ANTITUMOR-ACTIVITY OF A NOVEL NUCLEOSIDE, 2'-C-CYANO-2'-DEOXY-1-BETA-D-ARABINOFURANOSYLCYTOSINE (CNDAC) AGAINST MURINE AND HUMAN TUMORS

被引:70
|
作者
TANAKA, M
MATSUDA, A
TERAO, T
SASAKI, T
机构
[1] KANAZAWA UNIV,CANC RES INST,DEPT EXPTL THERAPEUT,13-1 TAKARAMACHI,KANAZAWA,ISHIKAWA 920,JAPAN
[2] HOKKAIDO UNIV,FAC PHARMACEUT SCI,SAPPORO,HOKKAIDO 060,JAPAN
关键词
2'-C-CYANO-2'-DEOXY-1-BETA-D-ARABINOFURANOSYLCYTOSINE; ANTITUMOR ACTIVITY; HUMAN CANCER; MTT-ASSAY; CHICK EMBRYO ASSAY; NUDE MOUSE ASSAY;
D O I
10.1016/0304-3835(92)90024-P
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The antitumor effects of 2'-C-cyano-2'-deoxy-1-beta-D-arabinofuranosylcytosine (CNDAC), a synthetic 1-beta-D-arabinofuranosylcytosine (ara-C) derivative, were examined and compared with that of ara-C in murine tumors and in various human tumors using three different chemosensitivity tests. CNDAC extended the life span of mice bearing P388 leukemia. CNDAC had a unique in vitro antitumor spectrum for human cancers different from that of ara-C. Compared with ara-C, CNDAC was more effective in 10 human tumors (2 lung, 4 stomach and 4 osteosarcoma), equal in 2 tumors (lung and fibrosarcoma) and less potent in 11 tumors (4 lung, 4 osteosarcoma, bladder, renal and epidermoid). Characteristically CNDAC showed excellent activities against tumors, refractory to ara-C, such as HT-1080 human fibrosarcoma implanted in chick embryos or athymic mice, although its cytotoxicity against HT-1080 was almost equal to that of ara-C. Thus, CNDAC is an interesting and promising agent that should be considered for further detailed preclinical evaluation.
引用
收藏
页码:67 / 74
页数:8
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