Literature DB >> 10647780

Modulation of Wnt signaling by Axin and Axil.

A Kikuchi1.   

Abstract

The Wnt signaling pathway is conserved in various species from worms to mammals, and plays important roles in development, cellular proliferation, and differentiation. The molecular mechanisms by which the Wnt signal regulates cellular functions are becoming increasingly well understood. Wnt stabilizes cytoplasmic beta-catenin, which stimulates the expression of genes including c-myc, c-jun, fra-1, and cyclin D1. Axin and its homolog Axil, newly recognized as components of the Wnt signaling pathway, negatively regulate this pathway. Other components of the Wnt signaling pathway, including Dvl, glycogen synthase kinase-3beta (GSK-3beta), beta-catenin, and adenomatous polyposis coli (APC), interact with Axin, and the phosphorylation and stability of beta-catenin are regulated in the Axin complex. Axil has similar functions to Axin. Thus, Axin and Axil act as scaffold proteins in the Wnt signaling pathway, thereby modulating the Wnt-dependent cellular functions.

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Year:  1999        PMID: 10647780     DOI: 10.1016/s1359-6101(99)00017-9

Source DB:  PubMed          Journal:  Cytokine Growth Factor Rev        ISSN: 1359-6101            Impact factor:   7.638


  23 in total

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4.  Genetic and epigenetic changes of components affecting the WNT pathway in colorectal carcinomas stratified by microsatellite instability.

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Review 5.  GSK3 takes centre stage more than 20 years after its discovery.

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Authors:  R Tavares; J Vidal; A van Lammeren; M Kreis
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8.  Initiation of Wnt signaling: control of Wnt coreceptor Lrp6 phosphorylation/activation via frizzled, dishevelled and axin functions.

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Journal:  Development       Date:  2007-12-12       Impact factor: 6.868

9.  Changes of AXIN-1 and beta-catenin in neuroepithelial brain tumors.

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Journal:  Pathol Oncol Res       Date:  2009-07-25       Impact factor: 3.201

10.  Mutations in components of the Wnt signaling pathway in gastric cancer.

Authors:  Kai-Feng Pan; Wan-Guo Liu; Lian Zhang; Wei-Cheng You; You-Yong Lu
Journal:  World J Gastroenterol       Date:  2008-03-14       Impact factor: 5.742

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