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β-连环蛋白降解复合物的分子调控与药理学靶向。

Molecular regulation and pharmacological targeting of the β-catenin destruction complex.

机构信息

Department of Cell Biology, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

Br J Pharmacol. 2017 Dec;174(24):4575-4588. doi: 10.1111/bph.13922. Epub 2017 Aug 11.

Abstract

UNLABELLED

The β-catenin destruction complex is a dynamic cytosolic multiprotein assembly that provides a key node in Wnt signalling regulation. The core components of the destruction complex comprise the scaffold proteins axin and adenomatous polyposis coli and the Ser/Thr kinases casein kinase 1 and glycogen synthase kinase 3. In unstimulated cells, the destruction complex efficiently drives degradation of the transcriptional coactivator β-catenin, thereby preventing the activation of the Wnt/β-catenin pathway. Mutational inactivation of the destruction complex is a major pathway in the pathogenesis of cancer. Here, we review recent insights in the regulation of the β-catenin destruction complex, including newly identified interaction interfaces, regulatory elements and post-translationally controlled mechanisms. In addition, we discuss how mutations in core destruction complex components deregulate Wnt signalling via distinct mechanisms and how these findings open up potential therapeutic approaches to restore destruction complex activity in cancer cells.

LINKED ARTICLES

This article is part of a themed section on WNT Signalling: Mechanisms and Therapeutic Opportunities. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.24/issuetoc.

摘要

未标记

β-连环蛋白破坏复合物是一种动态的细胞溶质多蛋白组装体,提供了 Wnt 信号调节的关键节点。破坏复合物的核心组件包括支架蛋白轴蛋白和腺瘤性结肠息肉病和丝氨酸/苏氨酸激酶酪蛋白激酶 1 和糖原合酶激酶 3。在未受刺激的细胞中,破坏复合物有效地驱动转录共激活因子β-连环蛋白的降解,从而防止 Wnt/β-连环蛋白途径的激活。破坏复合物的突变失活是癌症发病机制中的主要途径。在这里,我们回顾了β-连环蛋白破坏复合物调节的最新见解,包括新发现的相互作用界面、调节元件和翻译后控制机制。此外,我们还讨论了核心破坏复合物成分中的突变如何通过不同的机制来调节 Wnt 信号,并讨论了这些发现如何为恢复癌细胞中破坏复合物的活性提供潜在的治疗方法。

链接文章

本文是 Wnt 信号:机制和治疗机会专题的一部分。要查看该部分中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.24/issuetoc.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5791/5727331/04e5dfb434bd/BPH-174-4575-g001.jpg

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