Enhancement of alkylating agent activity in vitro by PD 128763, a potent poly(ADP-ribose) synthetase inhibitor

Int J Radiat Oncol Biol Phys. 1992;22(3):619-21. doi: 10.1016/0360-3016(92)90889-p.

Abstract

The ability of DNA repair inhibitors to potentiate alkylating agent cytotoxicity was explored with PD 128763, a dihydroisoquinolinone known to effectively inhibit poly(ADP-ribose) synthetase. The cytotoxic activity of streptozotocin in L1210 leukemia cells was maximally potentiated (7-fold decrease in IC50) under conditions of 24 hr exposure to PD 128763 following treatment with the alkylating agent for 1 hr. Similar treatment conditions resulted in a much greater effect (36-fold enhancement in activity) for the 2-nitroimidazole RSU 1069. In contrast, 3-aminobenzamide was only weakly effective at enhancing activity of either streptozotocin or RSU 1069 (2-3 fold potentiation). However, PD 128763 was ineffective at potentiating the cytotoxicity of the bifunctional alkylating agents carmustine (BCNU) and lomustine (CCNU). Our results are consistent with a role for (poly-ADP) ribosylation in the repair of monofunctional alkylating agent damage. This study supports further exploration of the combination of PD 128763 and RSU 1069 as a potentially useful chemotherapeutic regimen.

MeSH terms

  • Alkylating Agents / pharmacology*
  • Animals
  • Carmustine / pharmacology
  • Drug Synergism
  • In Vitro Techniques
  • Isoquinolines / pharmacology*
  • Leukemia L1210
  • Misonidazole / analogs & derivatives
  • Misonidazole / pharmacology
  • Poly(ADP-ribose) Polymerase Inhibitors*
  • Streptozocin / pharmacology
  • Tumor Cells, Cultured

Substances

  • Alkylating Agents
  • Isoquinolines
  • Poly(ADP-ribose) Polymerase Inhibitors
  • 3,4-dihydro-5-methyl-1(2H)-isoquinolinone
  • Streptozocin
  • 1-(2-nitro-1-imidazolyl)-3-aziridino-2-propanol
  • Misonidazole
  • Carmustine