Augmentation by aphidicolin of 1-beta-D-arabinofuranosylcytosine-induced c-jun and NF-kappa B activation in a human myeloid leukemia cell line: correlation with apoptosis

Leuk Res. 1995 Sep;19(9):645-50. doi: 10.1016/0145-2126(95)00046-q.

Abstract

1-beta-D-arabinofuranosylcytosine (ara-C) (2 microM) can induce apoptosis in a human myeloid leukemia cell line, U937, after 4 h of incubation. Pretreatment of cells with aphidicolin (2 microM) augments ara-C-induced apoptosis, since it was first observed at 0.4 microM ara-C and became more intense at 2 and 10 microM. Although aphidicolin itself had a marginal effect on c-jun expression, it significantly augmented ara-C induced c-jun upregulation by shortening the lag time and lowering ara-C concentrations necessary for the induction of detectable c-jun transcripts. Aphidicolin and ara-C acted synergistically to increase NF-kappa B DNA binding activity as determined by an electrophoretic mobility shift assay. Expression of c-myc was slightly increased through the DNA degradative phase, and was then downregulated. Thus, the activation of NF-kappa B and c-jun expression seems to be well correlated with the potentiation by aphidicolin of ara-C-induced apoptosis.

MeSH terms

  • Antimetabolites, Antineoplastic / administration & dosage*
  • Aphidicolin / administration & dosage*
  • Apoptosis / drug effects*
  • Base Sequence
  • Cytarabine / administration & dosage*
  • DNA Damage / drug effects
  • DNA Polymerase II / antagonists & inhibitors*
  • Drug Synergism
  • Enzyme Inhibitors / administration & dosage*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Genes, jun*
  • Genes, myc
  • Humans
  • Molecular Sequence Data
  • NF-kappa B / genetics*
  • Oligodeoxyribonucleotides / chemistry
  • Proto-Oncogene Proteins c-jun / genetics*
  • RNA, Messenger / genetics
  • Tumor Cells, Cultured

Substances

  • Antimetabolites, Antineoplastic
  • Enzyme Inhibitors
  • NF-kappa B
  • Oligodeoxyribonucleotides
  • Proto-Oncogene Proteins c-jun
  • RNA, Messenger
  • Cytarabine
  • Aphidicolin
  • DNA Polymerase II