p53-dependent expression of PIG3 during proliferation, genotoxic stress, and reversible growth arrest

Cancer Lett. 2000 Aug 1;156(1):63-72. doi: 10.1016/s0304-3835(00)00441-9.

Abstract

The p53-inducible gene 3 (PIG3) was recently identified in a screen for genes induced by p53 before the onset of apoptosis. PIG3 shares significant homology with oxidoreductases from several species. In this study, PIG3-specific antibodies were used to analyze cellular PIG3 protein levels under control and genotoxic stress conditions. PIG3 protein was localized to the cytoplasm and induced in primary, non-transformed, and transformed cell cultures after exposure to genotoxic agents. The induction of PIG3 was p53-dependent and occurred with delayed kinetics as compared with other p53 downstream targets, such as p21 and MDM2. Using a p53-inducible cell model system, in which p53-mediated growth arrest is reversible, we found that PIG3 levels were increased during p53-mediated growth arrest. Interestingly, elevated levels of PIG3 were maintained in cells that resumed cycling in the absence of ectopic p53 expression, suggesting that PIG3 is a long-lived reporter, which may be useful for detecting transient activation of p53.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Apoptosis
  • Cell Cycle
  • Cell Division
  • Colonic Neoplasms / drug therapy
  • Colonic Neoplasms / pathology
  • Colonic Neoplasms / radiotherapy
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / genetics
  • Doxorubicin / pharmacology
  • Gene Expression Regulation
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins*
  • Proteins / physiology*
  • Proto-Oncogene Proteins / physiology
  • Proto-Oncogene Proteins c-mdm2
  • Tumor Cells, Cultured
  • Tumor Suppressor Protein p53 / analysis
  • Tumor Suppressor Protein p53 / physiology*

Substances

  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • Proteins
  • Proto-Oncogene Proteins
  • TP53I3 protein, human
  • Tumor Suppressor Protein p53
  • Doxorubicin
  • MDM2 protein, human
  • Proto-Oncogene Proteins c-mdm2