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Role of the Wnt Pathway in Thyroid Cancer

Aberrant activation of Wnt signaling is involved in the development of several epithelial tumors. Wnt signaling includes two major types of pathways: (i) the canonical or Wnt/β-catenin pathway; and (ii) the non-canonical pathways, which do not involve β-catenin stabilization. Among these pathways, t...

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Autores principales: Sastre-Perona, Ana, Santisteban, Pilar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355838/
https://www.ncbi.nlm.nih.gov/pubmed/22645520
http://dx.doi.org/10.3389/fendo.2012.00031
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author Sastre-Perona, Ana
Santisteban, Pilar
author_facet Sastre-Perona, Ana
Santisteban, Pilar
author_sort Sastre-Perona, Ana
collection PubMed
description Aberrant activation of Wnt signaling is involved in the development of several epithelial tumors. Wnt signaling includes two major types of pathways: (i) the canonical or Wnt/β-catenin pathway; and (ii) the non-canonical pathways, which do not involve β-catenin stabilization. Among these pathways, the Wnt/β-catenin pathway has received most attention during the past years for its critical role in cancer. A number of publications emphasize the role of the Wnt/β-catenin pathway in thyroid cancer. This pathway plays a crucial role in development and epithelial renewal, and components such as β-catenin and Axin are often mutated in thyroid cancer. Although it is accepted that altered Wnt signaling is a late event in thyroid cell transformation that affects anaplastic thyroid tumors, recent data suggest that it is also altered in papillary thyroid carcinoma (PTC) with RET/PTC mutations. Therefore, the purpose of this review is to summarize the main relevant data of Wnt signaling in thyroid cancer, with special emphasis on the Wnt/β-catenin pathway.
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spelling pubmed-33558382012-05-29 Role of the Wnt Pathway in Thyroid Cancer Sastre-Perona, Ana Santisteban, Pilar Front Endocrinol (Lausanne) Endocrinology Aberrant activation of Wnt signaling is involved in the development of several epithelial tumors. Wnt signaling includes two major types of pathways: (i) the canonical or Wnt/β-catenin pathway; and (ii) the non-canonical pathways, which do not involve β-catenin stabilization. Among these pathways, the Wnt/β-catenin pathway has received most attention during the past years for its critical role in cancer. A number of publications emphasize the role of the Wnt/β-catenin pathway in thyroid cancer. This pathway plays a crucial role in development and epithelial renewal, and components such as β-catenin and Axin are often mutated in thyroid cancer. Although it is accepted that altered Wnt signaling is a late event in thyroid cell transformation that affects anaplastic thyroid tumors, recent data suggest that it is also altered in papillary thyroid carcinoma (PTC) with RET/PTC mutations. Therefore, the purpose of this review is to summarize the main relevant data of Wnt signaling in thyroid cancer, with special emphasis on the Wnt/β-catenin pathway. Frontiers Research Foundation 2012-02-29 /pmc/articles/PMC3355838/ /pubmed/22645520 http://dx.doi.org/10.3389/fendo.2012.00031 Text en Copyright © 2012 Sastre-Perona and Santisteban. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Endocrinology
Sastre-Perona, Ana
Santisteban, Pilar
Role of the Wnt Pathway in Thyroid Cancer
title Role of the Wnt Pathway in Thyroid Cancer
title_full Role of the Wnt Pathway in Thyroid Cancer
title_fullStr Role of the Wnt Pathway in Thyroid Cancer
title_full_unstemmed Role of the Wnt Pathway in Thyroid Cancer
title_short Role of the Wnt Pathway in Thyroid Cancer
title_sort role of the wnt pathway in thyroid cancer
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355838/
https://www.ncbi.nlm.nih.gov/pubmed/22645520
http://dx.doi.org/10.3389/fendo.2012.00031
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