neoplasm
• spontaneous squamous cell carcinomas (SCC) formation in 64 out of 176 transgenic mice
• develop multiple tumors between 5 and 8 weeks
• enlarged keratinocytes with nuclear atypia, mitotic activity, dermal invasion, and focal keratinization in SCC
• no metastasis after following for at least 6 months
|
integument
• hyperkeratosis in punctate hyperkeratotic lesions
|
• parakeratosis (retained nuclei in the stratum corneum) in punctate hyperkeratotic lesions
|
• cytologic atypia and architectural disorganization in hyperkeratotic plaques and lesions
• increased mitotic activity in hyperkeratotic plaques
• enlarged keratinocytes with nuclear atypia, mitotic activity, dermal invasion, and focal keratinization in SCC
|
• keratinocyte dysplasia in punctate hyperkeratotic lesions
|
• 135 out of 176 transgenic mice develop hyperkeratotic plaques within 4 days postnatal
• punctate (1-3 mm) hyperkeratotic lesions (resembling a human actinic keratosis) at 4 to 5 weeks
|
• markedly thickened epidermis in hyperkeratotic plaques
|
• spontaneous squamous cell carcinomas (SCC) formation in 64 out of 176 transgenic mice
• develop multiple tumors between 5 and 8 weeks
• enlarged keratinocytes with nuclear atypia, mitotic activity, dermal invasion, and focal keratinization in SCC
• no metastasis after following for at least 6 months
|
cellular
• keratinocyte dysplasia in punctate hyperkeratotic lesions
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
skin squamous cell carcinoma | DOID:3151 | J:155536 |