Effect of a new de-N-acetyl-lysoglycosphingolipid on some tumour models.

Abstract

A new de-N-acetylated glycosphingolipid termed WILD20, a breakdown product of GM1 obtained through alkaline hydrolysis, and characterized by nuclear magnetic resonance, mass spectrometry and elementary analysis, was found to inhibit phospholipase A2 via phosphokinase C translocation blockade. The substance inhibited various tumour cell lines in vitro, in synergy with doxorubicin and cisplatin. In vivo, it showed an antitumoral effect when both the tumour cells and WILD20 were injected at the same site (peritoneal cavity). Tumour cells, incubated with WILD20, showed a dose-dependent decrease of oncogenicity without impairment of viability. WILD20 also down-regulated tumour cell adherence to laminin and fibronectin. When peritumorally administered, WILD20 impaired tumour growth and potentiated the peritumoral effects of recombinant interleukin 2. The results obtained merit exploration of the therapeutical possibilities of this agent in human cancer patients.

• Authors: E Tubaro, G P Borelli, L Belogi, G Cavallo, A Santoni, F Mainiero
• Journal: European journal of pharmacology (Eur J Pharmacol) Vol. 294 Issue 2-3 Pg. 555-63 (Dec 29 1995) ISSN: 0014-2999 [Print] Netherlands
• PMID: 8750718 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• Gangliosides
• WILD 20

Topics

• Animals
• Antineoplastic Agents (pharmacology)
• Carbohydrate Sequence
• Cell Division (drug effects)
• Gangliosides (pharmacology)
• Humans
• Male
• Mice
• Mice, Inbred C57BL
• Molecular Sequence Data
• Neoplasms, Experimental (drug therapy)
• Tumor Cells, Cultured