The liver is a major target organ in rodent carcinogenicity assays. Am
ongst the agents that are effective in producing rodent liver tumours
are many chemicals which are not mutagenic, but are believed to mediat
e their effects by promoting the clonal outgrowth of initiated cells.
Some of these chemicals, such as dibenzo-p-dioxins and certain PCBs, h
ave been demonstrated to interact with specific cellular receptors and
receptor binding appears crucial for their tumourigenic activity. Enz
yme-altered foci in rat liver may serve as a sensitive means to estima
te the promoting activity of these agents in rodents. Mechanistic cons
iderations are of relevance when extrapolating these data from rodents
to humans.