Cited by 85Ubiquitin and proteasome pathwaysProtease and Inhibitor MechanismsProtein Degradation and Inhibitors

Clinical development of novel proteasome inhibitors for cancer treatment

Open access
Yang, Huanjie, Zonder, Jeffrey A, Dou, Q Ping·2009·Expert Opinion on Investigational Drugs

Abstract

BACKGROUND: Emerging evidence demonstrates that targeting the tumor proteasome is a promising strategy for cancer therapy. OBJECTIVE: This review summarizes recent results from cancer clinical trials using specific proteasome inhibitors or some natural compounds that have proteasome-inhibitory effects. METHODS: A literature search was carried out using PubMed. Results about the clinical application of specific proteasome inhibitors and natural products with proteasome-inhibitory activity for cancer prevention or therapy were reviewed. RESULTS/CONCLUSION: Bortezomib, the reversible proteasome inhibitor that first entered clinical trials, has been studied extensively as a single agent and in combination with glucocorticoids, cytotoxic agents, immunomodulatory drugs and radiation as treatment for multiple myeloma and other hematological malignancies. The results in some cases have been impressive. There is less evidence of bortezomib's efficacy in solid tumors. Novel irreversible proteasome inhibitors, NPI-0052 and carfilzomib, have also been developed and clinical trials are underway. Natural products with proteasome-inhibitory effects, such as green tea polyphenol (-)-epigallocatechin-3-gallate (EGCG), soy isoflavone genistein, and the spice turmeric compound curcumin, have been studied alone and in combination with traditional chemotherapy and radiotherapy against various cancers. There is also interest in developing these natural compounds as potential chemopreventive agents.

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Authors
Yang, H., Zonder, J. A., & Dou, Q. P.
Affiliations
Wayne State University (US)
Venue
Expert Opinion on Investigational Drugs
Published
2009-06-08
Volume
18
Issue
7
Pages
957-971
ISSN
  • 1354-3784 (ISSN-L)
  • 1744-7658
OpenAlex
W2036211695
Cited by
85
References
2
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FWCI
0.89
Type
journal article
Language
en
Open access
Locations
  • Expert Opinion on Investigational Drugs (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Cancer Institute (R03CA112625, R01CA120009, P30CA022453)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Protease and Inhibitor Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Degradation and Inhibitors
Keywords
proteasome inhibitors, bortezomib, carfilzomib, NPI-0052, multiple myeloma, hematologic malignancies, solid tumors, natural products, epigallocatechin gallate, genistein, curcumin, chemoprevention, combination therapy, clinical trials
MeSH terms
Animals, Antineoplastic Agents, Clinical Trials as Topic, Humans, Neoplasms, Treatment Outcome, Proteasome Endopeptidase Complex, Drug Discovery, Proteasome Inhibitors

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

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