The Wnt signaling pathway in development and disease

被引:4148
|
作者
Logan, CY [1 ]
Nusse, R [1 ]
机构
[1] Stanford Univ, Howard Hughes Med Inst, Beckman Ctr, Dept Dev Biol, Stanford, CA 94305 USA
关键词
embryogenesis; cancer; beta-catenin; Frizzled; stem cells;
D O I
10.1146/annurev.cellbio.20.010403.113126
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tight control of cell-cell communication is essential for the generation of a normally patterned embryo. A critical mediator of key cell-cell signaling events during embryogenesis is the highly conserved Wnt family of secreted proteins. Recent biochemical and genetic analyses have greatly enriched our understanding of how Wnts signal, and the list of canonical Wnt signaling components has exploded. The data reveal that multiple extracellular, cytoplasmic, and nuclear regulators intricately modulate Wnt signaling levels. In addition, receptor-ligand specificity and feedback loops help to determine Wnt signaling outputs. Writs are required for adult tissue maintenance, and perturbations in Wnt signaling promote both human degenerative diseases and cancer. The next few years are likely to see novel therapeutic reagents aimed at controlling Wnt signaling in order to alleviate these conditions.
引用
收藏
页码:781 / 810
页数:30
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