XK469, a topo IIbeta inhibitor, induces apoptosis in Waldenstrom's macroglobulinemia through multiple pathways

Int J Oncol. 2003 Dec;23(6):1637-44.

Abstract

We have previously reported that XK469 inhibited topoisomerase (topo) IIbeta, in Waldenstrom's macroglobulinemia cell line (WSU-WM) however the inhibition alone is not sufficient to induce apoptosis. In this study, the apoptotic potential of XK469 and its mechanism in WSU-WM cell line was investigated. Exposure of WSU-WM cells to XK469 caused a decrease in viable cell number in a dose-dependent manner. In addition, XK469 caused the activation of caspase 3 resulting in subsequent cleavage of PARP. These events were preceded by the release of cytochrome c from the mitochondria to the cytosol. Simultaneous exposure of cells to cyclosporin A prevented the release of cytochrome c to cytosol and reduced the loss of viability. XK469 caused the activation of p53 with up-regulation of p53-dependent proteins such as Bax, p21, Gadd 45 and cyclin B1 in association with G2M arrest. The addition of ubiquitin carboxyl terminal hydrolase (UCH-L1) inhibitor (NaBH4) inhibited up-regulation of p53 and p53 related molecules by XK469 and reduced the loss of viability. Pre-incubation with NOK-1, a monoclonal antibody that prevents Fas-Fas ligand interaction and is inhibitory to Fas signaling interfered with XK469 induced activation of caspase 8 and also reduced the loss of viability. Simultaneous exposure of all three inhibitors (cyclosporin A, NaBH4 and NOK-1) abrogated the toxicity of XK469 by 95%. These data define multiple sequences of biochemical events that mediate cell death induced by XK469. Our study suggests a complex mechanistic cascade of XK469-mediated apoptosis that involves Fas signaling pathway, ubiquitination, p53 activation and cytochrome c release.

MeSH terms

  • Apoptosis*
  • Blotting, Western
  • Caspase 3
  • Caspase 8
  • Caspase 9
  • Caspases / metabolism
  • Cell Cycle
  • Cell Line, Tumor
  • Cell Survival
  • Cyclosporine / metabolism
  • Cytochromes c / metabolism
  • Cytosol / metabolism
  • DNA Damage
  • DNA Topoisomerases, Type II
  • DNA-Binding Proteins
  • Densitometry
  • Dose-Response Relationship, Drug
  • Electron Transport Complex IV / metabolism
  • Enzyme Activation
  • Enzyme Inhibitors / pharmacology*
  • Fas Ligand Protein
  • Fluorometry
  • Humans
  • Ligands
  • Membrane Glycoproteins
  • Mitochondria / metabolism
  • Models, Biological
  • Poly(ADP-ribose) Polymerases / metabolism
  • Quinoxalines / pharmacology*
  • Signal Transduction
  • Time Factors
  • Topoisomerase II Inhibitors*
  • Tumor Suppressor Protein p53 / metabolism
  • Up-Regulation
  • Waldenstrom Macroglobulinemia / metabolism*
  • Waldenstrom Macroglobulinemia / pathology

Substances

  • DNA-Binding Proteins
  • Enzyme Inhibitors
  • FASLG protein, human
  • Fas Ligand Protein
  • Ligands
  • Membrane Glycoproteins
  • Quinoxalines
  • Topoisomerase II Inhibitors
  • Tumor Suppressor Protein p53
  • XK 469
  • Cyclosporine
  • Cytochromes c
  • Electron Transport Complex IV
  • Poly(ADP-ribose) Polymerases
  • CASP3 protein, human
  • CASP8 protein, human
  • CASP9 protein, human
  • Caspase 3
  • Caspase 8
  • Caspase 9
  • Caspases
  • DNA Topoisomerases, Type II