Bryostatin 1 and UCN-01 potentiate 1-beta-D-arabinofuranosylcytosine-induced apoptosis in human myeloid leukemia cells through disparate mechanisms

Mol Pharmacol. 2003 Jan;63(1):232-42. doi: 10.1124/mol.63.1.232.

Abstract

The effects of the PKC activator and down-regulator bryostatin 1 and the PKC and Chk1 inhibitor 7-hydroxystaurosporine (UCN-01) were compared with respect to potentiation of 1-beta-D-arabinofuranosylcytosine (ara-C)-induced apoptosis in human myelomonocytic leukemia cells (U937). Whereas bryostatin 1 and UCN-01 both markedly enhanced ara-C-induced mitochondrial injury (e.g., cytochrome c and Smac/DIABLO release, loss of mitochondrial membrane potential), caspase activation, and apoptosis, ectopic expression of an N-terminal loop-deleted Bcl-2 mutant protein protected cells from ara-C/UCN-01- but not ara-C/bryostatin 1-mediated lethality. Conversely, ectopic expression of CrmA or dominant-negative caspase-8 abrogated potentiation of ara-C-mediated apoptosis by bryostatin 1 but not by UCN-01. Exposure of cells to ara-C and bryostatin 1 (but not UCN-01) resulted in sustained release of tumor necrosis factor (TNF) alpha; moreover, potentiation of ara-C lethality by bryostatin 1 (but not by UCN-01) was reversed by coadministration of TNF soluble receptors or the selective PKC inhibitor bisindolylmaleimide (1 microM). Finally, similar events were observed in the human promyelocytic leukemia cell line HL-60. Together, these findings suggest that potentiation of ara-C lethality in human myeloid leukemia cells by bryostatin 1 but not UCN-01 involves activation of the extrinsic, receptor-mediated apoptotic pathway, and represents a consequence of bryostatin 1-mediated release of TNF-alpha. They also argue that the mechanism by which bryostatin 1 promotes ara-C-induced mitochondrial injury, caspase activation, and apoptosis involves factors other than or in addition to PKC down-regulation or modulation of Bcl-2 phosphorylation status.

Publication types

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

MeSH terms

  • Alkaloids / pharmacology*
  • Antineoplastic Agents / pharmacology*
  • Apoptosis Regulatory Proteins
  • Apoptosis*
  • Bryostatins
  • Carrier Proteins / metabolism
  • Caspases / metabolism
  • Cytarabine / pharmacology*
  • Cytochrome c Group / metabolism
  • Drug Synergism
  • Enzyme Activation / drug effects
  • Gene Deletion
  • HL-60 Cells
  • Humans
  • Indoles
  • Intracellular Signaling Peptides and Proteins
  • Lactones / pharmacology*
  • Leukemia, Myeloid / pathology*
  • Macrolides
  • Maleimides
  • Mitochondrial Proteins / metabolism
  • Mutation
  • Phosphorylation
  • Protein Kinase C / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Receptors, Tumor Necrosis Factor / metabolism
  • Staurosporine / analogs & derivatives
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / metabolism
  • U937 Cells

Substances

  • Alkaloids
  • Antineoplastic Agents
  • Apoptosis Regulatory Proteins
  • Bryostatins
  • Carrier Proteins
  • Cytochrome c Group
  • DIABLO protein, human
  • Indoles
  • Intracellular Signaling Peptides and Proteins
  • Lactones
  • Macrolides
  • Maleimides
  • Mitochondrial Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factor-alpha
  • Cytarabine
  • bryostatin 1
  • 7-hydroxystaurosporine
  • Protein Kinase C
  • Caspases
  • Staurosporine
  • bisindolylmaleimide I