hPNAS-4 inhibits proliferation through S phase arrest and apoptosis: underlying action mechanism in ovarian cancer cells

Apoptosis. 2013 Apr;18(4):467-79. doi: 10.1007/s10495-012-0797-z.

Abstract

PNAS-4, a novel pro-apoptotic gene, was activated during the early response to DNA damage. Previous studies have shown that hPNAS-4 can inhibit tumor growth when over-expressed in ovarian cancer cells. However, the underlying action mechanism remains elusive. In this work, we found that hPNAS-4 expression was significantly increased in SKOV3 cells when exposed to cisplatin, methyl methanesulfonate or mitomycin C, and that its overexpression could induce proliferation inhibition, S phase arrest and apoptosis in A2780s and SKOV3 ovarian cancer cells. The S phase arrest caused by hPNAS-4 was associated with up-regulation of p21. p21 is p53-dispensable and correlates with activation of ERK, and activation of the Cdc25A-Cdk2-Cyclin E/Cyclin A pathway, while the pro-apoptotic effects of hPNAS-4 were mediated by activation of caspase-9 and -3 other than caspase-8, and accompanied by release of AIF, Smac and cytochrome c into the cytosol. Taken together, these data suggest a new mechanism by which hPNAS-4 inhibits proliferation of ovarian cancer cells by inducing S phase arrest and apoptosis via activation of Cdc25A-Cdk2-Cyclin E/Cyclin A axis and mitochondrial dysfunction-mediated caspase-dependent and -independent apoptotic pathways. To our knowledge, we provide the first molecular evidence for the potential application of hPNAS-4 as a novel target in ovarian cancer gene therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis Inducing Factor / metabolism
  • Apoptosis Regulatory Proteins / metabolism*
  • Apoptosis*
  • Carbon-Nitrogen Lyases
  • Caspase 3 / metabolism
  • Caspase 8 / metabolism
  • Caspase 9 / metabolism
  • Cell Line, Tumor
  • Cell Proliferation
  • Cisplatin / pharmacology
  • Cyclin A / metabolism
  • Cyclin E / metabolism
  • Cyclin-Dependent Kinase 2 / metabolism
  • Cyclin-Dependent Kinase Inhibitor p21 / biosynthesis
  • Cytochromes c / metabolism
  • DNA Damage*
  • Enzyme Activation
  • Female
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Methyl Methanesulfonate / pharmacology
  • Mitochondrial Proteins / metabolism
  • Mitomycin / pharmacology
  • Ovarian Neoplasms / metabolism*
  • Ovarian Neoplasms / pathology*
  • S Phase Cell Cycle Checkpoints*
  • Up-Regulation
  • cdc25 Phosphatases / metabolism

Substances

  • AIFM1 protein, human
  • Apoptosis Inducing Factor
  • Apoptosis Regulatory Proteins
  • Cyclin A
  • Cyclin E
  • Cyclin-Dependent Kinase Inhibitor p21
  • DIABLO protein, human
  • Intracellular Signaling Peptides and Proteins
  • Mitochondrial Proteins
  • Mitomycin
  • Cytochromes c
  • Methyl Methanesulfonate
  • CDK2 protein, human
  • Cyclin-Dependent Kinase 2
  • CDC25A protein, human
  • cdc25 Phosphatases
  • Caspase 3
  • Caspase 8
  • Caspase 9
  • Carbon-Nitrogen Lyases
  • DESI2 protein, human
  • Cisplatin