Activation of nuclear factor κB (NF-κB) in prostate cancer is mediated by protein kinase C epsilon (PKCepsilon)

J Biol Chem. 2012 Oct 26;287(44):37570-82. doi: 10.1074/jbc.M112.398925. Epub 2012 Sep 6.

Abstract

Protein kinase C ε (PKCε) has emerged as an oncogenic kinase and plays important roles in cell survival, mitogenesis and invasion. PKCε is up-regulated in most epithelial cancers, including prostate, breast, and lung cancer. Here we report that PKCε is an essential mediator of NF-κB activation in prostate cancer cells. A strong correlation exists between PKCε overexpression and NF-κB activation status in prostate cancer cells. Moreover, transgenic overexpression of PKCε in the mouse prostate causes preneoplastic lesions that display significant NF-κB hyperactivation. PKCε RNAi depletion or inhibition in prostate cancer cells diminishes NF-κB translocation to the nucleus with subsequent impairment of both activation of NF-κB transcription and induction of NF-κB responsive genes in response to the proinflammatory cytokine tumor necrosis factor α (TNFα). On the other hand, PKCε overexpression in normal prostate cells enhances activation of the NF-κB pathway. A mechanistic analysis revealed that TNFα activates PKCε via a C1 domain/diacylglycerol-dependent mechanism that involves phosphatidylcholine-phospholipase C. Moreover, PKCε facilitates the assembly of the TNF receptor-I signaling complex to trigger NF-κB activation. Our studies identified a molecular link between PKCε and NF-κB that controls key responses implicated in prostate cancer progression.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Active Transport, Cell Nucleus
  • Animals
  • Cell Line, Tumor
  • Gene Expression Regulation, Neoplastic
  • Genes, Reporter
  • Humans
  • I-kappa B Proteins / metabolism
  • Luciferases, Renilla / biosynthesis
  • Luciferases, Renilla / genetics
  • Male
  • Mice
  • Mice, Transgenic
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / metabolism
  • Prostatic Neoplasms / enzymology*
  • Prostatic Neoplasms / metabolism
  • Protein Binding
  • Protein Kinase C-epsilon / metabolism*
  • Protein Kinase C-epsilon / physiology
  • Receptors, Tumor Necrosis Factor, Type I / metabolism
  • Signal Transduction*
  • Transcription Factor RelA / metabolism*
  • Tumor Necrosis Factor-alpha / physiology
  • Type C Phospholipases / metabolism

Substances

  • I-kappa B Proteins
  • NF-kappa B
  • NFKBIA protein, human
  • Nfkbia protein, mouse
  • RELA protein, human
  • Receptors, Tumor Necrosis Factor, Type I
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • NF-KappaB Inhibitor alpha
  • Luciferases, Renilla
  • Protein Kinase C-epsilon
  • Type C Phospholipases
  • phosphatidylcholine-specific phospholipase C