The effects of high dose methylprednisolone on apoptosis in children with acute lymphoblastic leukemia

Clin Lab Haematol. 2003 Feb;25(1):35-40. doi: 10.1046/j.1365-2257.2003.00475.x.

Abstract

Rapid leukemic cell kill at initial diagnosis of patients with acute lymphoblastic leukemia (ALL) has been shown to be associated with a favorable outcome. The aim of the present study was to investigate the effect of high dose methylprednisolone (HDMP) on in vivo blast cell apoptosis in children with ALL. Annexin V-binding and Fas (CD95), Fas ligand (FasL; CD95L), and Bcl-2 expression in PB blasts were determined in newly diagnosed children with ALL before and 4, 24, 96 h after initiation of HDMP treatment (n=20) or conventional dose steroids (CDS) (n=10) as the control group. A decrease in absolute blast count (from 40.8 x 09 to 21.4 x 109/l) associated with an increase in apoptosis (14.2 to 26.9%) (P < 0.05) was detected 4 h after initiation of HDMP. A significant increase in Fas and FasL expression was detected 96 h after HDMP. There was no significant change in apoptosis, Fas and FasL expression from baseline in the control group treated with CDS. The changes in Bcl-2 expression after treatment was not significant in both groups. The results of this preliminary study have shown that HDMP treatment was effective in inducing immediate (within 4 h) blast cell apoptosis. The contribution of Fas/FasL interaction in the rapid component of cell kill remains to be determined, as the increase in the expression of these molecules was evident later.

MeSH terms

  • Apoptosis / drug effects*
  • Child
  • Dose-Response Relationship, Drug
  • Drug Evaluation
  • Fas Ligand Protein
  • Flow Cytometry
  • Gene Expression Regulation
  • Humans
  • Membrane Glycoproteins / analysis
  • Membrane Glycoproteins / biosynthesis
  • Methylprednisolone / pharmacology*
  • Methylprednisolone / therapeutic use
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology
  • Proto-Oncogene Proteins c-bcl-2 / drug effects
  • fas Receptor / analysis
  • fas Receptor / biosynthesis

Substances

  • FASLG protein, human
  • Fas Ligand Protein
  • Membrane Glycoproteins
  • Proto-Oncogene Proteins c-bcl-2
  • fas Receptor
  • Methylprednisolone