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dc.contributor.author | Snarskaya E. | |
dc.contributor.author | Pylev L. | |
dc.contributor.author | Akhunzyanov A. | |
dc.contributor.author | Kuznetсova E. | |
dc.date.accessioned | 2018-09-19T23:00:11Z | |
dc.date.available | 2018-09-19T23:00:11Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 2191-1630 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/145902 | |
dc.description.abstract | © 2016, Springer Science+Business Media New York.Previous studies have established that 7,12-dimethylbenz(a)anthracene (DMBA) can initiate skin tumorigenesis in conventional furred mouse models by acting on hair follicle stem cells. In this work, we have developed a simple and convenient rat model of basosquamous carcinoma (BSC) using DMBA-induced carcinogenesis in male specific pathogen free (SPF) Wistar rats with no additional tumor promoter agents. The results showed that topical application of 0.1% solution of DMBA in benzene in a volume of 40 μL twice a week produced skin tumors after 8–9 months. As a result, during the 11–12th months, we obtained 15 animals with BSCs, 22 with basal cell carcinomas (BCCs), and 3 with squamous cell carcinomas (SCCs). This chemically driven skin cancer model in Wistar rats can serve as a suitable alternative to the mouse skin cancer model and can be reliably replicated as demonstrated by the experiment. | |
dc.relation.ispartofseries | BioNanoScience | |
dc.subject | Basosquamous carcinoma | |
dc.subject | Chemical carcinogenesis | |
dc.subject | DMBA | |
dc.subject | Rat model | |
dc.title | Experimental Basosquamous Carcinoma Model in Rats | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 2 | |
dc.relation.ispartofseries-volume | 7 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 423 | |
dc.source.id | SCOPUS21911630-2017-7-2-SID85019143808 |