Inhibition of phosphatidylinositol 3-kinase causes apoptosis in retinoic acid differentiated hl-60 leukemia cells

Cell Cycle. 2004 Jan;3(1):67-70.

Abstract

Phosphatidylinositol 3-kinase (PI3-K) signaling may inhibit apoptosis in neoplastic cells. The PI-3K inhibitor wortmannin renders cells apoptosis-prone. Inducers of differentiation may also cause apoptosis. To detect the effect of wortmannin on the survival of differentiated human acute promyeloid leukemia cells, HL-60 cells were induced to differentiation with treatment of all trans-retinoic acid (ATRA) followed by treatment with wortmannin. Results showed that apoptosis occurred in cells that underwent differentiation, but not in undifferentiated HL-60 cells. The pro-apoptotic molecule, Bad, played a role in this apoptotic mechanism. Thus, the survival of differentiated HL-60 cells induced by ATRA depends on the ability of the PI3-K pathway to transduce survival signals; the PI3-K inhibitor, wortmannin, can induce apoptosis of differentiated HL-60 cells. These results may indicate a novel method for treating cancer with differentiation induction and signal pathway regulation.

MeSH terms

  • Androstadienes / pharmacology
  • Antineoplastic Agents / pharmacology
  • Apoptosis / physiology*
  • Carrier Proteins / metabolism
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology*
  • DNA Fragmentation / physiology
  • Enzyme Inhibitors / pharmacology*
  • HL-60 Cells
  • Humans
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphoinositide-3 Kinase Inhibitors
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Signal Transduction / physiology
  • Tretinoin / pharmacology
  • Wortmannin
  • bcl-Associated Death Protein

Substances

  • Androstadienes
  • Antineoplastic Agents
  • BAD protein, human
  • Carrier Proteins
  • Enzyme Inhibitors
  • Phosphoinositide-3 Kinase Inhibitors
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-Associated Death Protein
  • Tretinoin
  • Wortmannin