靶向转录因子的小分子方法

Huarui Cui, Morgan Stilgenbauer, Angela N. Koehler
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引用次数: 0

摘要

转录因子活性失调是各种癌症类型的显著特征。因此,以致癌转录依赖性为靶点作为一种潜在的治疗方法一直受到人们的关注。然而,由于转录因子的结构高度紊乱且缺乏明确的结合口袋,它们历来被认为是不可药用的靶点。尽管如此,近年来人们对其药理抑制和破坏的兴趣并未减弱。在此,我们将讨论针对各种转录因子的基于小分子的新方法。具有不同作用机制的配体,如抑制剂、分子胶降解剂和蛋白水解靶向嵌合体,最近在临床前和临床上都取得了成功。我们将回顾这些策略是如何克服靶向转录因子所带来的挑战的。《癌症生物学年度综述》第8卷的最终在线出版日期预计为2024年4月。修订后的预计日期请参见 http://www.annualreviews.org/page/journal/pubdates。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Small-Molecule Approaches to Target Transcription Factors
Dysregulated transcription factor activity is a defining feature of various cancer types. As such, targeting oncogenic transcriptional dependency has long been pursued as a potential therapeutic approach. However, transcription factors have historically been deemed as undruggable targets due to their highly disordered structures and lack of well-defined binding pockets. Nevertheless, interest in their pharmacologic inhibition and destruction has not dwindled in recent years. Here, we discuss new small-molecule-based approaches to target various transcription factors. Ligands with different mechanisms of action, such as inhibitors, molecular glue degraders, and proteolysis targeting chimeras, have recently seen success preclinically and clinically. We review how these strategies overcome the challenges presented by targeting transcription factors.Expected final online publication date for the Annual Review of Cancer Biology, Volume 8 is April 2024. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.
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