Abstract |
An oral tumor model has been developed in inbred Syrian golden hamsters by continuous applications every 2 weeks of methyl(acetoxymethyl)nitrosamine [( DMN-OAC) CAS: 56856-83-8; methylnitrosaminomethyl ester acetic acid] at 2 mg/kg body weight alone or by a single application of DMN-OAC followed by continuous twice weekly applications of 12-O-tetradecanoylphorbol 13-acetate (TPA) (1 microgram/animal). Similar studies were done in the W rat buccal mucosa. In the hamsters treated continuously with DMN-OAC, 100% of the tumors were observed in the cheek pouch; none were observed at other sites. In contrast, in the rats treated similarly, only a 67% tumor incidence was observed, of which only 42% were oral tumors. A promoter effect of TPA was observed in hamster cheek pouch tumors induced by DMN-OAC, whereas rat oral mucosa did not respond to TPA treatment.
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Authors | S V Bhide, K M Munir, M Wiessler, A V Sarode, C S Soman |
Journal | Journal of the National Cancer Institute
(J Natl Cancer Inst)
Vol. 73
Issue 3
Pg. 737-41
(Sep 1984)
ISSN: 0027-8874 [Print] United States |
PMID | 6590918
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Carcinogens
- methyl(acetoxymethyl)nitrosamine
- Dimethylnitrosamine
- Tetradecanoylphorbol Acetate
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Topics |
- Animals
- Carcinogens
- Cheek
- Cricetinae
- Dimethylnitrosamine
(analogs & derivatives, toxicity)
- Mouth Mucosa
(drug effects, pathology)
- Mouth Neoplasms
(chemically induced, pathology)
- Rats
- Tetradecanoylphorbol Acetate
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