neoplasm
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• mutants show a papilloma multiplicity similar to wild-type after DMBA/TPA treatment, however tumors that develop are larger than in wild-type
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• tumor development is similar to wild-type after DMBA/TPA treatment although tumors are flatter and grow in an endophytic pattern compared to a highly exophytic pattern
• however, tumor progression is accelerated compared to single Trp53 homozygotes
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• carcinoma latency and multiplicity after DMBA/TPA is similar to that seen in single homozygous Cdkn2a mutants, however size of carcinomas is larger than in wild-type or in single Trp53 mutants
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