Clinical and Marketed Proteasome Inhibitors for Cancer Treatment

Jiankang Zhang, Peng Wu, Yongzhou Hu

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

The ubiquitin-proteasome pathway (UPP), which influences essential cellular functions including cell growth, differentiation, apoptosis, signal transduction, antigen processing and inflammatory responses, has been considered as one of the most important cellular protein degradation approaches. Proteasome functions as a gatekeeper, which controls the execution of protein degradation and plays a critical role in the ubiquitin-proteasome pathway. The unfolding of the close connection between proteasome and cancer provides a potential strategy for cancer treatment by using proteasome inhibitors. Small molecular inhibitors of varied structures and potency against proteasome have been discovered in recent years, with bortezomib and carfilzomib having been successfully approved for clinical application while some other promising candidates are currently under clinical trials. Herein, we review the development history of drugs and candidates that target the 20S proteasome, structure-activity relationships (SARs) of various proteasome inhibitors, and related completed or ongoing clinical trials.
Original languageEnglish
JournalCurrent Medicinal Chemistry
Volume20
Issue number20
Pages (from-to)2537-2551
Number of pages15
ISSN0929-8673
DOIs
Publication statusPublished - 2013
Externally publishedYes

Keywords

  • Molecular Medicine
  • Pharmacology
  • Cancer
  • Clinical development
  • Marketed
  • Proteasome
  • Proteasome inhibitor
  • SAR
  • Benzyloxycarbonylleucylleucylleucinal
  • Bortezomib
  • Carfilzomib
  • Delanzomib
  • Ixazomib
  • Oprozomib
  • Salinosporamide A
  • Anemia
  • Cancer chemotherapy
  • Drug efficacy
  • Drug marketing
  • Drug mechanism
  • Drug safety
  • enzyme activity
  • Hematologic malignancy
  • Mantle cell lymphoma
  • Multiple myeloma
  • Neoplasm
  • Neutropenia
  • Nonhuman
  • Pneumonia
  • Protein function
  • protein structure
  • Solid tumor
  • structure activity relation
  • thrombocytopenia
  • Boron Compounds
  • Boronic Acids
  • Glycine
  • Humans
  • Lactones
  • Neoplasms
  • Oligopeptides
  • Proteasome Endopeptidase Complex
  • Proteasome Inhibitors
  • Pyrazines
  • Pyrroles
  • Structure-Activity Relationship
  • Threonine
  • Biochemistry
  • Chemistry
  • NF-KAPPA-B
  • ADVANCED SOLID TUMORS
  • MULTICATALYTIC PROTEINASE COMPLEX
  • DOXORUBICIN PLUS BORTEZOMIB
  • CELL-CYCLE REGULATION
  • Phase-I trial
  • 20S Proteasome
  • Open-label
  • Cancer Neoplasms (MeSH) neoplastic disease drug therapy
  • 20S proteasome 140879-24-9
  • Proteasome inhibitors antineoplastic-drug, enzyme inhibitor-drug clinical trial
  • ubiquitin-proteasome signaling, inhibition
  • 12512, Pathology - Therapy
  • 22002, Pharmacology - General
  • 24004, Neoplasms - Pathology, clinical aspects and systemic effects
  • 24008, Neoplasms - Therapeutic agents and therapy
  • Structure-activity relationship analysis mathematical and computer techniques
  • Tumor Biology
  • MLN 9708
  • ONX 0912
  • Marizomib
  • 2ZD004190S Threonine
  • 6IF28942WO delanzomib
  • EC 3.4.25.1 Proteasome Endopeptidase Complex
  • TE7660XO1C Glycine

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