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In vivo potentiation of cis-diamminedichloroplatinum (II) antitumor activity by pretreatment with sparsomycin.

Abstract
The influence of protein synthesis inhibition by sparsomycin (Sm) on in vivo cisplatin activity has been studied on BALBc X DBA2: F1 mice bearing L1210 leukemia i.p. Sm alone at the dose range from 0.5 to 3.0 mg/kg did not significantly improve animal survival. Sm potentiated cisplatin activity only when given 3 or 6 h prior to cisplatin (P less than 0.001). Sm 0.5-1.5 mg/kg 3 h prior to cisplatin resulted in a significant prolongation of animal survival (P less than 0.001) and 66% cures in each group versus 0% due to cisplatin alone. Sm pretreatment decreased weight loss due to cisplatin suggesting that it probably is able to decrease cisplatin toxicity.
AuthorsZ Zylicz, D J Wagener, H van Rennes, J M Wessels, E van der Kleijn, W J de Grip, H C Ottenheijm, L A van den Broek
JournalCancer letters (Cancer Lett) Vol. 32 Issue 1 Pg. 53-9 (Jul 1986) ISSN: 0304-3835 [Print] Ireland
PMID3742487 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibiotics, Antineoplastic
  • Sparsomycin
  • Cisplatin
Topics
  • Animals
  • Antibiotics, Antineoplastic (administration & dosage)
  • Antineoplastic Combined Chemotherapy Protocols (therapeutic use)
  • Cisplatin (administration & dosage)
  • Drug Synergism
  • Female
  • Leukemia L1210 (drug therapy, mortality)
  • Mice
  • Mice, Inbred Strains
  • Sparsomycin (administration & dosage)

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