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Carcinogenicity study of fecapentaene-12 diacetate on skin painting in SENCAR mice.

Abstract
To investigate the effects of both diol esterification and coadministration with antioxidant on the tumorigenicity of fecapentaene-12 (FP-12) preparations, diacetylfecapentaene-12 (DAFP-12) in dimethylsulfoxide (DMSO) was applied to SENCAR mouse skin with or without the stabilizer, vitamin E, twice/week for 5 weeks, following which all animals were promoted for up to 25 weeks by weekly applications of 12-O-tetradecanoylphorbol-13-acetate (TPA). While positive controls receiving 7,12-dimethylbenz[a]anthracene (DMBA) instead of DAFP-12 in a similar protocol all developed papillomas (average of 23/animal), papilloma incidence in mice given DAFP-12 did not differ significantly from that of the vehicle control. We conclude that DAFP-12 shows little or no tumor initiating activity for mouse skin even when coadministered with vitamin E.
AuthorsD E Devor, J R Henneman, L K Keefer, D L Logsdon, J M Rice, A J Streeter, J M Ward
JournalCancer letters (Cancer Lett) Vol. 56 Issue 1 Pg. 11-5 (Jan 1991) ISSN: 0304-3835 [Print] Ireland
PMID2004349 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Drug Combinations
  • Mutagens
  • Polyenes
  • diacetylfecapentaene-12
  • Vitamin E
  • 1-(1-glycero)dodeca-1,3,5,7,9-pentaene
  • Tetradecanoylphorbol Acetate
Topics
  • Adult
  • Animals
  • Drug Combinations
  • Female
  • Humans
  • Mice
  • Mutagens (pharmacology)
  • Papilloma (chemically induced)
  • Polyenes (adverse effects, pharmacology)
  • Skin Neoplasms (chemically induced)
  • Tetradecanoylphorbol Acetate (pharmacology)
  • Vitamin E (pharmacology)

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