Wnt signaling pathway
From Proteopedia
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Three Wnt signaling pathways have been characterized: the canonical Wnt pathway, the noncanonical planar cell polarity pathway, and the noncanonical Wnt/calcium pathway. All three pathways are activated by the binding of a Wnt-protein ligand to a Frizzled family receptor, which passes the biological signal to the Dishevelled protein inside the cell. <scene name='90/909987/Cv/3'>Crystal structure of XWnt8 (green) in complex with the cysteine-rich domain of Frizzled 8 (deep sky blue)</scene> ([[4f0a]]). The canonical Wnt pathway leads to regulation of gene transcription, and is thought to be negatively regulated in part by the SPATS1 gene. The noncanonical planar cell polarity pathway regulates the cytoskeleton that is responsible for the shape of the cell. The noncanonical Wnt/calcium pathway regulates calcium inside the cell. | Three Wnt signaling pathways have been characterized: the canonical Wnt pathway, the noncanonical planar cell polarity pathway, and the noncanonical Wnt/calcium pathway. All three pathways are activated by the binding of a Wnt-protein ligand to a Frizzled family receptor, which passes the biological signal to the Dishevelled protein inside the cell. <scene name='90/909987/Cv/3'>Crystal structure of XWnt8 (green) in complex with the cysteine-rich domain of Frizzled 8 (deep sky blue)</scene> ([[4f0a]]). The canonical Wnt pathway leads to regulation of gene transcription, and is thought to be negatively regulated in part by the SPATS1 gene. The noncanonical planar cell polarity pathway regulates the cytoskeleton that is responsible for the shape of the cell. The noncanonical Wnt/calcium pathway regulates calcium inside the cell. | ||
+ | Normally, the [[Wnt signaling pathway]] leads to stabilization of β-catenin (see [[Catenin]]) through inactivation of a protein complex containing the tumor suppressors [[Adenomatous polyposis coli]] (APC) and [[Axin]]. Genetic alterations that lead to de-regulation of the autocrine Wnt pathway result in transactivation of [[Epidermal Growth Factor Receptor]] (EGFR) and other pathways, in turn contributing to proliferation of tumor cells. | ||
</StructureSection> | </StructureSection> | ||
== References == | == References == | ||
<references/> | <references/> |
Revision as of 14:01, 2 May 2022
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