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光活化光笼 UNC2025 用于触发膀胱癌中的 TAM 激酶抑制。

Light-Activatable Photocaged UNC2025 for Triggering TAM Kinase Inhibition in Bladder Cancer.

机构信息

Institut Curie, Université PSL CNRS UMR9187, Inserm U119, 91400, Orsay, France.

Université Paris-Saclay CNRS UMR9187, Inserm U119, 91400, Orsay, France.

出版信息

Chembiochem. 2024 Apr 16;25(8):e202300855. doi: 10.1002/cbic.202300855. Epub 2024 Mar 18.

DOI:10.1002/cbic.202300855
PMID:38363151
Abstract

Photopharmacology is an emerging field that utilizes photo-responsive molecules to enable control over the activity of a drug using light. The aim is to limit the therapeutic action of a drug at the level of diseased tissues and organs. Considering the well-known implications of protein kinases in cancer and the therapeutic issues associated with protein kinase inhibitors, the photopharmacology is seen as an innovative and alternative solution with great potential in oncology. In this context, we developed the first photocaged TAM kinase inhibitors based on UNC2025, a first-in-class small molecule kinase inhibitor. These prodrugs showed good stability in biologically relevant buffer and rapid photorelease of the photoremovable protecting group upon UV-light irradiation (<10 min.). These light-activatable prodrugs led to a 16-fold decrease to a complete loss of kinase inhibition, depending on the protein and the position at which the coumarin-type phototrigger was introduced. The most promising candidate was the N,O-dicaged compound, showing the superiority of having two photolabile protecting groups on UNC2025 for being entirely inactive on TAM kinases. Under UV-light irradiation, the N,O-dicaged compound recovered its inhibitory potency in enzymatic assays and displayed excellent antiproliferative activity in RT112 cell lines.

摘要

光药理学是一个新兴领域,它利用光响应分子来控制药物的活性。其目的是将药物的治疗作用局限在病变组织和器官的水平。鉴于蛋白激酶在癌症中的重要作用以及蛋白激酶抑制剂相关的治疗问题,光药理学被视为一种具有创新性和替代性的解决方案,在肿瘤学领域具有巨大的潜力。在这方面,我们基于 UNC2025 开发了第一批光笼型 TAM 激酶抑制剂,UNC2025 是一种首创的小分子激酶抑制剂。这些前药在生物学相关缓冲液中表现出良好的稳定性,并在紫外光照射下迅速释放光解保护基团(<10 分钟)。这些光激活前药导致激酶抑制作用降低 16 倍至完全丧失,具体取决于蛋白质和引入香豆素型光触发的位置。最有前途的候选物是 N,O-双笼化合物,它具有 UNC2025 上的两个光不稳定保护基团,对 TAM 激酶完全没有活性,显示出优越性。在紫外光照射下,N,O-双笼化合物在酶促测定中恢复了其抑制活性,并在 RT112 细胞系中表现出优异的抗增殖活性。

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