拓扑异构酶
喜树碱
选择性
抗药性
劈理(地质)
细胞周期
化学
细胞凋亡
DNA
生物
癌症研究
药理学
生物化学
遗传学
断裂(地质)
古生物学
催化作用
作者
Yves Pommier,Philippe Pourquier,Yoshimasa Urasaki,Jiaxi Wu,Gary S. Laco
标识
DOI:10.1054/drup.1999.0102
摘要
Topoisomerase I (top1) inhibitors (camptothecins and other structurally diverse compounds) are effective and promising anticancer agents. Determinants of selectivity toward cancer cells and resistance are multifactorial. These factors can be separated in three groups. The first is related to alterations in drug distribution and metabolism. The second group includes both quantitative and qualitative (mutations) differences in top I. The third group includes resistance and sensitivity factors downstream from the cleavage complexes. They include DNA repair, cell cycle checkpoints and apoptosis, and are probably key to the relative selectivity of camptothecins toward cancer cells and to clinical resistance. Copyright 1999 Harcourt Publishers Ltd.
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