Ueda H, Manda T, Matsumoto S, Mukumoto S, Nishigaki F, Kawamura I, Shimomura K
Exploratory Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Ibaraki, Japan.
J Antibiot (Tokyo). 1994 Mar;47(3):315-23. doi: 10.7164/antibiotics.47.315.
The antitumor activities of FR901228, (E)-(1S,4S,10S,21R)-7-[(Z)- ethylidene]-4,21-diisopropyl-2-oxa-12,13-dithia-5,8,20,23- tetraazabicyclo[8,7,6]-tricos-16-ene-3,6,9,19,22-pentanone, isolated from Chromobacterium violaceum No. 968, were studied in animals. FR901228 (ip) prolonged the life of mice bearing such murine ascitic tumors as P388 and L1210 leukemias and B16 melanoma, and inhibited (iv) the growth of murine solid tumors (Colon 38 carcinoma, M5076 reticulum cell sarcoma and Meth A fibrosarcoma) and human solid tumors (Lu-65 and LC-6 lung carcinomas, and SC-6 stomach adenocarcinoma) implanted in normal and nude mice, respectively. Its antitumor activity was especially potent against murine Meth A fibrosarcoma and human SC-6 stomach adenocarcinoma which were refractory to mitomycin C or cisplatin. FR901228 also was more effective against mitomycin C-, cyclophosphamide-, vincristine- and 5-fluorouracil-resistant P388 leukemias than against non-resistant P388 in mice. These results suggest that FR901228 will be a new type of drug for the treatment of cancer.
对从紫色色杆菌968号菌株中分离得到的FR901228,即(E)-(1S,4S,10S,21R)-7-[(Z)-亚乙基]-4,21-二异丙基-2-氧杂-12,13-二硫杂-5,8,20,23-四氮杂双环[8,7,6]-二十三碳-16-烯-3,6,9,19,22-戊酮,进行了动物体内抗肿瘤活性研究。FR901228腹腔注射可延长携带P388和L1210白血病以及B16黑色素瘤等小鼠腹水瘤的小鼠生存期,静脉注射可抑制分别接种于正常小鼠和裸鼠体内的小鼠实体瘤(结肠38癌、M5076网状细胞肉瘤和Meth A纤维肉瘤)以及人实体瘤(Lu-65和LC-6肺癌以及SC-6胃腺癌)的生长。其抗肿瘤活性对丝裂霉素C或顺铂耐药的小鼠Meth A纤维肉瘤和人SC-6胃腺癌尤为显著。在小鼠中,FR901228对丝裂霉素C、环磷酰胺、长春新碱和5-氟尿嘧啶耐药的P388白血病的疗效比对非耐药P388白血病的疗效更佳。这些结果表明,FR901228将成为一种新型抗癌药物。