Screening trial with the coordinated gold compound auranofin using mouse lymphocyte leukemia P388

Cancer Res. 1981 Jan;41(1):94-7.

Abstract

The coordinated gold compound, 2,3,4,6-tetra-O-acetyl-1-thio-beta-D-glucopyranosato-S-triethylphosphine-gold (auranofin) was found to be effective in increasing the life span of C57BL x DBA/2 F1 mice inoculated with the lymphocytic leukemia P388. A number of dose schedules were used, the lowest dose being 6 mg/kg every fourth day and the highest dose being 6.0 mg/kg twice daily for 9 days; the lowest and highest doses produced treated versus control ratios of 140 and 220%, respectively. All treatment groups achieved the minimum treated versus control ratio of 125%. Animal weights remained stable at twice-daily and high-dose-daily regimens. Increased life span and weight changes were both found to correlate with drug concentration and/or dose frequency.

MeSH terms

  • Animals
  • Antineoplastic Agents*
  • Auranofin
  • Aurothioglucose / analogs & derivatives*
  • Aurothioglucose / therapeutic use
  • Body Weight / drug effects
  • Drug Evaluation, Preclinical
  • Gold / analogs & derivatives*
  • Leukemia, Experimental / drug therapy*
  • Leukemia, Lymphoid / drug therapy
  • Mice
  • Phosphines / therapeutic use

Substances

  • Antineoplastic Agents
  • Phosphines
  • Aurothioglucose
  • Auranofin
  • Gold