• 1 January 1979
    • journal article
    • research article
    • Vol. 39 (9), 3419-3428
Abstract
Clofibrate (ethyl chlorophenoxyisobutyrate, Atromid-S), because it contains a chlorinated phenoxy moiety and is the most commonly used hypolipidemic drug in the USA and Europe, was fed at a concentration of 0.5% in the diet of 25 male F344 rats for 72-97 wk, and the animals were inspected for tumors up to a maximum of 129 wk. Between 72 and 129 wk, there were 10 rats with a total of 16 tumors. These included 4 hepatocellular carcinomas, an adenocarcinoma of the glandular stomach, papillary carcinoma of the urinary bladder, acinar cell carcinoma of the pancreas, lymphosarcoma involving pancreas, acinar cell adenomas of the pancreas, renal carcinoma and sarcomas of the lung and parotid gland. Although the number of experimental animals was small, none of these tumors were present in 25 controls, and systematic examination of available literature dealing with spontaneous tumors in several thousand rats indicated that the tumors in clofibrate-fed rats were not spontaneous. A number of the tumors were transplanted through several generations. Clofibrate, like 2 other hypolipidemic drugs that are carcinogenic, causes peroxisome proliferation. Some drugs that cause peroxisome proliferation may represent a new class of chemical carcinogens. There may be a relationship between peroxisome proliferation and malignant transformation.