Jang J J, Takahashi M, Hasegawa R, Furukawa F, Toyoda K, Sato H, Miyakawa Y, Hayashi Y
Carcinogenesis. 1987 Aug;8(8):1149-53. doi: 10.1093/carcin/8.8.1149.
The oncogenic potential of adriamycin was studied in both sexes of Sprague-Dawley rats. Single i.v. injection of 10 or 2 mg and repeated injections of 2 mg of adriamycin/kg body wt within 2 weeks were performed on rats, 50 days old at the commencement. All surviving animals were killed at 52 weeks of the experiment. Multiple mammary tumors, mostly fibroadenomas, were observed in 30 and 41% of the females given single low (2 mg/kg) or repeated doses (5 X 2 mg/kg) respectively. These incidences were significantly higher than those for the corresponding control group (8%). Two male rats in the low dose group also developed mammary tumors. Both sexes receiving the single high dose (10 mg/kg) injection demonstrated early mortality due to marked toxicity. The mortality of five repeated-treatment group was lower than a single high-dose group. Renal cell tumors were evident in five rats of the single, low dose groups and dysplastic foci of renal tubular epithelium occurred in the groups given a single low or repeated doses of adriamycin. Thus the present experiment provides preliminary indication of carcinogenic potential of this chemotherapeutic agent for both kidney and mammary gland of Sprague-Dawley rats and further investigations are necessary to evaluate the carcinogenic risk of adriamycin treatment.
在雄性和雌性Sprague-Dawley大鼠中研究了阿霉素的致癌潜力。对实验开始时50日龄的大鼠静脉注射一次10或2 mg阿霉素,以及在2周内重复注射2 mg/kg体重的阿霉素。在实验的52周时处死所有存活的动物。分别在30%和41%单次给予低剂量(2 mg/kg)或重复给予(5×2 mg/kg)阿霉素的雌性大鼠中观察到多个乳腺肿瘤,大多为纤维腺瘤。这些发生率显著高于相应对照组(8%)。低剂量组中有两只雄性大鼠也发生了乳腺肿瘤。接受单次高剂量(10 mg/kg)注射的雌雄大鼠均因明显的毒性而早期死亡。五次重复治疗组的死亡率低于单次高剂量组。在单次低剂量组的五只大鼠中可见肾细胞肿瘤,在单次给予低剂量或重复给予阿霉素的组中出现肾小管上皮发育异常灶。因此,本实验初步表明这种化疗药物对Sprague-Dawley大鼠的肾脏和乳腺具有致癌潜力,有必要进行进一步研究以评估阿霉素治疗的致癌风险。