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Discovering proteasomal deubiquitinating enzyme inhibitors for cancer therapy: lessons from rational design, nature and old drug reposition
- Publication Year :
- 2018
- Publisher :
- Future Science Ltd, 2018.
-
Abstract
- The ubiquitin proteasome system has been validated as a target of cancer therapies evident by the US FDA approval of anticancer 20S proteasome inhibitors. Deubiquitinating enzymes (DUBs), an essential component of the ubiquitin proteasome system, regulate cellular processes through the removal of ubiquitin from ubiquitinated-tagged proteins. The deubiquitination process has been linked with cancer and other pathologies. As such, the study of proteasomal DUBs and their inhibitors has garnered interest as a novel strategy to improve current cancer therapies, especially for cancers resistant to 20S proteasome inhibitors. This article reviews proteasomal DUB inhibitors in the context of: discovery through rational design approach, discovery from searching natural products and discovery from repurposing old drugs, and offers a future perspective.
- Subjects :
- 0301 basic medicine
Proteasome Endopeptidase Complex
Context (language use)
Antineoplastic Agents
Review
Deubiquitinating enzyme
03 medical and health sciences
0302 clinical medicine
Ubiquitin
Neoplasms
Drug Discovery
Medicine
Animals
Humans
Repurposing
Pharmacology
biology
Deubiquitinating Enzymes
business.industry
Rational design
Drug Repositioning
Ubiquitination
Cancer
medicine.disease
030104 developmental biology
Proteasome
030220 oncology & carcinogenesis
Drug Design
biology.protein
Cancer research
Molecular Medicine
business
Proteasome Inhibitors
Deubiquitination
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....1536ad0cf8c804b550f564598be994d2