trans-4-Acetylaminostilbene is acutely toxic to the glandular stomach and produces sebaceous gland
tumors in rats quite specifically. Metabolism, tissue exposure to reactive metabolites,
DNA binding and persistence of DNA lesions are implicated in tissue susceptibility, but nothing indicates that one of these parameters determines the
biological effect. All tissues are exposed to reactive metabolites, liver as a nontarget tissue ranking highest.
DNA binding in this tissue, however, is not irrelevant to
tumor formation, but rather indicates the presence of initiating lesions. They can be amplified by partial
hepatectomy and/or promoters, such as
phenobarbital,
DDT and
diethylstilbestrol. Liver
tumors are formed in high yields with these treatments, and mammary
tumors also occur.
trans-4-Acetylaminostilbene is therefore considered to be an incomplete
carcinogen in these tissues and may initiate cells in other tissues as well. Apparently it lacks promoting properties which are supposed to be unrelated to reactive metabolites. It is concluded that DNA lesions do not reflect tissue risk, but rather secondary effects ultimately determine where the process of
tumor formation starts and how fast it develops.