S-Phase-specific activation of PKC alpha induces senescence in non-small cell lung cancer cells

J Biol Chem. 2008 Feb 29;283(9):5466-76. doi: 10.1074/jbc.M707576200. Epub 2007 Dec 26.

Abstract

Protein kinase C (PKC) has been widely implicated in positive and negative control of cell proliferation. We have recently shown that treatment of non-small cell lung cancer (NSCLC) cells with phorbol 12-myristate 13-acetate (PMA) during G1 phase inhibits the progression into S phase, an effect mediated by PKC delta-induced up-regulation of the cell cycle inhibitor p21 Cip1. However, PMA treatment in asynchronously growing NSCLC cells leads to accumulation of cells in G2/M. Studies in post-G1 phases revealed that PMA induced an irreversible G2/M cell cycle arrest in NSCLC cells and conferred morphological and biochemical features of senescence, including elevated SA-beta-Gal activity and reduced telomerase activity. Remarkably, this effect was phase-specific, as it occurred only when PKC was activated in S, but not in G1, phase. Mechanistic analysis revealed a crucial role for the classical PKC alpha isozyme as mediator of the G2/M arrest and senescence, as well as for inducing p21(Cip1) an obligatory event for conferring the senescence phenotype. In addition to the unappreciated role of PKC isozymes, and specifically PKC alpha, in senescence, our data introduce the paradigm that discrete PKCs trigger distinctive responses when activated in different phases of the cell cycle via a common mechanism that involves p21 Cip1 up-regulation.

Publication types

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

MeSH terms

  • Carcinogens / pharmacology
  • Carcinoma, Non-Small-Cell Lung / enzymology*
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cellular Senescence* / drug effects
  • Cellular Senescence* / genetics
  • Cyclin-Dependent Kinase Inhibitor p21 / biosynthesis*
  • Cyclin-Dependent Kinase Inhibitor p21 / genetics
  • Enzyme Activation / drug effects
  • Enzyme Activation / genetics
  • Gene Expression Regulation, Neoplastic / drug effects
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Protein Kinase C-alpha / genetics
  • Protein Kinase C-alpha / metabolism*
  • Protein Kinase C-delta / genetics
  • Protein Kinase C-delta / metabolism*
  • S Phase* / drug effects
  • S Phase* / genetics
  • Telomerase / genetics
  • Telomerase / metabolism
  • Tetradecanoylphorbol Acetate / pharmacology
  • Up-Regulation / drug effects
  • Up-Regulation / genetics
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism

Substances

  • CDKN1A protein, human
  • Carcinogens
  • Cyclin-Dependent Kinase Inhibitor p21
  • Isoenzymes
  • Protein Kinase C-alpha
  • Protein Kinase C-delta
  • Telomerase
  • beta-Galactosidase
  • Tetradecanoylphorbol Acetate