ED-110, A NOVEL INDOLOCARBAZOLE, PREVENTS THE GROWTH OF EXPERIMENTAL-TUMORS IN MICE

被引:24
作者
ARAKAWA, H [1 ]
IGUCHI, T [1 ]
YOSHINARI, T [1 ]
KOJIRI, K [1 ]
SUDA, H [1 ]
OKURA, A [1 ]
机构
[1] MERCK RES LABS,BANYU TSUKUBA RES INST,OKUBO 3,TSUKUBA 30033,JAPAN
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1993年 / 84卷 / 05期
关键词
TOPOISOMERASE-I; ANTITUMOR AGENT; ED-110; INDOLOCARBAZOLE;
D O I
10.1111/j.1349-7006.1993.tb00178.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A new indolocarbazole compound, ED-110, which was obtained by glucosylating a microbial product (BE-13793C) and is a potent topoisomerase I inhibitor, showed characteristic inhibitory effects on the growth of 12 human tumor cell lines tested. The IC50 values of ED-110 against 9 of the 12 lines ranged from 11.5 mug/ml to 0.07 mug/ml, while the remaining 3 lines were quite resistant (IC50, > 100 mug/ml). In in vivo experiments, i.p. treatment with ED-110 increased the survival period by more than two-fold in mice implanted i.p. with P388, L1210, L5178Y or EL4 murine leukemic cells. The minimum effective dose increasing the life-span of mice bearing P388 leukemia by 25 % was < 2.5 mg/kg/day x 10 and the maximum tolerated dose was >160 mg/kg/day x 10. ED-110 was also effective against the spontaneous metastasis of mouse Meth A fibrosarcoma cells and the growth of xenografted MKN-45 human stomach cancer cells as well as s.c. implanted mouse colon 26 and IMC carcinoma cells. These results indicated that ED-110 may have potential as a new antineoplastic agent with a large chemotherapeutic index and a wide range of effective doses.
引用
收藏
页码:574 / 581
页数:8
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