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.
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Authors | Z 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 |
Journal | Cancer letters
(Cancer Lett)
Vol. 32
Issue 1
Pg. 53-9
(Jul 1986)
ISSN: 0304-3835 [Print] Ireland |
PMID | 3742487
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibiotics, Antineoplastic
- Sparsomycin
- Cisplatin
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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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