An emerging role for Wnt and GSK3 signaling pathways in schizophrenia

被引:42
|
作者
Singh, K. K. [1 ]
机构
[1] McMaster Univ, Dept Biochem & Biomed Sci, Stem Cell & Canc Res Inst, Hamilton, ON L8S 4K1, Canada
关键词
brain development; genetics; schizophrenia; wnt signaling; BETA-CATENIN; BEHAVIORAL PHENOTYPES; SOCIAL-INTERACTION; LITHIUM ACTION; INCREASE RISK; MICE; DISC1; ABNORMALITIES; BRAIN; MICRODELETIONS;
D O I
10.1111/cge.12111
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Singh KK. An emerging role for Wnt and GSK3 signaling pathways in schizophrenia. Clin Genet 2013: 83: 511-517. (C) John Wiley & Sons A/S. Published by Blackwell Publishing Ltd, 2013 Schizophrenia is a disabling illness with limited treatment options. The underlying pathophysiology remains unknown, partially due to its heterogeneous nature, and a lack of understanding of the biological functions of genetic risk factors. Several signaling pathways have been implicated, however, with the varying degrees of support. In this article, I will focus on the converging evidence supporting a prominent role for Wnt and glycogen synthase kinase 3 (GSK3) signaling in the biological bases of schizophrenia. This includes current pharmacological therapies that target GSK3, animal model and cell-based studies, and recent human genetic findings that implicate Wnt and GSK3 signaling.
引用
收藏
页码:511 / 517
页数:7
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