Downregulation of Bid is associated with PKCepsilon-mediated TRAIL resistance

Cell Death Differ. 2007 Apr;14(4):851-60. doi: 10.1038/sj.cdd.4402077. Epub 2006 Dec 22.

Abstract

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a promising anticancer agent as it selectively kills tumor cells but spares normal cells. Resistance to TRAIL by tumor cells limits its therapeutic use. We have previously shown that protein kinase C-epsilon (PKCepsilon) acts as an antiapoptotic protein in MCF-7 breast cancer cells. In the present study, we have investigated the mechanism(s) by which PKCepsilon contributes to TRAIL resistance. Overexpression of PKCepsilon inhibited caspase-8 and -9 activation, release of mitochondrial cytochrome c and cell death induced by TRAIL, but did not interfere with the recruitment of caspase-8 to the death-inducing signaling complex. Knockdown/inhibition of PKCepsilon resulted in enhanced sensitivity to TRAIL. The level of Bcl-2 was increased and Bid was decreased by PKCepsilon at both the protein and mRNA level but PKCepsilon had no effect on Bax. Knockdown of Bcl-2 by siRNA reversed TRAIL resistance in PKCepsilon-overexpressing cells, whereas depletion of Bid contributed to TRAIL resistance in MCF-7 cells. A decrease in Bid content was also associated with inhibition of TRAIL-induced caspase-8 activation. Furthermore, PKCepsilon depletion or overexpression of DN-PKCepsilon was associated with a decrease in Bcl-2 protein level. Thus, our results suggest that PKCepsilon acts upstream of mitochondria and mediates TRAIL resistance via both Bcl-2 and Bid in MCF-7 cells.

Publication types

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

MeSH terms

  • Apoptosis / physiology*
  • BH3 Interacting Domain Death Agonist Protein / genetics
  • BH3 Interacting Domain Death Agonist Protein / metabolism*
  • Breast Neoplasms / metabolism
  • Caspases / metabolism
  • Cell Line, Tumor
  • Down-Regulation / genetics
  • Female
  • Flow Cytometry
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Protein Kinase C-epsilon / genetics
  • Protein Kinase C-epsilon / metabolism*
  • RNA, Small Interfering / genetics
  • TNF-Related Apoptosis-Inducing Ligand / metabolism*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • BH3 Interacting Domain Death Agonist Protein
  • Intracellular Signaling Peptides and Proteins
  • RNA, Small Interfering
  • TNF-Related Apoptosis-Inducing Ligand
  • Protein Kinase C-epsilon
  • Caspases