Induction of erythroid differentiation in K562 cells by inhibitors of inosine monophosphate dehydrogenase

Cancer Res. 1989 Oct 15;49(20):5555-60.

Abstract

The effects of three inhibitors of inosine monophosphate (IMP) dehydrogenase on a human erythroleukemic cell line, K562, were studied. Following incubation with these inhibitors, K562 cells underwent differentiation and accumulated hemoglobins. The induction of hemoglobin accumulation was dose dependent; maximum induction was observed at 100, 25, and 3 microM, respectively, for ribavirin, tiazofurin, and mycophenolic acid. The induction was associated with reduction of intracellular GTP content and was blocked by adding guanosine within 24 h after adding inducer. The effective dose for half-maximum induction by ribavirin was 3 times less than that for 50% inhibition of K562 proliferation; however, for tiazofurin and mycophenolic acid, it closely approximated the concentrations which suppressed cellular proliferation. Ribavirin was sequestered preferentially inside the K562 cells, and the induction by ribavirin had a greater than 30-fold increase in hemoglobin. Studies with isoelectric focusing, globin chain analyses, and immunochemical assays indicated that both A gamma and G gamma were detected and that the hemoglobin produced in the ribavirin-treated cells consisted of approximately 60% fetal hemoglobin and its acetylated equivalents. The adult-type alpha globin was found, while no beta globin chains were demonstrated. Thus, accumulation of fetal hemoglobin and production of alpha globin chain in ribavirin-treated cells are different from the pattern of hemoglobins induced by hemin.

Publication types

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

MeSH terms

  • Cell Compartmentation
  • Cell Division / drug effects
  • Erythropoiesis / drug effects*
  • Hemoglobins / metabolism
  • Humans
  • IMP Dehydrogenase / antagonists & inhibitors*
  • In Vitro Techniques
  • Ketone Oxidoreductases / antagonists & inhibitors*
  • Leukemia, Erythroblastic, Acute
  • Mycophenolic Acid / pharmacology*
  • Purine Nucleotides / metabolism
  • Ribavirin / analogs & derivatives
  • Ribavirin / metabolism
  • Ribavirin / pharmacology*
  • Ribonucleosides / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Hemoglobins
  • Purine Nucleotides
  • Ribonucleosides
  • Ribavirin
  • IMP Dehydrogenase
  • Ketone Oxidoreductases
  • Mycophenolic Acid
  • tiazofurin