The Wnt pathway and the roles for its antagonists, DKKS, in angiogenesis

被引:102
作者
Choi, Hyun-Jung [1 ]
Park, Hongryeol [1 ]
Lee, Heon-Woo [1 ]
Kwon, Young-Guen [1 ]
机构
[1] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biochem, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
Wnt; Dkk; endothelial cells; angiogenesis; signaling; TYROSINE KINASE ROR2; FAMILIAL EXUDATIVE VITREORETINOPATHY; ENDOTHELIAL-CELL PROLIFERATION; FRIZZLED-RELATED PROTEIN; BETA-CATENIN; SIGNALING PATHWAY; VASCULAR DEVELOPMENT; NEGATIVE REGULATION; DICKKOPF PROTEINS; AXON GUIDANCE;
D O I
10.1002/iub.1062
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The Wnt signaling pathway is involved in a wide range of developmental and physiological processes, such as cell fate specification, tissue morphogenesis, and homeostasis. Thus, its dysregulation has been found in multiple diseases, including some cardiovascular disorders. The loss or gain of function of Wnt pathway components results in abnormal vascular development and angiogenesis. Further study has revealed that Wnt signaling in endothelial cells appears to contribute to vascular morphogenesis and endothelial cell specification. Owing to the significance of Wnt signaling in angiogenesis, Wnt antagonists have been considered potential treatments for neovascular disorders. In line with this, members of the Dkk protein family (Dkks), well-known Wnt antagonists, have been recently found to regulate angiogenesis. This review summarizes our present knowledge of the roles of Wnt signaling and Wnt antagonists, particularly Dkks, in angiogenic regulation and explores the therapeutic potential of Wnt antagonists. (c) 2012 IUBMB IUBMB Life, 64(9): 724731, 2012
引用
收藏
页码:724 / 731
页数:8
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