Carr B I, Reilly J G, Smith S S, Winberg C, Riggs A
Carcinogenesis. 1984 Dec;5(12):1583-90. doi: 10.1093/carcin/5.12.1583.
5-Azacytidine was administered to young adult male Fischer rats. Tumors were found in 31 out of 70 rats that had received 5-azacytidine and survived 18 months from the start of the experiment. Several rats had multiple primary tumors. In the rats that were tested for complete carcinogenicity a variety of tumor types was found. These included acute leukemia and malignant reticuloendotheliosis, and tumors of the testis, skin, and bronchus. No hepatic tumors were found in the group that was tested for hepatic tumor initiation. Hepatocellular carcinomas were found only in the group that was examined for hepatic tumor promotion by receiving a prior initiating dose of diethylnitrosamine. No tumors were found in the age controls. Thus, in these initial experiments, 5-azacytidine appeared to be a complete carcinogen, inducing tumors in several organs, and a tumor promoter but not a complete carcinogen for the liver.
对年轻成年雄性Fischer大鼠施用5-氮杂胞苷。在70只接受5-氮杂胞苷且从实验开始存活18个月的大鼠中,有31只发现了肿瘤。几只大鼠有多个原发性肿瘤。在进行完全致癌性测试的大鼠中,发现了多种肿瘤类型。这些包括急性白血病和恶性网状内皮组织增生症,以及睾丸、皮肤和支气管肿瘤。在进行肝肿瘤起始测试的组中未发现肝肿瘤。仅在接受先前起始剂量二乙基亚硝胺进行肝肿瘤促进检查的组中发现肝细胞癌。在年龄对照组中未发现肿瘤。因此,在这些初步实验中,5-氮杂胞苷似乎是一种完全致癌物,可在多个器官中诱导肿瘤,并且是一种肿瘤促进剂,但不是肝脏的完全致癌物。