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Updated: Aug 18, 2026

High Content Screening Analysis to Evaluate the Toxicological Effects of Harmful and Potentially Harmful Constituents (HPHC)
Published on: May 10, 2016
Bioassay of 2, 4, 5-trichlorophenoxyacetic acid for carcinogenicity in mice
Abstract:
Adult mice of strains C3Hf and XVII/G received 2, 4, 5-T by continuous oral administration (80 ppm in the diet). The 2, 4, 5-T preparation contained less than 0-05 ppm of dioxins. In 2, 4, 5-T -treated C3Hf mice a significant increase in the incidence of neoplastic lesions was found. No significant difference was found in the XVII/G strain between the treated and control mice. Rare forms of tumours, which were not observed in the controls, were present in the 2, 4, 5-t -treated C3Hf mice.
Insights
This study found that 2,4,5-T exposure increased neoplastic lesions in C3Hf mice but not XVII/G mice. Rare tumors appeared in treated C3Hf mice, suggesting strain-specific carcinogenicity.
Area of Science:
- Toxicology
- Carcinogenesis
- Animal Models
Background:
- 2,4,5-Trichlorophenoxyacetic acid (2,4,5-T) is a herbicide with potential health risks.
- Dioxin contamination in 2,4,5-T preparations is a known concern.
- Understanding the carcinogenic potential of 2,4,5-T in different genetic backgrounds is crucial.
Purpose of the Study:
- To investigate the carcinogenic effects of 2,4,5-T in adult mice.
- To compare the susceptibility of different mouse strains (C3Hf and XVII/G) to 2,4,5-T-induced neoplasia.
- To identify any novel or rare tumor types associated with 2,4,5-T exposure.
Main Methods:
- Adult mice of C3Hf and XVII/G strains were administered 2,4,5-T orally (80 ppm in diet).
- The 2,4,5-T preparation was analyzed for dioxin content (<0.05 ppm).
- Incidence of neoplastic lesions and tumor types were compared between treated and control groups for each strain.
Main Results:
- A significant increase in neoplastic lesions was observed in 2,4,5-T-treated C3Hf mice compared to controls.
- No significant difference in neoplastic lesions was found between treated and control XVII/G mice.
- Rare tumor forms, not seen in controls, were present in the 2,4,5-T-treated C3Hf mice.
Conclusions:
- The C3Hf mouse strain exhibits increased susceptibility to 2,4,5-T-induced carcinogenesis.
- The XVII/G mouse strain appears resistant to the carcinogenic effects of 2,4,5-T under these experimental conditions.
- 2,4,5-T exposure can lead to the development of rare and potentially novel neoplastic lesions in susceptible mouse strains.
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