College of Pharmacy, School of Medicine, Hangzhou Normal University, Hangzhou, Zhejiang Province, Zhejiang, People's Republic of China.
Engineering Laboratory of Development and Application of Traditional Chinese Medicine from Zhejiang Province, Zhejiang Province, People's Republic of China.
Expert Opin Ther Pat. 2021 May;31(5):435-452. doi: 10.1080/13543776.2021.1866540. Epub 2021 Feb 10.
: DNA-dependent protein kinase (DNA-PK) plays a crucial role in the repair of DSBs via non-homologous end joining (NHEJ). Several DNA-PK inhibitors are being investigated for potential anticancer treatment in clinical trials.: This review aims to give an overview of patents published since 2010 by analyzing the patent space and structure features of scaffolds used in those patents. It also discusses the recent clinical developments and provides perspectives on future challenges and directions in this field.: As a key component of the DNA damage response (DDR) pathway, DNA-PK appears to be a viable drug target for anticancer therapy. The clinical investigation of a DNA-PK inhibitor employs both a monotherapy and a combination strategy. In the combination strategy, a DNA-PK inhibitor is typically combined with a DSB inducer, radiation, a chemotherapy agent, or a PARP inhibitor, etc. Patent analyses suggest that diverse structures comprising different scaffolds from mono-heteroaryl to bicyclic heteroaryl to tricyclic heteroaryl are capable to achieve good DNA-PK inhibitory activity and good DNA-PK selectivity over other closely related enzymes. Several DNA-PK inhibitors are currently being evaluated in clinics, with the hope to get approval in the near future.
: DNA 依赖性蛋白激酶 (DNA-PK) 通过非同源末端连接 (NHEJ) 在双链断裂 (DSB) 的修复中发挥关键作用。目前正在临床试验中研究几种 DNA-PK 抑制剂,以作为潜在的抗癌治疗方法。
: 本综述旨在通过分析自 2010 年以来公布的专利,概述专利空间和这些专利中使用的支架的结构特征。还讨论了最近的临床进展,并对该领域未来的挑战和方向提供了展望。
: DNA-PK 作为 DNA 损伤反应 (DDR) 途径的关键组成部分,似乎是抗癌治疗的一个可行的药物靶点。DNA-PK 抑制剂的临床研究采用单药治疗和联合治疗策略。在联合治疗策略中,DNA-PK 抑制剂通常与 DSB 诱导剂、辐射、化疗药物或 PARP 抑制剂等联合使用。专利分析表明,包含从单杂芳基到双环杂芳基到三环杂芳基等不同支架的多种结构能够实现良好的 DNA-PK 抑制活性和对其他密切相关酶的良好 DNA-PK 选择性。目前正在临床评估几种 DNA-PK 抑制剂,希望在不久的将来获得批准。