β-Catenin and Theβ-Catenin Destruction Complex From Basic Science to Drug Design附视频

被引:0
|
作者
DAVID KIMELMAN
机构
[1] Department of Biochemistry
[2] University of Washington Seattle
[3] WA
[4] 不详
关键词
Wnt pathway; β-catenin; β-catenin destruction complex; APC; cancer; stem cell; intercellular signaling;
D O I
暂无
中图分类号
R914.2 [药物设计];
学科分类号
摘要
The canonical Wnt/β-catenin signaling pathway plays critical roles in both embryonic development and tumorigenesis. Central to the pathway is the turnover of β-catenin, a protein that functions in both cell adhesion and transcription. In the absence of a Wnt signal, free cytosolic β-catenin is phosphorylated by a large protein complex called the “β-catenin destruction complex” that targets β-catenin for degradation by an ubiquitin ligase/proteasome system. In the presence of a Wnt signal, the binding of Wnt to its receptor Frizzled and co-receptor LRP leads to the inhibition of β-catenin phosphorylation in the β-catenin destruction complex through an unknown mechanism. Inhibition of the β-catenin destruction complex leads to the accumulation of nuclear β-catenin, which in turn forms a complex with Tcf and BCL9. Recent studies have provided important clues regarding the molecular mechanism of the β-catenin destruction complex as well as an explanation for how β-catenin switches between its roles in cell adhesion and transcription.
引用
收藏
页码:903 / 911
页数:9
相关论文
共 1 条