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Spontaneous and chemically induced proliferative lesions in Tg.AC transgenic and p53-heterozygous mice

J F Mahler1, N D Flagler, D E Malarkey

  • 1National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.

Toxicologic Pathology
|August 26, 1998
PubMed

Insights

Genetically altered mouse models, including Tg.AC transgenic and p53-deficient mice, are valuable tools for carcinogen detection. These studies provide extensive toxicologic pathology data, aiding in the assessment of chemical exposures.

Area of Science:

  • Toxicologic Pathology
  • Genetically Altered Mouse Models
  • Carcinogen Detection

Background:

  • Genetically altered mouse models are increasingly used for carcinogen detection.
  • The National Toxicology Program (NTP) has conducted extensive studies using these models.
  • Large datasets of toxicologic pathology are emerging for these strains.

Purpose of the Study:

  • To evaluate genetically altered mouse models for short-term carcinogen detection.
  • To describe proliferative target organ effects in Tg.AC and p53-deficient mice.
  • To present the tumor profile in control groups of these mouse models.

Main Methods:

  • Utilized Tg.AC transgenic mice.
  • Employed heterozygous p53-deficient mice.
  • Analyzed data from short-term chemical exposure studies.

Main Results:

  • Observed proliferative target organ effects in the evaluated mouse models.
  • Characterized tumor profiles in control groups.
  • Accumulated significant toxicologic pathology data.

Conclusions:

  • Tg.AC transgenic and p53-deficient mice are important models in toxicologic pathology.
  • These models contribute significantly to carcinogen detection efforts.
  • The findings offer a comprehensive toxicologic assessment of these mouse strains.

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