Moriuchi S, Shimizu K, Yamada M, Mabuchi E, Tamura K, Park K, Hayakawa T, Mogami H
Department of Neurological Surgery, Osaka University Medical School.
Nihon Gan Chiryo Gakkai Shi. 1990 Dec 20;25(12):2774-80.
FK973, a novel antitumor antibiotic, was obtained as a fermentation product of Streptomyces sandaensis. FK973 had excellent cytotoxic effects against in vitro cultured human glioblastomas, medulloblastomas, and murine glioma (203 glioma) cells. The antitumor effects were also well observed against ACNU resistant glioma cells. FK973 did not go through the blood-brain barrier. The median survival time (MST) of MG models treated with FK973 was 21 days. On the other hand, the MST of the control group was 15 days. In the in vitro assessment against neural disturbance, FK973 showed a little disturbance of murine brain cells but less toxic than ADM. In the in vivo neurotoxicity examination, FK973 showed no clear damage to the neural cells and myelin sheaths.
新型抗肿瘤抗生素FK973是三田链霉菌的发酵产物。FK973对体外培养的人胶质母细胞瘤、髓母细胞瘤和鼠胶质瘤(203胶质瘤)细胞具有优异的细胞毒性作用。对ACNU耐药的胶质瘤细胞也观察到了良好的抗肿瘤效果。FK973不能透过血脑屏障。用FK973治疗的MG模型的中位生存时间(MST)为21天。另一方面,对照组的MST为15天。在针对神经干扰的体外评估中,FK973对鼠脑细胞有轻微干扰,但毒性低于阿霉素。在体内神经毒性检查中,FK973对神经细胞和髓鞘没有明显损伤。