBL conjugation is a significant hurdle to identifying drug-like inhibitors of enzyme targets within these pathways. Here, we highlight recent advances in understanding the role of some of these enzymes and how these new insights may be the key to developing novel therapeutics for diseases including immuno-inflammatory disorders, cancer, infectious diseases, cardiovascular disease and neurodegenerative disorders.
引用
收藏
页码:29 / 46
页数:18
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