Bortezomib sensitizes pancreatic cancer cells to endoplasmic reticulum stress-mediated apoptosis

Cancer Res. 2005 Dec 15;65(24):11658-66. doi: 10.1158/0008-5472.CAN-05-2370.

Abstract

Bortezomib (PS-341, Velcade) is a potent and selective inhibitor of the proteasome that is currently under investigation for the treatment of solid malignancies. We have shown previously that bortezomib has activity in pancreatic cancer models and that the drug induces endoplasmic reticulum (ER) stress but also suppresses the unfolded protein response (UPR). Because the UPR is an important cytoprotective mechanism, we hypothesized that bortezomib would sensitize pancreatic cancer cells to ER stress-mediated apoptosis. Here, we show that bortezomib promotes apoptosis triggered by classic ER stress inducers (tunicamycin and thapsigargin) via a c-Jun NH(2)-terminal kinase (JNK)-dependent mechanism. We also show that cisplatin stimulates ER stress and interacts with bortezomib to increase ER dilation, intracellular Ca(2+) levels, and cell death. Importantly, combined therapy with bortezomib plus cisplatin induced JNK activation and apoptosis in orthotopic pancreatic tumors resulting in a reduction in tumor burden. Taken together, our data establish that bortezomib sensitizes pancreatic cancer cells to ER stress-induced apoptosis and show that bortezomib strongly enhances the anticancer activity of cisplatin.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Apoptosis / drug effects*
  • Boronic Acids / administration & dosage
  • Bortezomib
  • Calcium / metabolism*
  • Carcinogens / pharmacology
  • Caspase Inhibitors
  • Caspases / genetics
  • Caspases / metabolism
  • Cell Line, Tumor
  • Cisplatin / administration & dosage
  • Cytochromes c
  • Drug Interactions
  • Endoplasmic Reticulum / drug effects*
  • Endoplasmic Reticulum / metabolism
  • Enzyme Activation / drug effects
  • Humans
  • Immunoblotting
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Pancreatic Neoplasms / drug therapy*
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology
  • Pyrazines / administration & dosage
  • RNA, Small Interfering / pharmacology
  • Thapsigargin / pharmacology
  • Tumor Stem Cell Assay
  • Tunicamycin / pharmacology

Substances

  • Anti-Bacterial Agents
  • Boronic Acids
  • Carcinogens
  • Caspase Inhibitors
  • Pyrazines
  • RNA, Small Interfering
  • Tunicamycin
  • Thapsigargin
  • Bortezomib
  • Cytochromes c
  • JNK Mitogen-Activated Protein Kinases
  • Caspases
  • Cisplatin
  • Calcium