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Inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced tumor promotion and epidermal ornithine decarboxylase activity in mouse skin by palmitoylcarnitine.

Abstract
Palmitoylcarnitine, which has been reported to be an inhibitor of calcium-activated, phospholipid-dependent protein kinase (protein kinase C), inhibited 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced epidermal ornithine decarboxylase in mouse skin in a dose-dependent manner. Neither acetylcarnitine nor palmitic acid inhibited TPA-caused ornithine decarboxylase induction. In addition, palmitoylcarnitine markedly inhibited skin tumor promotion induced by TPA. Palmitoylcarnitine inhibited epidermal protein kinase C activity which was stimulated by Ca2+ in the presence of phosphatidylserine but failed to inhibit the enzyme activity which was stimulated by TPA in the presence of either phosphatidylserine or Ca2+ plus phosphatidylserine. Therefore, it seems unlikely that the potent anti-tumor-promoting action of palmitoylcarnitine, which is shown in the present study, is explained solely by its effect on protein kinase C.
AuthorsT Nakadate, S Yamamoto, E Aizu, R Kato
JournalCancer research (Cancer Res) Vol. 46 Issue 4 Pt 1 Pg. 1589-93 (Apr 1986) ISSN: 0008-5472 [Print] United States
PMID3081251 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Ornithine Decarboxylase Inhibitors
  • Phorbols
  • Palmitoylcarnitine
  • Egtazic Acid
  • Protein Kinase C
  • Ornithine Decarboxylase
  • Tetradecanoylphorbol Acetate
  • Carnitine
  • Calcium
Topics
  • Animals
  • Calcium (pharmacology)
  • Carnitine (analogs & derivatives)
  • Dose-Response Relationship, Drug
  • Egtazic Acid (pharmacology)
  • Female
  • Mice
  • Mice, Inbred Strains
  • Ornithine Decarboxylase (analysis)
  • Ornithine Decarboxylase Inhibitors
  • Palmitoylcarnitine (pharmacology)
  • Phorbols (antagonists & inhibitors)
  • Protein Kinase C (analysis, antagonists & inhibitors)
  • Skin (enzymology)
  • Skin Neoplasms (chemically induced, prevention & control)
  • Tetradecanoylphorbol Acetate (antagonists & inhibitors)
  • Time Factors

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