Rustia M, Shubik P
Br J Cancer. 1978 Aug;38(2):237-49. doi: 10.1038/bjc.1978.194.
Griseofulvin, an antibiotic used to treat dermatophystosis, was tested for carcinogenicity in mice, rats and hamsters. Three groups of mice and rats were given the drug in powdered diet in alternating 5-week periods for life, at dose levels of 3.0%, 1.5% and 0.3% (mice) and 2.0%, 1.0% and 0.2% (rats). A group of mice and 3 groups of hamsters received continuous daily treatment for life with griseofulvin at 3.0%, 1.5%, 0.3% and 0.1% dose levels respectively. A significant incidence of hepatic tumours was observed at the 2 higher treatment levels in mice. Also, statistically significant rates (P less than or equal to 0.001 and/or P less than or equal to 0.020) of thyroid tumours, indicating a dose-response, were recorded in male rats at the 2.0%, 1.0%, and 0.2% dose levels, and in females at the 2.0% and 1.0% dose levels. Hamsters did not develop neoplasms in response to treatment at any level.
用于治疗皮肤癣菌病的抗生素灰黄霉素,在小鼠、大鼠和仓鼠身上进行了致癌性测试。三组小鼠和大鼠在其一生中,以5周为一个交替周期,食用添加了该药物的粉末状饲料,剂量水平分别为3.0%、1.5%和0.3%(小鼠)以及2.0%、1.0%和0.2%(大鼠)。一组小鼠和三组仓鼠在其一生中分别以3.0%、1.5%、0.3%和0.1%的剂量水平接受灰黄霉素的每日持续治疗。在小鼠中,较高的两个治疗水平观察到肝脏肿瘤的显著发生率。此外,在2.0%、1.0%和0.2%剂量水平的雄性大鼠以及2.0%和1.0%剂量水平的雌性大鼠中,记录到甲状腺肿瘤的发生率具有统计学意义(P小于或等于0.001和/或P小于或等于0.020),表明存在剂量反应。仓鼠在任何治疗水平下均未出现肿瘤。