Abstract |
N-Nitroso(2-hydroxypropyl)(2-oxopropyl)amine (HPOP) proved to be a potent carcinogen in Syrian golden hamsters. The compound is an in vivo metabolite of N-nitrosobis(2-hydroxypropyl)amine, N-nitrosobis(2-oxopropyl)amine (BOP), and N-nitroso-2,6-dimethylmorpholine and a postulated proximate pancreatic carcinogen in hamsters. As with BOP, HPOP induced a higher incidence of pancreatic ductular adenocarcinomas than did N-nitrosobis(2-hydroxypropyl)amine and N-nitroso-2,6-dimethylmorpholine, and these neoplasms showed a great tendency for invasion and metastasis. Also, HPOP induced tumors of the forestomach, liver, gallbladder, kidneys, and vagina (as did BOP). However, HPOP [unlike BOP, but like N-nitrosobis(2-hydroxypropyl)amine and N-nitroso-2,6-dimethylmorpholine] led to tumor development in the nasal cavity, larynx, trachea, intestine, Harderian gland, lips, and flank organ. The possible mechanisms of HPOP carcinogenicity are discussed.
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Authors | P Pour, L Wallcave, R Gingell, D Nagel, T Lawson, S Salmasi, S Tines |
Journal | Cancer research
(Cancer Res)
Vol. 39
Issue 10
Pg. 3828-33
(Oct 1979)
ISSN: 0008-5472 [Print] United States |
PMID | 225009
(Publication Type: Comparative Study, Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Carcinogens
- Nitrosamines
- N-nitroso(2-hydroxypropyl)(2-oxopropyl)amine
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Topics |
- Animals
- Biotransformation
- Carcinogens
- Carcinoma, Intraductal, Noninfiltrating
(chemically induced)
- Cricetinae
- Digestive System Neoplasms
(chemically induced)
- Female
- Male
- Mesocricetus
- Neoplasms, Experimental
(chemically induced, pathology)
- Nitrosamines
(metabolism, toxicity)
- Pancreas
(metabolism)
- Pancreatic Neoplasms
(chemically induced)
- Respiratory Tract Neoplasms
(chemically induced)
- Urogenital Neoplasms
(chemically induced)
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