Direct targeting of β-catenin: Inhibition of protein-protein interactions for the inactivation of Wnt signaling

被引:38
|
作者
Hahne, Gernot [1 ]
Grossmann, Tom N. [1 ]
机构
[1] Max Planck Gesell, Chem Genom Ctr, D-44227 Dortmund, Germany
关键词
beta-Catenin; Wnt signaling; Protein-protein interaction; Cancer; Transcription factor; SMALL-MOLECULE INHIBITORS; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; COMPLEX REVEALS; STAPLED P53; BH3; HELIX; BINDING; CANCER; APC; RECOGNITION;
D O I
10.1016/j.bmc.2013.02.050
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The activation of developmental signaling pathways such as Notch, Hedgehog and Wnt has implications in the onset and progression of numerous types of cancer. Consequently, targeting of such pathways is considered an attractive therapeutic approach. Inhibition of the Wnt signaling cascade proves to be complicated, in part, due to the lack of druggable pathway components. The central hub in Wnt signaling is the protein beta-catenin, which is involved in numerous protein-protein interactions. In general, the inhibition of protein-protein interactions is challenging in particular with binding interfaces lacking pronounced hydrophobic pockets. Herein, we give an overview of beta-catenin-protein interactions, and we review active agents that were reported to inhibit canonical Wnt signaling via direct targeting of beta-catenin. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4020 / 4026
页数:7
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