dATP-mediated inhibition of DNA ligase by 2'-deoxycoformycin in T and B cell leukemia

Leukemia. 1989 Feb;3(2):97-103.

Abstract

2'-Deoxycoformycin (dCF), a potent adenosine deaminase inhibitor, has been reported to display greater toxicity for T than for B lymphoblasts. Since this compound can block DNA replication and since this effect is mediated by the intracellular ATP/dATP balance, its possible effect on DNA ligase was investigated. dCF at relatively low concentrations (1 microM), in association with dATP (100 microM), is a strong inhibitor of DNA ligase in T blasts, whereas it has no significant effect in B blasts at this concentration. The AMP-ligase complex is the target of the observed inhibition because the combined presence of the inhibitor and dATP results in a more stable dAMP-ligase complex. Because of this observation and of the greater adenosine deaminase activity observed in T cells, the dATP mediated dCF inhibition of ligase might be the crucial replication target of T cell toxicity. These observations are discussed in terms of T immunodeficiencies including Graft Versus Host Disease and related syndromes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Coformycin / analogs & derivatives
  • Coformycin / pharmacology*
  • DNA Ligases / antagonists & inhibitors*
  • DNA Ligases / metabolism
  • Deoxyadenine Nucleotides / pharmacology*
  • Humans
  • In Vitro Techniques
  • Leukemia, B-Cell / enzymology*
  • Leukemia, T-Cell / enzymology*
  • Pentostatin
  • Polynucleotide Ligases / antagonists & inhibitors*
  • Ribonucleosides / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Deoxyadenine Nucleotides
  • Ribonucleosides
  • Coformycin
  • Pentostatin
  • Adenosine Triphosphate
  • DNA Ligases
  • Polynucleotide Ligases