Regulation of Wnt signaling by protocadherins

被引:21
|
作者
Mah, Kar Men [1 ]
Weiner, Joshua A. [1 ,2 ,3 ]
机构
[1] Univ Iowa, Dept Biol, 143 Biol Bldg, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Psychiat, Iowa City, IA 52242 USA
[3] Univ Iowa, Iowa Neurosci Inst, Iowa City, IA 52242 USA
关键词
Planar cell polarity; Cell adhesion; Cancer; Tumor suppressor; Epigeneticsextra cellular cadherin (EC); CANDIDATE TUMOR-SUPPRESSOR; PLANAR CELL POLARITY; XENOPUS PARAXIAL PROTOCADHERIN; METHYLATION PROFILING REVEALS; TRANSCRIPTION FACTOR NFAT1; MAMMARY ONCOGENE INT-1; TYROSINE KINASE ROR2; NEURAL-TUBE DEFECTS; WNT/BETA-CATENIN; BETA-CATENIN;
D O I
10.1016/j.semcdb.2017.07.043
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The similar to 70 protocadherins comprise the largest group within the cadherin superfamily. Their diversity, the complexity of the mechanisms through which their genes are regulated, and their many critical functions in nervous system development have engendered a growing interest in elucidating the intracellular signaling pathways through which they act. Recently, multiple protocadherins across several subfamilies have been implicated as modulators of Wnt signaling pathways, and through this as potential tumor suppressors. Here, we review the extant data on the regulation by protocadherins of Wnt signaling pathways and components, and highlight some key unanswered questions that could shape future research. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:158 / 171
页数:14
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