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Published on: August 6, 2014
The U.S. National Toxicology Program evaluation of transgenic mice as predictive models for identifying carcinogens
1Experimental Toxicology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA. eastin@niehs.nih.gov
Abstract:
National Institute of Environmental Health Sciences researchers have invested considerable effort in exploring the utility of transgenic mice to detect carcinogens and study mechanisms of carcinogenesis. Work has assessed several mouse models genetically altered to enhance their expression of chemically induced tumors. Results with the p53def (hemizygous for the tumor-suppressor gene) and the Tg.AC (carrier of an activated H-ras oncogene) mice have been used as a basis for a proposed new strategy for identifying chemical carcinogens and assessing risk. The U.S. National Toxicology Program is conducting a series of studies with these two transgenic strains to further examine their strengths and weaknesses for identification of documented rodent and human carcinogens and to explore their ability to provide information concerning the effective dosimetry for target organ mutation.
Insights
Researchers are evaluating genetically modified mouse models to detect carcinogens and understand cancer development. These transgenic mice, p53def and Tg.AC, show promise for identifying chemical carcinogens and assessing risk.
Area of Science:
- Environmental Health Sciences
- Toxicology
- Carcinogenesis Research
Background:
- Transgenic mouse models are valuable tools for studying chemical carcinogenesis.
- Genetically altered mice can enhance the expression of chemically induced tumors.
- Existing research has explored various mouse models for carcinogen detection.
Purpose of the Study:
- To evaluate the utility of p53def and Tg.AC transgenic mouse models for carcinogen detection.
- To investigate the mechanisms of carcinogenesis using genetically modified mice.
- To propose a new strategy for identifying chemical carcinogens and assessing risk.
Main Methods:
- Assessing genetically altered mouse models that enhance chemically induced tumors.
- Utilizing p53def (hemizygous for the tumor-suppressor gene) mice.
- Utilizing Tg.AC (carrier of an activated H-ras oncogene) mice.
Main Results:
- Results from p53def and Tg.AC mice form the basis of a proposed new strategy.
- These models are being studied to identify documented rodent and human carcinogens.
- The study explores the models' ability to provide information on effective dosimetry for target organ mutation.
Conclusions:
- Transgenic mouse models, specifically p53def and Tg.AC, offer a promising approach for carcinogen identification.
- These models can aid in understanding carcinogenesis mechanisms and risk assessment.
- Further studies are examining their strengths and weaknesses for regulatory toxicology.
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