DNA topoisomerase II as the cellular target of a novel antitumor agent ICRF-193, a bisdioxopiperazine derivative, in Xenopus egg extract

被引:8
|
作者
Sato, M
Ishida, R
Ohsumi, K
Narita, T
Andoh, T
机构
[1] SOKA UNIV,FAC ENGN,DEPT BIOENGN,HACHIOJI,TOKYO 192,JAPAN
[2] ZENYAKU KOGYO CO LTD,RES LAB,NERIMA KU,TOKYO 178,JAPAN
[3] AICHI CANC CTR,RES INST,LAB CHEMOTHERAPY & BIOCHEM,CHIKUSA KU,NAGOYA,AICHI 464,JAPAN
[4] TOKYO INST TECHNOL,FAC BIOSCI,LAB CELL & DEV BIOL,MIDORI KU,YOKOHAMA,KANAGAWA 227,JAPAN
关键词
D O I
10.1006/bbrc.1997.6851
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have investigated the molecular target of an antitumor agent ICRF-193, a bisdioxopiperazine derivative, in in vitro chromosome condensation system of Xenopus egg extract (XEE), where DNA topoisomerase II was previously demonstrated to play a crucial role. Demembranated Xenopus sperm head chromatin is converted to metaphase chromosome-like structure in XEE in two steps, i.e., swelling of the chromatin followed by condensation of chromosome. When ICRF-193 was added to the reaction, swelling of the chromatin was not affected but chromosome condensation was completely blocked, This blockade was reversed by exogenous supplement of calf thymus topoisomerase II, which was in turn neutralized by anti-topoisomerase II monoclonal antibody. These results demonstrate that topoisomerase II is the molecular target of the drug ICRF-193. (C) 1997 Academic Press.
引用
收藏
页码:571 / 575
页数:5
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