Beck W T, Danks M K
Department of Biochemical and Clinical Pharmacology, St Jude Children's Research Hospital, Memphis, TN 38101.
Semin Cancer Biol. 1991 Aug;2(4):235-44.
DNA topoisomerases are essential nuclear enzymes that are involved in DNA replication. Clinically useful antitumor drugs such as doxorubicin, daunorubicin (anthracyclines), etoposide, teniposide (epipodophyllotoxins), and amsacrine (an aminoacridine) interfere with the function of topoisomerase II and camptothecin and its analogs inhibit topoisomerase I. Some mammalian tumor cells that express resistance to drugs that interfere with topoisomerase I or topoisomerase II have alterations in their respective topoisomerases. In this paper, we review the functions of the topoisomerases, discuss aspects of their cellular regulation, ask how interference with topoisomerase function can lead to tumor cell death, discuss the biochemical features of tumor cells that are resistant to these anti-topoisomerase drugs, and, in the context of drug resistance, we raise questions about how these drugs exert their cytotoxicity.
DNA拓扑异构酶是参与DNA复制的重要核酶。临床上有用的抗肿瘤药物,如阿霉素、柔红霉素(蒽环类)、依托泊苷、替尼泊苷(表鬼臼毒素)和安吖啶(一种氨基吖啶)会干扰拓扑异构酶II的功能,而喜树碱及其类似物则抑制拓扑异构酶I。一些对干扰拓扑异构酶I或拓扑异构酶II的药物产生抗性的哺乳动物肿瘤细胞,其各自的拓扑异构酶发生了改变。在本文中,我们回顾了拓扑异构酶的功能,讨论了它们的细胞调控方面,探讨了干扰拓扑异构酶功能如何导致肿瘤细胞死亡,讨论了对这些抗拓扑异构酶药物耐药的肿瘤细胞的生化特征,并且在耐药性的背景下,我们提出了关于这些药物如何发挥细胞毒性的问题。