Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 2012-01-01

The rainbow trout liver cancer model: Response to environmental chemicals and studies on promotion and chemoprevention

David E. Williams, David E Williams, David E Williams

Index: Comp. Biochem. Physiol. C. Toxicol. Pharmacol. 155(1) , 121-7, (2012)

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Abstract

Rainbow trout ( Oncorhynchus mykiss) are an outstanding model of liver cancer induction by environmental chemicals and development of strategies for chemoprevention. Trout have critical and unique advantages allowing for cancer studies with 40,000 animals to determine dose–response at levels orders of magnitude lower than possible in rodents. Examples of two promoters in this model, the dietary supplement dehydroepiandrosterone (DHEA) and industrial chemical perfluorooctanoic acid (PFOA), are presented. In addition, indole-3-carbinol (I3C) and chlorophyllin (CHL) inhibit initiation following exposure to potent human chemical carcinogens (e.g., aflatoxin B 1 (AFB 1)). Two “ED 001” cancer studies have been conducted, utilizing approximately 40,000 trout, by dietary exposure to AFB 1 and dibenzo[ d,e,f,p]chrysene (DBC). These studies represent the two largest cancer studies ever performed and expand the dose–response dataset generated by the 25,000 mouse “ED 01” study over an order of magnitude. With DBC, the liver tumor response fell well below the LED 10 line, often used for risk assessment, even though the biomarker (liver DBC–DNA adducts) remained linear. Conversely, the response with AFB 1 remained relatively linear throughout the entire dose range. These contributions to elucidation of mechanisms of liver cancer, induced by environmental chemicals and the remarkable datasets generated with ED 001 studies, make important contributions to carcinogenesis and chemoprevention.