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拓扑异构酶抑制剂作为有前景的抗癌药物的前景。

Prospects of Topoisomerase Inhibitors as Promising Anti-Cancer Agents.

作者信息

Yakkala Prasanna Anjaneyulu, Penumallu Naveen Reddy, Shafi Syed, Kamal Ahmed

机构信息

Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi 110062, India.

Department of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi 110062, India.

出版信息

Pharmaceuticals (Basel). 2023 Oct 13;16(10):1456. doi: 10.3390/ph16101456.

Abstract

Topoisomerases are very important enzymes that regulate DNA topology and are vital for biological actions like DNA replication, transcription, and repair. The emergence and spread of cancer has been intimately associated with topoisomerase dysregulation. Topoisomerase inhibitors have consequently become potential anti-cancer medications because of their ability to obstruct the normal function of these enzymes, which leads to DNA damage and subsequently causes cell death. This review emphasizes the importance of topoisomerase inhibitors as marketed, clinical and preclinical anti-cancer medications. In the present review, various types of topoisomerase inhibitors and their mechanisms of action have been discussed. Topoisomerase I inhibitors, which include irinotecan and topotecan, are agents that interact with the DNA-topoisomerase I complex and avert resealing of the DNA. The accretion of DNA breaks leads to the inhibition of DNA replication and cell death. On the other hand, topoisomerase II inhibitors like etoposide and teniposide, function by cleaving the DNA-topoisomerase II complex thereby effectively impeding the release of double-strand DNA breaks. Moreover, the recent advances in exploring the therapeutic efficacy, toxicity, and MDR (multidrug resistance) issues of new topoisomerase inhibitors have been reviewed in the present review.

摘要

拓扑异构酶是调节DNA拓扑结构的非常重要的酶,对DNA复制、转录和修复等生物学行为至关重要。癌症的发生和扩散与拓扑异构酶失调密切相关。拓扑异构酶抑制剂因其能够阻碍这些酶的正常功能,导致DNA损伤并随后引起细胞死亡,因而成为潜在的抗癌药物。本综述强调了拓扑异构酶抑制剂作为已上市、临床和临床前抗癌药物的重要性。在本综述中,讨论了各种类型的拓扑异构酶抑制剂及其作用机制。拓扑异构酶I抑制剂,包括伊立替康和拓扑替康,是与DNA-拓扑异构酶I复合物相互作用并避免DNA重新封闭的药物。DNA断裂的增加导致DNA复制的抑制和细胞死亡。另一方面,拓扑异构酶II抑制剂如依托泊苷和替尼泊苷,通过切割DNA-拓扑异构酶II复合物起作用,从而有效地阻止双链DNA断裂的释放。此外,本综述还回顾了探索新型拓扑异构酶抑制剂的治疗效果、毒性和多药耐药性(MDR)问题的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/264b/10609717/db02ee15cc25/pharmaceuticals-16-01456-g001.jpg

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