Treatment with interleukin-3 plus granulocyte-macrophage colony-stimulating factors improves the selectivity of Ara-C in vitro against acute myeloid leukemia blasts

Blood. 1991 Nov 15;78(10):2674-9.

Abstract

Hematopoietic growth factors (HGFs) interleukin-3 (IL-3) and granulocyte-macrophage colony-stimulating factor (GM-CSF) individually have been shown to increase the percentage of acute myeloid leukemia (AML) blasts in S phase and enhance the cytotoxic effects of Ara-C against these blasts in culture. We compared in vitro the effects of a combined treatment with GM-CSF (10 ng/mL) plus IL-3 (10 ng/mL) on the metabolism and cytotoxicity of Ara-C in normal bone marrow mononuclear cells (NBMMC) and AML blasts. NBMMC from six healthy volunteers and AML blasts from 10 patients were incubated for 20 hours with or without IL-3 plus GM-CSF, followed by a concurrent treatment with Ara-C for 4 additional hours. Exposure to the HGFs and Ara-C produced significantly higher intracellular Ara-CTP levels as well as higher Ara-CTP/dCTP pool ratios in AML blasts as compared with NBMMC. Treatment with HGFs resulted in [3H] Ara-C DNA incorporation that was significantly higher in AML blasts versus NBMMC. This selective improvement of Ara-C metabolism in AML blasts was associated with an enhanced Ara-C-mediated leukemia colony-forming unit (CFU) growth inhibition. In contrast, exposure to HGFs resulted in an improved colony growth of normal CFU granulocyte-monocyte and CFU-granulocyte, erythroid, monocyte, megakaryocyte. These in vitro studies indicate that a combined treatment with IL-3 plus GM-CSF may improve the selectivity of Ara-C against AML blasts.

Publication types

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

MeSH terms

  • Acute Disease
  • Arabinofuranosylcytosine Triphosphate / metabolism
  • Blast Crisis / blood
  • Blast Crisis / pathology*
  • Bone Marrow Cells
  • Cells, Cultured
  • Colony-Forming Units Assay
  • Cytarabine / metabolism*
  • Cytarabine / pharmacology*
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology*
  • Humans
  • Interleukin-3 / pharmacology*
  • Kinetics
  • Leukemia, Myeloid / blood
  • Leukemia, Myeloid / pathology*
  • Monocytes / cytology
  • Monocytes / drug effects
  • Recombinant Proteins / pharmacology
  • Reference Values
  • Stem Cells / drug effects
  • Stem Cells / pathology*
  • Tumor Cells, Cultured

Substances

  • Interleukin-3
  • Recombinant Proteins
  • Cytarabine
  • Arabinofuranosylcytosine Triphosphate
  • Granulocyte-Macrophage Colony-Stimulating Factor