Source:http://linkedlifedata.com/resource/pubmed/id/10835491
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2000-7-18
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pubmed:abstractText |
The influence of 1'-acetoxychavicol acetate (ACA) during the initiation stage was investigated in the N-nitrosobis(2-oxopropyl)amine (BOP)-initiated hamster tumorigenesis model. Ninety male 5-week-old hamsters were divided into three groups, each consisting of 30 animals, and s.c. injected with 20 mg / kg of BOP twice with a one-week interval. Groups 1 through 3 were fed diet supplemented with ACA at concentrations of 500, 100 and 0 ppm, respectively, for 3 weeks starting one week before the first carcinogen application. At the termination of experimental week 54, the total incidence and multiplicity of cholangiocellular adenomas and carcinomas in group 1 (17.9% and 0.3 < 0.9) were significantly (P < 0.05 and P < 0.01) decreased as compared to the group 3 values (50.0% and 0.7 < 0.8). The ACA treatments also showed a tendency to reduce the development of preneoplastic lesions in the pancreas, a main target organ of BOP, although this was not statistically significant. Our results thus indicate that ACA exerts an inhibitory effect on BOP-induced cholangiocarcinogenesis in hamsters. Taken together with previous findings of inhibited colon, oral and skin carcinogenesis in rats and mice, they suggest that ACA is a candidate chemopreventive agent with a wide spectrum of activity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1'-acetoxychavicol acetate,
http://linkedlifedata.com/resource/pubmed/chemical/Anticarcinogenic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Benzyl Alcohols,
http://linkedlifedata.com/resource/pubmed/chemical/Carcinogens,
http://linkedlifedata.com/resource/pubmed/chemical/Nitrosamines,
http://linkedlifedata.com/resource/pubmed/chemical/Terpenes,
http://linkedlifedata.com/resource/pubmed/chemical/nitrosobis(2-oxopropyl)amine
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0910-5050
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
91
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
477-81
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:10835491-Adenocarcinoma,
pubmed-meshheading:10835491-Adenoma,
pubmed-meshheading:10835491-Animals,
pubmed-meshheading:10835491-Anticarcinogenic Agents,
pubmed-meshheading:10835491-Benzyl Alcohols,
pubmed-meshheading:10835491-Bile Duct Neoplasms,
pubmed-meshheading:10835491-Carcinogens,
pubmed-meshheading:10835491-Carcinoma, Hepatocellular,
pubmed-meshheading:10835491-Cholangiocarcinoma,
pubmed-meshheading:10835491-Cricetinae,
pubmed-meshheading:10835491-Drug Screening Assays, Antitumor,
pubmed-meshheading:10835491-Liver Neoplasms,
pubmed-meshheading:10835491-Male,
pubmed-meshheading:10835491-Mesocricetus,
pubmed-meshheading:10835491-Nitrosamines,
pubmed-meshheading:10835491-Pancreatic Neoplasms,
pubmed-meshheading:10835491-Terpenes
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pubmed:year |
2000
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pubmed:articleTitle |
Inhibitory effects of 1'-acetoxychavicol acetate on N-Nitrosobis(2-oxopropyl)-amine-induced initiation of cholangiocarcinogenesis in Syrian hamsters.
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pubmed:affiliation |
Division of Pathology, National Institute of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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