Pharmacological targets in the ubiquitin system offer new ways of treating cancer, neurodegenerative disorders and infectious diseases

被引:81
作者
Edelmann, Mariola J. [2 ]
Nicholson, Benjamin [3 ]
Kessler, Benedikt M. [1 ]
机构
[1] Univ Oxford, Nuffield Dept Med, Oxford OX3 7BN, England
[2] Mississippi State Univ, Inst Gen Biocomp & Biotechnol, Mississippi Agr & Forestry Expt Stn, Mississippi State, MS 39762 USA
[3] Progenra Inc, Malvern, PA 19355 USA
来源
EXPERT REVIEWS IN MOLECULAR MEDICINE | 2011年 / 13卷
关键词
ACTIVATING ENZYME-INHIBITOR; SMALL-MOLECULE INHIBITORS; MANTLE CELL LYMPHOMA; RESPIRATORY SYNDROME CORONAVIRUS; MARINE-DERIVED FUNGUS; PAPAIN-LIKE PROTEASE; NF-KAPPA-B; DEUBIQUITINATING ENZYMES; IN-VIVO; NEDD8-ACTIVATING ENZYME;
D O I
10.1017/S1462399411002031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent advances in the development and discovery of pharmacological interventions within the ubiquitin-proteasome system (UPS) have uncovered an enormous potential for possible novel treatments of neurodegenerative disease, cancer, immunological disorder and microbial infection. Interference with proteasome activity, although initially considered unlikely to be exploitable clinically, has already proved to be very effective against haematological malignancies, and more specific derivatives that target subsets of proteasomes are emerging. Recent small-molecule screens have revealed inhibitors against ubiquitin-conjugating and -deconjugating enzymes, many of which have been evaluated for their potential use as therapeutics, either as single agents or in synergy with other drugs. Here, we discuss recent advances in the characterisation of novel UPS modulators (in particular, inhibitors of ubiquitin-conjugating and -deconjugating enzymes) and how they pave the way towards new therapeutic approaches for the treatment of proteotoxic disease, cancer and microbial infection.
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页数:17
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