In vivo evidence of complete circumvention of vincristine resistance by a new triazinoaminopiperidine derivative S 9788 in P388/VCR leukemia model

Cancer Chemother Pharmacol. 1992;30(6):491-4. doi: 10.1007/BF00685604.

Abstract

S 9788, a new triazinoaminopiperidine derivative, was found to be a potent reversant of vincristine resistance in the in vivo murine leukemic P388/VCR model. In two treatment regimens (Q4D days 1, 5 and 9 and QD days 1-9), S 9788 enhanced the antitumor activity of vincristine in a dose-dependent manner, resulting in a complete circumvention of drug resistance for well-tolerated doses of S 9788. S 9788 was also effective in enhancing therapeutic effects of vincristine in the treatment of sensitive P388-bearing mice. These results strongly suggest that S 9788 may be a potential candidate for circumvention of multidrug resistance (MDR) in clinical practice.

MeSH terms

  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Drug Evaluation, Preclinical
  • Drug Resistance / genetics
  • Female
  • Leukemia P388 / drug therapy*
  • Leukemia P388 / genetics
  • Mice
  • Mice, Inbred Strains
  • Piperidines / administration & dosage
  • Piperidines / pharmacology*
  • Triazines / administration & dosage
  • Triazines / pharmacology*
  • Vincristine / administration & dosage
  • Vincristine / therapeutic use*

Substances

  • Piperidines
  • Triazines
  • S 9788
  • Vincristine