Clinical update: proteasome inhibitors in solid tumors

Cancer Treat Rev. 2003 May;29 Suppl 1:41-8. doi: 10.1016/s0305-7372(03)00082-3.

Abstract

The proteasome plays a critical role in regulating the cell cycle, neoplastic growth, and metastasis. Bortezomib (VELCADE; formerly PS-341, LDP-341, MLN341) is a novel dipeptide boronic acid that is the first proteasome inhibitor to have progressed to clinical trials. Preclinical research has shown that through the prevention of IkappaB degradation, bortezomib may block chemotherapy-induced NF-kappaB activation and augment the apoptotic response to chemotherapeutic agents. Bortezomib also appeared to increase the stabilization of p21 and p27, as well as transcription factor p53. In preclinical models of breast, lung, pancreatic, and ovarian tumor types, bortezomib inhibited tumor growth and demonstrated anti-angiogenic properties. Bortezomib exhibited the greatest activity when combined with standard chemotherapeutic agents, such as irinotecan, gemcitabine, and docetaxel, suggesting its potential additive/syngeristic role in overcoming resistance to conventional chemotherapy. Preliminary data from early clinical trials suggest that bortezomib can be given at pharmacologically active doses in combination with standard doses of chemotherapy with manageable toxicities. Responses have been seen and no evidence of additive toxicity has been exhibited in combination agent trials.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Apoptosis / drug effects
  • Boronic Acids / pharmacology*
  • Bortezomib
  • Clinical Trials, Phase I as Topic
  • Clinical Trials, Phase II as Topic
  • Cysteine Endopeptidases / pharmacology*
  • Drug Interactions
  • Humans
  • Microfilament Proteins / biosynthesis
  • Multienzyme Complexes / antagonists & inhibitors*
  • Multienzyme Complexes / pharmacology*
  • Muscle Proteins*
  • NF-kappa B / pharmacology
  • Neoplasms / drug therapy*
  • Protease Inhibitors / pharmacology*
  • Proteasome Endopeptidase Complex
  • Pyrazines / pharmacology*
  • Tumor Suppressor Protein p53 / biosynthesis

Substances

  • Boronic Acids
  • Microfilament Proteins
  • Multienzyme Complexes
  • Muscle Proteins
  • NF-kappa B
  • Protease Inhibitors
  • Pyrazines
  • Tagln protein, mouse
  • Tumor Suppressor Protein p53
  • Bortezomib
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex