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Non-Camptothecin DNA Topoisomerase I Inhibitors in Cancer Therapy

机译:非喜树碱DNA拓扑异构酶I抑制剂在癌症治疗中。

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摘要

Human DNA topoisomerase I is the target of camptothecins, which have been recently introduced in the clinic for cancer chemotherapy. The discovery of novel noncamptothecin inhibitors is facilitated by the availability of biochemical and cellular assays for testing topoisomerase I activity. Among the non-camptothecin inhibitors, the indolocarbazoles (NB-506 and J-107088) are the most advanced in their development, and are in clinical trials. A number of indenoisoquinolines and minor groove binders (benzimidazoles) have been reported recently. Their antitumor activity is promising for further development. The potential binding site(s) of topoisomerase I inhibitors in the enzyme I-DNA complex is discussed.
机译:人DNA拓扑异构酶I是喜树碱的靶标,喜树碱最近已在癌症化疗的临床中引入。新型非喜树碱抑制剂的发现可通过用于测试拓扑异构酶I活性的生化和细胞分析来促进。在非喜树碱抑制剂中,吲哚并咔唑(NB-506和J-107088)在其研发中最为先进,并且正在临床试验中。最近已经报道了许多茚并异喹啉和小沟粘合剂(苯并咪唑)。它们的抗肿瘤活性有望进一步发展。讨论了酶I-DNA复合物中拓扑异构酶I抑制剂的潜在结合位点。

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