The proteasome inhibitor PS-341 markedly enhances sensitivity of multiple myeloma tumor cells to chemotherapeutic agents

Clin Cancer Res. 2003 Mar;9(3):1136-44.

Abstract

Increased nuclear factor kappaB (NF-kappaB) activity is associated with increased tumor cell survival in multiple myeloma. The function of NF-kappaB is inhibited through binding to its inhibitor, IkappaB. Release of activated NF-kappaB follows proteasome-mediated degradation of IkappaB resulting from phosphorylation of the inhibitor and, finally, conjugation with ubiquitin. We report that myeloma cells have enhanced IkappaBalpha phosphorylation and increased NF-kappaB activity compared with normal hematopoietic cells. The proteasome inhibitor PS-341 blocked nuclear translocation of NF-kappaB, blocked NF-kappaB DNA binding, and demonstrated consistent antitumor activity against chemoresistant and chemosensitive myeloma cells. The sensitivity of chemoresistant myeloma cells to chemotherapeutic agents was markedly increased (100,000-1,000,000-fold) when combined with a noncytotoxic dose of PS-341 without affecting normal hematopoietic cells. Similar effects were observed using a dominant negative super-repressor for IkappaBalpha. Thus, these results suggest that inhibition of NF-kappaB with PS-341 may overcome chemoresistance and allow doses of chemotherapeutic agents to be markedly reduced with antitumor effects without significant toxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Adenoviridae / genetics
  • Antineoplastic Agents / pharmacology
  • Apoptosis
  • Blotting, Western
  • Boronic Acids / pharmacology*
  • Bortezomib
  • Cell Division
  • Cell Nucleus / metabolism
  • Cell Survival
  • Cysteine Endopeptidases
  • Cytosol / metabolism
  • Dose-Response Relationship, Drug
  • Genes, Dominant
  • Humans
  • I-kappa B Proteins / metabolism
  • Melphalan / pharmacology
  • Microscopy, Fluorescence
  • Multienzyme Complexes / antagonists & inhibitors*
  • Multiple Myeloma / metabolism*
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / metabolism
  • Phosphorylation
  • Proteasome Endopeptidase Complex
  • Pyrazines / pharmacology*
  • Tetrazolium Salts / pharmacology
  • Thiazoles / pharmacology
  • Time Factors
  • Transfection
  • Tumor Cells, Cultured
  • Ubiquitin / metabolism

Substances

  • Antineoplastic Agents
  • Boronic Acids
  • I-kappa B Proteins
  • Multienzyme Complexes
  • NF-kappa B
  • NFKBIA protein, human
  • Pyrazines
  • Tetrazolium Salts
  • Thiazoles
  • Ubiquitin
  • NF-KappaB Inhibitor alpha
  • Bortezomib
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex
  • thiazolyl blue
  • Melphalan