Phosphorylation of p53, induction of Bax and activation of caspases during beta-lapachone-mediated apoptosis in human prostate epithelial cells

Int J Oncol. 2002 Dec;21(6):1293-9.

Abstract

The DNA topoisomerase I inhibitor beta-lapachone, the product of a tree from South America, is known to exhibit various biological properties, the mechanisms of which are poorly understood. We investigated the effects of beta-lapachone on the growth of human prostate epithelial cells. Upon treatment with beta-lapachone, a concentration-dependent inhibition of cell viability was observed and cells developed many of the hallmark features of apoptosis, including condensation of chromatin and DNA fragmentation. The apoptotic effects of beta-lapachone were associated with marked induction of p53 phosphorylation and Bax protein without altering the expression of p53 and Bcl-2 protein. In addition, the proteolytic cleavage of specific target proteins such as poly(ADP-ribose) polymerase, beta-catenin and Rad51, which are hallmarks of apoptosis, were observed, and Western blotting demonstrated that processing/activation of caspases release cytochrome c from the mitochondria into the cytosol and accompany the generation of beta-lapachone-mediating apoptotic cell death. However, beta-lapachone did not affect the levels of c-IAP family proteins. The present results suggest that apoptotic signals evoked by beta-lapachone in human prostate epithelial cells may converge caspases activation through up-regulation of phosphorylation of p53 and Bax rather than down-regulation of c-IAPs family.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibiotics, Antineoplastic / pharmacology*
  • Apoptosis / drug effects*
  • Blotting, Western
  • Caspases / metabolism*
  • Cytochrome c Group / metabolism
  • Cytoskeletal Proteins / metabolism
  • DNA-Binding Proteins / metabolism
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Humans
  • Inhibitor of Apoptosis Proteins
  • Male
  • Naphthoquinones / pharmacology*
  • Phosphorylation
  • Poly(ADP-ribose) Polymerases / metabolism
  • Prostate / metabolism
  • Prostate / pathology*
  • Proteins / metabolism
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Rad51 Recombinase
  • Topoisomerase I Inhibitors
  • Trans-Activators / metabolism
  • Tumor Suppressor Protein p53 / metabolism*
  • Up-Regulation
  • bcl-2-Associated X Protein
  • beta Catenin

Substances

  • Antibiotics, Antineoplastic
  • BAX protein, human
  • CTNNB1 protein, human
  • Cytochrome c Group
  • Cytoskeletal Proteins
  • DNA-Binding Proteins
  • Inhibitor of Apoptosis Proteins
  • Naphthoquinones
  • Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Topoisomerase I Inhibitors
  • Trans-Activators
  • Tumor Suppressor Protein p53
  • bcl-2-Associated X Protein
  • beta Catenin
  • beta-lapachone
  • Poly(ADP-ribose) Polymerases
  • RAD51 protein, human
  • Rad51 Recombinase
  • Caspases