Recombinant human interferon sensitizes resistant myeloid leukemic cells to induction of terminal differentiation

Biochem Biophys Res Commun. 1985 Jul 16;130(1):379-88. doi: 10.1016/0006-291x(85)90428-0.

Abstract

Recombinant human leukocyte interferon (IFN-alpha A) inhibits growth of the human promyelocytic leukemic cell line HL-60 without inducing these cells to differentiate terminally. When IFN-alpha A is combined with agents capable of inducing differentiation in HL-60 cells, such as 12-O-tetradecanoyl-phorbol-13-acetate (TPA), cis or trans retinoic acid (RA) or dimethylsulfoxide (DMSO), growth suppression and induction of differentiation are dramatically increased. By growing HL-60 cells in increasing concentrations of TPA, RA, or DMSO, a series of sublines have been developed which are resistant to the usual growth inhibition and induction of differentiation seen when wild type HL-60 cells are exposed to these agents. Treatment of these resistant HL-60 cells with the combination of IFN-alpha A and the appropriate inducer results, however, in a synergistic suppression in cell growth and a concomitant induction of terminal differentiation. The ability of interferon to interact synergistically with agents which promote leukemic cell maturation may represents a novel means of reducing resistant leukemic cell populations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation / drug effects*
  • Cell Division / drug effects
  • Cell Line
  • Dimethyl Sulfoxide / pharmacology
  • Drug Synergism
  • Humans
  • Interferon Type I / pharmacology*
  • Leukemia, Myeloid, Acute / pathology*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Tretinoin / pharmacology

Substances

  • Interferon Type I
  • Tretinoin
  • Tetradecanoylphorbol Acetate
  • Dimethyl Sulfoxide