Targeting TAK1: Evolution of inhibitors, challenges, and future directions

IF 12 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Nika Strašek Benedik , Matic Proj , Christian Steinebach , Matej Sova , Izidor Sosič
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引用次数: 0

Abstract

The increasing incidence of inflammatory and malignant diseases signifies the need to develop first-in-class drugs with novel mechanisms of action. In this respect, the transforming growth factor (TGF)-β-activated kinase 1 (TAK1), an essential part of several signaling pathways, is considered relevant and promising. This manuscript provides a brief overview of the signal transduction orchestrated by TAK1 within these pathways, followed by an in-depth and thorough analysis of the chemical matter demonstrated to inhibit this kinase. Special attention is given to the selectivity profiling of inhibitors, as well as to the outcomes of their biological characterization. Because published TAK1 inhibitors differ significantly in their kinome selectivity, active-site binding, and biological activity, we hope that this review will allow a judicial estimation of their quality and usefulness for TAK1-addressing assays. Our thoughts on the perspectives and possible developments of the field are also provided to assist scientists who are involved in the design and development of TAK1-targeting modulators.
靶向TAK1:抑制剂的发展、挑战和未来方向。
炎症和恶性疾病的发病率不断增加,这意味着需要开发具有新型作用机制的一流药物。在这方面,转化生长因子(TGF)-β-活化激酶1 (TAK1)作为几个信号通路的重要组成部分,被认为是相关的和有前途的。本文简要概述了TAK1在这些途径中的信号转导,然后对抑制这种激酶的化学物质进行了深入和彻底的分析。特别注意抑制剂的选择性分析,以及其生物学表征的结果。由于已发表的TAK1抑制剂在其激酶体选择性、活性位点结合和生物活性方面存在显著差异,我们希望这篇综述将允许对它们的质量和对TAK1定位测定的有用性进行公正的评估。我们对该领域的观点和可能的发展的想法也提供给参与tak1靶向调节剂的设计和开发的科学家。
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来源期刊
CiteScore
23.00
自引率
0.70%
发文量
222
审稿时长
90 days
期刊介绍: Pharmacology & Therapeutics, in its 20th year, delivers lucid, critical, and authoritative reviews on current pharmacological topics.Articles, commissioned by the editor, follow specific author instructions.This journal maintains its scientific excellence and ranks among the top 10 most cited journals in pharmacology.
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