Pharmacodynamics of cytarabine alone and in combination with 7-hydroxystaurosporine (UCN-01) in AML blasts in vitro and during a clinical trial

Blood. 2006 Mar 15;107(6):2517-24. doi: 10.1182/blood-2005-08-3351. Epub 2005 Nov 17.

Abstract

Chk1 and Akt signaling facilitate survival of cells treated with nucleoside analogues. Activation of Chk1 in response to cytarabine (ara-C) induced an S-phase checkpoint characterized by the inhibition of Cdk2, cell cycle arrest, no change in constitutively active Akt, or low-stress kinase signaling in ML-1 cells. However, inhibition of Chk1 by UCN-01 in S-phase-arrested cells resulted in an abrogation of the checkpoint, inhibition of Akt, activation of JNK, and a rapid induction of apoptosis. Similarly, primary acute myelogenous leukemia (AML) blasts exposed to ara-C and UCN-01 demonstrated a selective loss in cloning potential when compared with normal progenitors. Therefore, we evaluated a pilot clinical trial of ara-C in combination with UCN-01 in patients with relapsed AML. Blasts from some patients demonstrated a previously activated Chk1-Cdk2 DNA damage response pathway that decreased during therapy. Constitutively phosphorylated Akt kinase declined on addition of UCN-01 to the ara-C infusion, an action accompanied by an activation of JNK and reduction in absolute AML blast counts. Thus, use of UCN-01 in combination with ara-C decreases Chk1 phosphorylation, inhibits the Akt survival pathway, and activates JNK during the course of therapy, offering a rationale for the cytotoxic action of this combination during AML treatment.

Publication types

  • Clinical Trial
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Apoptosis / drug effects
  • Blast Crisis / drug therapy*
  • Blast Crisis / pathology
  • Cell Cycle / drug effects
  • Checkpoint Kinase 1
  • Cyclin-Dependent Kinase 2 / antagonists & inhibitors
  • Cytarabine / administration & dosage
  • Cytarabine / pharmacokinetics*
  • DNA Damage
  • Humans
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Leukemia, Myeloid, Acute / drug therapy*
  • Leukemia, Myeloid, Acute / pathology
  • Middle Aged
  • Oncogene Protein v-akt / antagonists & inhibitors
  • Oncogene Protein v-akt / metabolism
  • Pharmacokinetics
  • Phosphorylation
  • Pilot Projects
  • Protein Kinases / metabolism
  • Salvage Therapy / methods
  • Staurosporine / administration & dosage
  • Staurosporine / analogs & derivatives*
  • Staurosporine / pharmacokinetics
  • Tumor Cells, Cultured

Substances

  • Cytarabine
  • 7-hydroxystaurosporine
  • Protein Kinases
  • CHEK1 protein, human
  • Checkpoint Kinase 1
  • Oncogene Protein v-akt
  • CDK2 protein, human
  • Cyclin-Dependent Kinase 2
  • JNK Mitogen-Activated Protein Kinases
  • Staurosporine