PKC412 (CGP41251) modulates the proliferation and lipopolysaccharide-induced inflammatory responses of RAW 264.7 macrophages

Biochem Biophys Res Commun. 2007 Aug 17;360(1):115-21. doi: 10.1016/j.bbrc.2007.06.009. Epub 2007 Jun 12.

Abstract

PKC412 (CGP41251) is a multitarget protein kinase inhibitor with anti-tumor activities. Here, we investigated the effects of PKC412 on macrophages. PKC412 inhibited the proliferation of murine RAW 264.7 macrophages through induction of G2/M cell cycle arrest and apoptosis. At non-toxic drug concentrations, PKC412 significantly suppressed the lipopolysaccharide (LPS)-induced release of TNF-alpha and nitric oxide, while instead enhancing IL-6 secretion. PKC412 attenuated LPS-induced phosphorylations of MKK4 and JNK, as well as AP-1 DNA binding activities. Furthermore, PKC412 suppressed LPS-induced Akt and GSK-3beta phosphorylations. These results suggest that the anti-proliferative and immunomodulatory effects of PKC412 are, at least in part, mediated through its interference with the MKK4/JNK/AP-1 and/or Akt/GSK-3beta pathways. Since macrophages contribute significantly to the development of both acute and chronic inflammation, PKC412 may have therapeutic potential and applications in treating inflammatory and/or autoimmune diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / immunology
  • Cell Line
  • Cell Proliferation / drug effects
  • Cytokines / immunology*
  • Dose-Response Relationship, Drug
  • Drug Combinations
  • Immunologic Factors / immunology*
  • Lipopolysaccharides / administration & dosage*
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Macrophages / pathology*
  • Mice
  • Staurosporine / administration & dosage
  • Staurosporine / analogs & derivatives*

Substances

  • Cytokines
  • Drug Combinations
  • Immunologic Factors
  • Lipopolysaccharides
  • Staurosporine
  • midostaurin