A 90-day drinking water study in mice to characterize early events in the cancer mode of action of 1,4-dioxane
Autor: | Joanna Klapacz, Richard C. Pleus, Matthew J. LeBaron, Lisa M. Corey, Robert A. Budinsky, James Crissman, Rachel M. Golden, Mark Lafranconi |
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Rok vydání: | 2020 |
Předmět: |
Rodent
Carcinogenesis Cell Survival Physiology 010501 environmental sciences Toxicology 030226 pharmacology & pharmacy 01 natural sciences Muscle hypertrophy Dioxanes 03 medical and health sciences Mice 0302 clinical medicine biology.animal Medicine Animals Mode of action 0105 earth and related environmental sciences Cell Proliferation biology Dose-Response Relationship Drug business.industry Drinking Water Liver Neoplasms Toxicity Tests Subchronic Cancer General Medicine medicine.disease Vacuolization Liver Apoptosis Carcinogens Tumor promotion Female business |
Zdroj: | Regulatory toxicology and pharmacology : RTP. 119 |
ISSN: | 1096-0295 |
Popis: | Studies demonstrate that with sufficient dose and duration, 1,4-dioxane (1,4-DX) induces liver tumors in laboratory rodent models. The available evidence aligns with a threshold-dependent, tumor promotion mode of action (MOA). The MOA and key events (KE) in rats are well developed but less so in the mouse. Therefore, we conducted a 90-day drinking water study in female mice to evaluate early KE at 7, 28, and 90 days. Female B6D2F1/Crl mice consumed drinking water containing 0, 40, 200, 600, 2000 or 6000 ppm 1,4-DX. 1,4-DX was detected in blood at 90-days of exposure to 6000 ppm, but not in the other exposure groups, indicating a metabolic clearance threshold between 2000 and 6000. Early events identified in this study include glycogen-like vacuolization, centrilobular hypertrophy, centrilobular GST-P staining, apoptosis, and pan-lobular increase in cell proliferation observed after 90-days of exposure to 6000 ppm 1,4-DX. There was minimal evidence of hepatotoxicity over the duration of this study. These findings demonstrate a previously unreported direct mitogenic response following exposures exceeding the metabolic clearance threshold of 1,4-DX. Collectively, the information generated in this study supports a threshold MOA for the development of liver tumors in mice after exposure to 1,4-DX. |
Databáze: | OpenAIRE |
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