Resistance to different classes of drugs is associated with impaired apoptosis in childhood acute lymphoblastic leukemia

Blood. 2003 Dec 15;102(13):4541-6. doi: 10.1182/blood-2002-11-3612. Epub 2003 Aug 14.

Abstract

Resistance of leukemic cells to chemotherapeutic agents is associated with an unfavorable outcome in pediatric acute lymphoblastic leukemia (ALL). To investigate the underlying mechanisms of cellular drug resistance, the activation of various apoptotic parameters in leukemic cells from 50 children with ALL was studied after in vitro exposure with 4 important drugs in ALL therapy (prednisolone, vincristine, l-asparaginase, and daunorubicin). Exposure to each drug resulted in early induction of phosphatidylserine (PS) externalization and mitochondrial transmembrane (Deltapsim) depolarization followed by caspase-3 activation and poly(ADP-ribose) polymerase (PARP) inactivation in the majority of patients. For all 4 drugs, a significant inverse correlation was found between cellular drug resistance and (1) the percentage of cells with PS externalization (<.001 < P <.008) and (2) the percentage of cells with Deltapsim depolarization (.002 < P <.02). However, the percentage of cells with caspase-3 activation and the percentage of cells with PARP inactivation showed a significant inverse correlation with cellular resistance for prednisolone (P =.001; P =.001) and l-asparaginase (P =.01; P =.001) only. This suggests that caspase-3 activation and PARP inactivation are not essential for vincristine- and daunorubicin-induced apoptosis. In conclusion, resistance to 4 unrelated drugs is associated with defect(s) upstream or at the level of PS externalization and Deltapsim depolarization. This leads to decreased activation of apoptotic parameters in resistant cases of pediatric ALL.

Publication types

  • Comparative Study

MeSH terms

  • Antineoplastic Agents / classification
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / physiology*
  • Asparaginase / pharmacology
  • Caspase 3
  • Caspases / metabolism
  • Child
  • Daunorubicin / pharmacology
  • Drug Resistance, Multiple / physiology*
  • Drug Resistance, Neoplasm / physiology*
  • Enzyme Activation / drug effects
  • Humans
  • Membrane Lipids / metabolism
  • Mitochondria / drug effects
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Phosphatidylserines / metabolism
  • Poly(ADP-ribose) Polymerases / metabolism
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / metabolism
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology
  • Prednisolone / pharmacology
  • Vincristine / pharmacology

Substances

  • Antineoplastic Agents
  • Membrane Lipids
  • Phosphatidylserines
  • Vincristine
  • Prednisolone
  • Poly(ADP-ribose) Polymerases
  • CASP3 protein, human
  • Caspase 3
  • Caspases
  • Asparaginase
  • Daunorubicin