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Wnt signaling and colon carcinogenesis: Beyond APC

Activation of the Wnt signaling pathway via mutation of the adenomatous polyposis coli gene (APC) is a critical event in the development of colon cancer. For colon carcinogenesis, however, constitutive signaling through the canonical Wnt pathway is not a singular event. Here we review how canonical...

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Detalles Bibliográficos
Autores principales: Najdi, Rani, Holcombe, Randall F., Waterman, Marian L.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072659/
https://www.ncbi.nlm.nih.gov/pubmed/21483657
http://dx.doi.org/10.4103/1477-3163.78111
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author Najdi, Rani
Holcombe, Randall F.
Waterman, Marian L.
author_facet Najdi, Rani
Holcombe, Randall F.
Waterman, Marian L.
author_sort Najdi, Rani
collection PubMed
description Activation of the Wnt signaling pathway via mutation of the adenomatous polyposis coli gene (APC) is a critical event in the development of colon cancer. For colon carcinogenesis, however, constitutive signaling through the canonical Wnt pathway is not a singular event. Here we review how canonical Wnt signaling is modulated by intracellular LEF/TCF composition and location, the action of different Wnt ligands, and the secretion of Wnt inhibitory molecules. We also review the contributions of non-canonical Wnt signaling and other distinct pathways in the tumor micro environment that cross-talk to the canonical Wnt pathway and thereby influence colon cancer progression. These ‘non-APC’ aspects of Wnt signaling are considered in relation to the development of potential agents for the treatment of patients with colon cancer. Regulatory pathways that influence Wnt signaling highlight how it might be possible to design therapies that target a network of signals beyond that of APC and β-catenin.
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spelling pubmed-30726592011-04-11 Wnt signaling and colon carcinogenesis: Beyond APC Najdi, Rani Holcombe, Randall F. Waterman, Marian L. J Carcinog Review Article Activation of the Wnt signaling pathway via mutation of the adenomatous polyposis coli gene (APC) is a critical event in the development of colon cancer. For colon carcinogenesis, however, constitutive signaling through the canonical Wnt pathway is not a singular event. Here we review how canonical Wnt signaling is modulated by intracellular LEF/TCF composition and location, the action of different Wnt ligands, and the secretion of Wnt inhibitory molecules. We also review the contributions of non-canonical Wnt signaling and other distinct pathways in the tumor micro environment that cross-talk to the canonical Wnt pathway and thereby influence colon cancer progression. These ‘non-APC’ aspects of Wnt signaling are considered in relation to the development of potential agents for the treatment of patients with colon cancer. Regulatory pathways that influence Wnt signaling highlight how it might be possible to design therapies that target a network of signals beyond that of APC and β-catenin. Medknow Publications 2011-03-17 /pmc/articles/PMC3072659/ /pubmed/21483657 http://dx.doi.org/10.4103/1477-3163.78111 Text en © 2011 Najdi http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Najdi, Rani
Holcombe, Randall F.
Waterman, Marian L.
Wnt signaling and colon carcinogenesis: Beyond APC
title Wnt signaling and colon carcinogenesis: Beyond APC
title_full Wnt signaling and colon carcinogenesis: Beyond APC
title_fullStr Wnt signaling and colon carcinogenesis: Beyond APC
title_full_unstemmed Wnt signaling and colon carcinogenesis: Beyond APC
title_short Wnt signaling and colon carcinogenesis: Beyond APC
title_sort wnt signaling and colon carcinogenesis: beyond apc
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072659/
https://www.ncbi.nlm.nih.gov/pubmed/21483657
http://dx.doi.org/10.4103/1477-3163.78111
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