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.
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Authors | D E Devor, J R Henneman, L K Keefer, D L Logsdon, J M Rice, A J Streeter, J M Ward |
Journal | Cancer letters
(Cancer Lett)
Vol. 56
Issue 1
Pg. 11-5
(Jan 1991)
ISSN: 0304-3835 [Print] Ireland |
PMID | 2004349
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Drug Combinations
- Mutagens
- Polyenes
- diacetylfecapentaene-12
- Vitamin E
- 1-(1-glycero)dodeca-1,3,5,7,9-pentaene
- Tetradecanoylphorbol Acetate
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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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