Alison R H, Capen C C, Prentice D E
Department of Veterinary Pathobiology, Ohio State University, Columbus 43210.
Toxicol Pathol. 1994 Mar-Apr;22(2):179-86. doi: 10.1177/019262339402200211.
Many compounds giving a positive result in animal carcinogenicity studies through mechanisms involving secondary carcinogenesis pose little or no risk to humans. This article provides an overview of current understanding, with particular reference to renal tumors in male rats with alpha 2mu-globulin nephropathy, urinary bladder neoplasia in rodents, mesovarian leiomyomas induced in rats by beta 2-receptor stimulants, carcinoid tumors in the rodent stomach induced by prolonged suppression of acid secretion, thyroid follicular cell tumors in rodents, canine mammary neoplasia due to administration of progestagens, rodent mammary neoplasia induced by estrogens, uterine endometrial carcinomas of rats induced by dopamine agonists, Leydig cell tumors in the testis of rats, and ovarian tubulostromal adenomas in mice. A positive result on a rodent carcinogenicity study should not automatically preclude further development of a compound; future progress in this field should increase the accuracy of the rodent carcinogenicity study as a tool in human safety assessment.
许多通过涉及继发性致癌机制在动物致癌性研究中得出阳性结果的化合物对人类的风险很小或没有风险。本文概述了当前的认识,特别提及了患有α2μ球蛋白肾病的雄性大鼠的肾肿瘤、啮齿动物的膀胱肿瘤、β2受体兴奋剂在大鼠中诱发的卵巢系膜平滑肌瘤、长期抑制胃酸分泌在啮齿动物胃中诱发的类癌肿瘤、啮齿动物的甲状腺滤泡细胞肿瘤、因使用孕激素导致的犬乳腺肿瘤、雌激素诱发的啮齿动物乳腺肿瘤、多巴胺激动剂诱发的大鼠子宫内膜癌、大鼠睾丸的 Leydig 细胞瘤以及小鼠的卵巢小管间质腺瘤。啮齿动物致癌性研究的阳性结果不应自动排除化合物的进一步研发;该领域未来的进展应提高啮齿动物致癌性研究作为人类安全评估工具的准确性。