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 |
|