Effects of the proteasome inhibitor PS-341 on apoptosis and angiogenesis in orthotopic human pancreatic tumor xenografts

Mol Cancer Ther. 2002 Dec;1(14):1243-53.

Abstract

Recent studies have shown that the transcription factor, nuclear factor kappaB (NF-kappaB), regulates critical survival pathways in a variety of different cell types, including human pancreatic cancer cells. The activation of NF-kappaB is controlled by proteasome-mediated degradation of its endogenous polypeptide inhibitor, inhibitor of nuclear factor kappaBalpha. We investigated the effects of PS-341, a peptide boronate inhibitor of the proteasome in human pancreatic cancer cells in vitro and in vivo. Comparison of PS-341's effects on the growth of eight different human pancreatic cancer cell lines revealed marked heterogeneity in drug responsiveness, ranging from highly resistant (IC50 > 10 microM; Panc-48, HS766T, and Mia-PaCa-2) to extremely sensitive (IC50 < 40 nM; L3.6pl, Hpaf2, and BxPC3). However, these effects did not correlate with differential inhibition of NF-kappaB activation. Direct quantification of apoptosis revealed that PS-341's effects on cell growth largely correlated with sensitivity to programmed cell death. Evaluation of PS-341's effects on established orthotopic tumor xenografts demonstrated that biweekly intravenous administration of the maximum-tolerated dose of the drug (1 mg/kg) led to significant reductions in the volumes of L3.6pl tumors but not Mia-PaCa-2 tumors. Laser scanning cytometer-mediated quantification of drug-induced apoptosis in the xenografts confirmed that PS-341 induced DNA fragmentation and activation of caspase-3 in L3.6pl tumors but not in Mia-PaCa-2 tumors. However, histological examination of drug-treated tumors revealed extensive central necrosis and reductions in microvessel density and VEGF expression in both tumor types. Taken together, our results demonstrate that PS-341 inhibits the growth of human pancreatic tumors via direct effects on tumor cells and indirect effects on the tumor vasculature.

MeSH terms

  • Animals
  • Apoptosis*
  • Caspases / metabolism
  • Cell Division
  • Cell Survival
  • Cysteine Endopeptidases / metabolism
  • DNA Fragmentation
  • Dose-Response Relationship, Drug
  • Endothelial Growth Factors / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • I-kappa B Proteins / metabolism
  • Immunoblotting
  • Immunohistochemistry
  • Inhibitory Concentration 50
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Lymphokines / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Multienzyme Complexes / antagonists & inhibitors*
  • Multienzyme Complexes / metabolism
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / metabolism
  • Neoplasm Transplantation
  • Neovascularization, Pathologic*
  • Pancreatic Neoplasms / blood supply
  • Pancreatic Neoplasms / drug therapy*
  • Pancreatic Neoplasms / pathology
  • Protease Inhibitors / pharmacology
  • Proteasome Endopeptidase Complex
  • Time Factors
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors

Substances

  • Endothelial Growth Factors
  • I-kappa B Proteins
  • Intercellular Signaling Peptides and Proteins
  • Lymphokines
  • Multienzyme Complexes
  • NF-kappa B
  • NFKBIA protein, human
  • Nfkbia protein, mouse
  • Protease Inhibitors
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • NF-KappaB Inhibitor alpha
  • Caspases
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex