针对NACK atp酶的notch介导转录的新化学攻击。

IF 5.3 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Molecular Therapy Oncolytics Pub Date : 2023-03-16 DOI:10.1016/j.omto.2023.02.008
Giulia Diluvio, Tanya T Kelley, Mohini Lahiry, Annamil Alvarez-Trotta, Ellen M Kolb, Elena Shersher, Luisana Astudillo, Rhett A Kovall, Stephan C Schürer, Anthony J Capobianco
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引用次数: 1

摘要

Notch激活复合体激酶(NACK)是Notch转录机制的一个组成部分,对Notch介导的肿瘤发生至关重要。然而,NACK调控notch介导的转录的机制尚不清楚。在这里,我们证明了NACK结合并水解ATP,并且只有ATP结合的NACK才能与Notch三元配合物(NTC)结合。考虑到这一点,我们试图确定这种atp依赖功能的抑制剂,并使用计算管道发现了NACK的第一个小分子抑制剂Z271-0326,它直接阻断notch介导的转录活性,并在PDX小鼠模型中显示出有效的抗肿瘤活性。总之,我们已经发现了第一个通过阻断NTC下游的Notch活性来有效治疗Notch驱动型癌症的抑制剂。
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A novel chemical attack on Notch-mediated transcription by targeting the NACK ATPase.

Notch activation complex kinase (NACK) is a component of the Notch transcriptional machinery critical for the Notch-mediated tumorigenesis. However, the mechanism through which NACK regulates Notch-mediated transcription is not well understood. Here, we demonstrate that NACK binds and hydrolyzes ATP and that only ATP-bound NACK can bind to the Notch ternary complex (NTC). Considering this, we sought to identify inhibitors of this ATP-dependent function and, using computational pipelines, discovered the first small-molecule inhibitor of NACK, Z271-0326, that directly blocks the activity of Notch-mediated transcription and shows potent antineoplastic activity in PDX mouse models. In conclusion, we have discovered the first inhibitor that holds promise for the efficacious treatment of Notch-driven cancers by blocking the Notch activity downstream of the NTC.

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来源期刊
Molecular Therapy Oncolytics
Molecular Therapy Oncolytics Medicine-Oncology
CiteScore
10.90
自引率
3.50%
发文量
152
审稿时长
6 weeks
期刊介绍: Molecular Therapy — Oncolytics is an international, online-only, open access journal focusing on the development and clinical testing of viral, cellular, and other biological therapies targeting cancer.
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