Inhibition of proliferation and CD25 down-regulation by retinoic acid in human adult T cell leukemia cells

Leukemia. 1997 Mar;11(3):401-7. doi: 10.1038/sj.leu.2400593.

Abstract

The effects of retinoic acid (RA) on the cell growth and expression of interleukin-2 (IL-2) receptors (IL-2R alpha/p55, Tac, CD25) by the human T lymphotropic virus type I (HTLV-I)-positive T cell lines, HUT102 and ATL-2 were investigated. Incubation of these cells for 48 h with either 13-cis retinoid acid (13-cis RA) or all-trans retinoic acid (ATRA) resulted in marked inhibition of cell growth, determined by 3H-thymidine incorporation, and in down-regulation of CD25 expression, determined by flow cytometry. Four HUT102 cell clones were established by limiting dilution, and 13-cis RA was shown to inhibit cell growth and CD25 expression in three of these clones (HUT102-M5, -M6 and -M7), but not in the fourth (-M8). RA did not induce growth inhibition or down-regulation of CD25 in the HTLV-I-negative T cell lines (Jurkat and MOLT-4) and in normal lymphocytes that had been stimulated with phytohemagglutinin or phorbol 12-myristate 13-acetate. We have shown that RA markedly inhibited both the cell growth and the expression of CD25 in some HTLV-I-positive T cell clones, but not in normal lymphocytes. These results suggest that RA may be suitable for the treatment of patients with adult T cell leukemia (ATL).

MeSH terms

  • Antigens, Neoplasm / metabolism*
  • Cell Division / drug effects
  • Down-Regulation / drug effects
  • Human T-lymphotropic virus 1
  • Humans
  • Leukemia, T-Cell / drug therapy*
  • Leukemia, T-Cell / metabolism
  • Leukemia, T-Cell / pathology
  • Leukocytes, Mononuclear / drug effects
  • Leukocytes, Mononuclear / immunology
  • Lymphocyte Activation / drug effects
  • Phytohemagglutinins / pharmacology
  • Receptors, Interleukin-2 / metabolism*
  • Stimulation, Chemical
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • Thymidine / metabolism
  • Tretinoin / pharmacology*
  • Tritium
  • Tumor Cells, Cultured

Substances

  • Antigens, Neoplasm
  • Phytohemagglutinins
  • Receptors, Interleukin-2
  • Tritium
  • Tretinoin
  • Thymidine