Reduction of protein kinase C α (PKC-α) promote apoptosis via down-regulation of Dicer in bladder cancer

J Cell Mol Med. 2015 May;19(5):1085-93. doi: 10.1111/jcmm.12503. Epub 2015 Mar 5.

Abstract

In clinic, we examined the expression of protein kinase C (PKC)-α and Dicer in the samples of bladder cancer patients, and found that the two proteins have a line correlation. Our study confirmed this correlation existing by clearing the decreasing expression of Dicer after the PKC-α knockdown. Treatment of bladder cancer cell lines (T24, 5637) with the PKC-α or Dicer knockdown and the PKC inhibitors (Calphostin C and Gö 6976) can promote the apoptosis. Inhibition of PKC can increase the activities of caspase-3 and PARP, however, decrease the expression of Dicer. And knockdown of the PKC-α or Dicer can also activate the caspase-3 or the PARP. Considering the reduction of PKC-α can induce the Dicer down-regulation, we make the conclusion that the reduction of PKC-α can promote the apoptosis via the down-regulation of Dicer in bladder cancer.

Keywords: Dicer; PKC-α; apoptosis; bladder cancer; caspase-3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects
  • Apoptosis / genetics*
  • Blotting, Western
  • Carbazoles / pharmacology
  • Caspase 3 / metabolism
  • Cell Line, Tumor
  • Down-Regulation*
  • Enzyme Inhibitors / pharmacology
  • Fluorescent Antibody Technique
  • Humans
  • Naphthalenes / pharmacology
  • Poly(ADP-ribose) Polymerases / metabolism
  • Protein Kinase C-alpha / antagonists & inhibitors
  • Protein Kinase C-alpha / genetics*
  • Protein Kinase C-alpha / metabolism
  • RNA Interference*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Ribonuclease III / genetics*
  • Ribonuclease III / metabolism
  • Urinary Bladder Neoplasms / genetics
  • Urinary Bladder Neoplasms / metabolism
  • Urinary Bladder Neoplasms / pathology

Substances

  • Carbazoles
  • Enzyme Inhibitors
  • Naphthalenes
  • Go 6976
  • Poly(ADP-ribose) Polymerases
  • PRKCA protein, human
  • Protein Kinase C-alpha
  • Ribonuclease III
  • Caspase 3
  • calphostin C