neoplasm
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• focal low grade PIN are seen at 10 - 14 months of age
• by 15 - 20 months of age both focal low grade and high grade PIN are seen
• the incidence of high grade PIN is increased in mutant mice homozygous for the Trp53 allele relative to mice heterozygous for the Trp53 allele
• levels of cell proliferation are 9 fold higher in PIN lesions
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reproductive system
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• focal hyperplasia is seen beginning at 10 -14 months of age
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|
• focal low grade PIN are seen at 10 - 14 months of age
• by 15 - 20 months of age both focal low grade and high grade PIN are seen
• the incidence of high grade PIN is increased in mutant mice homozygous for the Trp53 allele relative to mice heterozygous for the Trp53 allele
• levels of cell proliferation are 9 fold higher in PIN lesions
|
|
• areas of hyperplasia are positive for markers of DNA damage
• 4 fold increase in apoptotic cells in PIN foci
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endocrine/exocrine glands
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• focal hyperplasia is seen beginning at 10 -14 months of age
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|
• focal low grade PIN are seen at 10 - 14 months of age
• by 15 - 20 months of age both focal low grade and high grade PIN are seen
• the incidence of high grade PIN is increased in mutant mice homozygous for the Trp53 allele relative to mice heterozygous for the Trp53 allele
• levels of cell proliferation are 9 fold higher in PIN lesions
|
|
• areas of hyperplasia are positive for markers of DNA damage
• 4 fold increase in apoptotic cells in PIN foci
|