The PPAR-γ agonist troglitazone antagonizes survival pathways induced by STAT-3 in recombinant interferon-β treated pancreatic cancer cells

Biotechnol Adv. 2012 Jan-Feb;30(1):169-84. doi: 10.1016/j.biotechadv.2011.08.001. Epub 2011 Aug 17.

Abstract

We have previously shown that cancer cells can protect themselves from apoptosis induced by type I interferons (IFNs) through a ras→MAPK-mediated pathway. In addition, since IFN-mediated signalling components STATs are controlled by PPAR gamma we studied the pharmacological interaction between recombinant IFN-β and the PPAR-γ agonist troglitazone (TGZ). This combination induced a synergistic effect on the growth inhibition of BxPC-3, a pancreatic cancer cell line, through the counteraction of the IFN-β-induced activation of STAT-3, MAPK and AKT and the increase in the binding of both STAT-1 related complexes and PPAR-γ with specific DNA responsive elements. The synergism on cell growth inhibition correlated with a cell cycle arrest in G0/G1 phase, secondary to a long-lasting increase of both p21 and p27 expressions. Blockade of MAPK activation and the effect on p21 and p27 expressions, induced by IFN-β and TGZ combination, were due to the decreased activation of STAT-3 secondary to TGZ. IFN-β alone also increased p21 and p27 expression through STAT-1 phosphorylation and this effect was attenuated by the concomitant activation of IFNbeta-induced STAT-3-activation. The combination induced also an increase in autophagy and a decrease in anti-autophagic bcl-2/beclin-1 complex formation. This effect was mediated by the inactivation of the AKT→mTOR-dependent pathway. To the best of our knowledge this is the first evidence that PPAR-γ activation can counteract STAT-3-dependent escape pathways to IFN-β-induced growth inhibition through cell cycle perturbation and increased autophagic death in pancreatic cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Autophagy / drug effects
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Chromans / administration & dosage
  • Chromans / pharmacology*
  • DNA, Neoplasm / metabolism
  • Drug Synergism
  • Humans
  • Interferon-beta / administration & dosage
  • Interferon-beta / pharmacology*
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • PPAR gamma / agonists*
  • Pancreatic Neoplasms / drug therapy*
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology
  • Protein Binding / drug effects
  • Recombinant Proteins / pharmacology
  • STAT3 Transcription Factor / metabolism*
  • Signal Transduction
  • Thiazolidinediones / administration & dosage
  • Thiazolidinediones / pharmacology*
  • Troglitazone

Substances

  • Chromans
  • DNA, Neoplasm
  • PPAR gamma
  • Recombinant Proteins
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Thiazolidinediones
  • Interferon-beta
  • Mitogen-Activated Protein Kinase Kinases
  • Troglitazone