Selection of cancer chemopreventive agents based on inhibition of topoisomerase II activity

被引:39
作者
Cho, KH
Pezzuto, JM
Bolton, JL
Steele, VE
Kelloff, GJ
Lee, SK
Constantinou, A
机构
[1] Univ Illinois, Coll Med, Dept Surg Oncol, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Pharm, Dept Med Chem & Pharmacognosy, Chicago, IL 60612 USA
[3] NCI, Chemoprevent Branch, Div Canc Prevent, NIH, Bethesda, MD 20892 USA
[4] Ewha Womans Univ, Coll Pharm, Seodaemun Ku, Seoul 120750, South Korea
关键词
topoisomerase I; topoisomerase II; chemoprevention; unknotting assay; relaxation assay; organoselenium; carcinogenesis; selectivity; specificity; predictive value;
D O I
10.1016/S0959-8049(00)00300-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present study was undertaken to determine if in vitro inhibition of one or both of the two most dominant mammalian DNA topoisomerases (topos) is common among chemopreventive agents. To determine if an agent was a topo I inhibitor, we employed the DNA relaxation and nicking assays. For potential topo II inhibitors, we used the DNA unknotting and linearisation assays. 14 of 30 agents (47%) were ineffective in all four assays (IC50 > 100 mug/ml), and 11 (37%) inhibited topo II catalytic activity. The sensitivity of the topo II assay was 63%, selectivity 93%, positive predictive value 91%. and total accuracy 77%. For chemopreventive efficacy, the positive predictive value of the unknotting assay was 92%, and the total accuracy was 60%. These data suggest that reduced topo II activity is a desirable property of many known chemopreventive agents. We conclude that the unknotting assay could be a valuable addition to the in vitro tests presently used to select chemopreventive agents. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2146 / 2156
页数:11
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