THE LINKING OF ANTICANCER DRUGS, CELL-CYCLE BLOCKS, AND DIFFERENTIATION - IMPLICATIONS IN THE SEARCH FOR ANTINEOPLASTIC DRUGS

被引:5
作者
DINNEN, RD [1 ]
EBISUZAKI, K [1 ]
机构
[1] UNIV WESTERN ONTARIO,HLTH SCI CTR,DEPT BIOCHEM,LONDON N6A 5C1,ONTARIO,CANADA
关键词
ANTICANCER DRUGS; CELL CYCLE; DIFFERENTIATION; COMMITMENT; ERYTHROLEUKEMIA; MURINE;
D O I
10.1016/0145-2126(92)90175-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The quest for anticancer drugs has been primarily directed at agents that interfere with cell replication, vet the basis for drug-induced cytotoxicity remains unsolved. In our previous studies we noted a relationship between a mitotic block and commitment to terminal differentiation in the murine (Friend) erythroleukemia (FEL) cell. Since anticancer drugs are known to often block cell cycle transit typically in G2/mitosis, we tested a number of anticancer drugs with various modes of action and found that they all committed FEL cells to differentiate. Furthermore. other G2/mitosis-blocking drugs were also effective in inducing commitment. These results suggest (1) a causal relationship involving anticancer drugs, cell cycle block and differentiation, (2) that the search for new anticancer drugs utilize a differentiation assay and include G2/mitosis-blocking agents.
引用
收藏
页码:491 / 495
页数:5
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