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DNA拓扑异构酶相关疗法的发展:新挑战的简要展望。

Development of DNA topoisomerase-related therapeutics: a short perspective of new challenges.

作者信息

Capranico Giovanni, Zagotto Giuseppe, Palumbo Manlio

机构信息

Department of Biochemistry G. Moruzzi, Alma Mater Studiorum University of Bologna, via Irnerio 48, 40126 Bologna, Italy.

出版信息

Curr Med Chem Anticancer Agents. 2004 Jul;4(4):335-45. doi: 10.2174/1568011043352885.

Abstract

Antitumor agents targeting DNA and DNA-associated processes are widely used in the treatment of human cancers and produce significant increases in the survival of patients. DNA topoisomerases remain the most significant target of these cytotoxic drugs and constitute a growing family of nuclear enzymes that regulate DNA topology during DNA replication and recombination, DNA transcription, chromosome condensation-decondensation and segregation. Major progress has been attained in recent years in the understanding of the structures of these enzymes and their main cellular functions, hopefully providing new opportunities for pharmacological interventions. New leads and derivatives of known structures have been reported recently, and here they will be discussed highlighting the challenges to find innovative and more effective drugs. Moreover, we will review novel and diverse approaches relevant to the development of new topoisomerase-related therapeutics.

摘要

靶向DNA及与DNA相关过程的抗肿瘤药物在人类癌症治疗中被广泛应用,显著提高了患者的生存率。DNA拓扑异构酶仍然是这些细胞毒性药物最重要的靶点,并且构成了一个不断壮大的核酶家族,该家族在DNA复制与重组、DNA转录、染色体凝聚-解聚及分离过程中调节DNA拓扑结构。近年来,在理解这些酶的结构及其主要细胞功能方面取得了重大进展,有望为药物干预提供新的机会。最近报道了已知结构的新先导物和衍生物,在此将对它们进行讨论,重点强调寻找创新且更有效药物所面临的挑战。此外,我们将综述与新型拓扑异构酶相关治疗药物开发有关的新颖多样的方法。

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