Lack of Inhibition of BBN-induced Bladder Carcinogenesis in C57BL/6 Mice by Intravesical Instillation of KRN 7000
Autor: | Tatsuya Nakatani, Hideki Wanibuchi, Seiji Wada, Kenichiro Doi, Chikayoshi Masuda, Keiichirou Morimura, Min Wei, Shoji Fukushima, Tadao Kakizoe, Makoto Mitsuhashi |
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Rok vydání: | 2003 |
Předmět: |
C57BL/6
medicine.medical_specialty biology business.industry medicine.medical_treatment Urology Toxicology medicine.disease biology.organism_classification Pathology and Forensic Medicine Surgery chemistry.chemical_compound chemistry In vivo Dysplasia Nitrosamine Toxicity medicine Carcinoma business Saline Carcinogen |
Zdroj: | Journal of Toxicologic Pathology. 16:19-23 |
ISSN: | 1881-915X 0914-9198 |
Popis: | The immunostimulatory α-galactosylceramide, KRN 7000 or (2S, 3S, 4R)-1-0-(α-D-galactopyranosyl)-2-(N-hexacosnoylamino)-1,3,4-octadecatrienol, might be anticipated to have antitumor activity in vivo apart from any direct toxicity to cancer cells. We investigated inhibition of mouse bladder carcinogenesis by intravesically instillated KRN 7000. C57BL/6 mice were divided into 4 groups; all first receiving the carcinogen 0.05% N-butyl-N-(4-hydroxybutyl)nitrosamine in drinking water for 8 weeks. Next, groups 1 and 2, respectively were administered 10 and 0.1 μg/kg of KRN 7000 intravesically once weekly for 17 weeks. Group 3 received only 0.3 ml of saline (vehicle control). Group 4 did not undergo bladder catheterization. By histologic examination at 26 weeks, the incidence of bladder carcinoma of all types tended to be higher in group 1 than in group 3, but without significance. The incidence of bladder carcinoma in group 4, (no catheterization), was similar to that in group 1. Only one precancerous lesion (papillary or nodular dysplasia) was seen in each of groups 3 and 4. Thus vesical instillation of KRN 7000 did not inhibit bladder carcinogenesis in mice, exposed to the carcinogen studied. |
Databáze: | OpenAIRE |
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