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Wnt/β-Catenin Signaling Pathway in Skin Carcinogenesis and Therapy

Cooperating with other signaling pathways, Wnt signaling controls cell proliferation, morphology, motility, and embryonic development destination and maintains the homeostasis of tissues including skin, blood, intestine, and brain by regulating somatic stem cells and their niches throughout adult li...

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Detalles Bibliográficos
Autores principales: Li, Jing, Ji, Ling, Chen, Jieping, Zhang, Wengeng, Ye, Zhijia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452418/
https://www.ncbi.nlm.nih.gov/pubmed/26078973
http://dx.doi.org/10.1155/2015/964842
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author Li, Jing
Ji, Ling
Chen, Jieping
Zhang, Wengeng
Ye, Zhijia
author_facet Li, Jing
Ji, Ling
Chen, Jieping
Zhang, Wengeng
Ye, Zhijia
author_sort Li, Jing
collection PubMed
description Cooperating with other signaling pathways, Wnt signaling controls cell proliferation, morphology, motility, and embryonic development destination and maintains the homeostasis of tissues including skin, blood, intestine, and brain by regulating somatic stem cells and their niches throughout adult life. Abnormal regulation of Wnt pathways leads to neoplastic proliferation in these tissues. Recent research shows that Wnt signaling is also associated with the regulation of cancer stem cells (CSCs) through a similar mechanism to that observed in normal adult stem cells. Thus, the Wnt/β-catenin signaling pathway has been intensively studied and characterized. For this review, we will focus on the regulation of the Wnt/β-catenin signaling pathway in skin cancer. With the important role in stemness and skin CSC proliferation, the Wnt/β-catenin signaling pathway and its elements have the potential to be targets for skin cancer therapy.
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spelling pubmed-44524182015-06-15 Wnt/β-Catenin Signaling Pathway in Skin Carcinogenesis and Therapy Li, Jing Ji, Ling Chen, Jieping Zhang, Wengeng Ye, Zhijia Biomed Res Int Review Article Cooperating with other signaling pathways, Wnt signaling controls cell proliferation, morphology, motility, and embryonic development destination and maintains the homeostasis of tissues including skin, blood, intestine, and brain by regulating somatic stem cells and their niches throughout adult life. Abnormal regulation of Wnt pathways leads to neoplastic proliferation in these tissues. Recent research shows that Wnt signaling is also associated with the regulation of cancer stem cells (CSCs) through a similar mechanism to that observed in normal adult stem cells. Thus, the Wnt/β-catenin signaling pathway has been intensively studied and characterized. For this review, we will focus on the regulation of the Wnt/β-catenin signaling pathway in skin cancer. With the important role in stemness and skin CSC proliferation, the Wnt/β-catenin signaling pathway and its elements have the potential to be targets for skin cancer therapy. Hindawi Publishing Corporation 2015 2015-05-19 /pmc/articles/PMC4452418/ /pubmed/26078973 http://dx.doi.org/10.1155/2015/964842 Text en Copyright © 2015 Jing Li et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Li, Jing
Ji, Ling
Chen, Jieping
Zhang, Wengeng
Ye, Zhijia
Wnt/β-Catenin Signaling Pathway in Skin Carcinogenesis and Therapy
title Wnt/β-Catenin Signaling Pathway in Skin Carcinogenesis and Therapy
title_full Wnt/β-Catenin Signaling Pathway in Skin Carcinogenesis and Therapy
title_fullStr Wnt/β-Catenin Signaling Pathway in Skin Carcinogenesis and Therapy
title_full_unstemmed Wnt/β-Catenin Signaling Pathway in Skin Carcinogenesis and Therapy
title_short Wnt/β-Catenin Signaling Pathway in Skin Carcinogenesis and Therapy
title_sort wnt/β-catenin signaling pathway in skin carcinogenesis and therapy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452418/
https://www.ncbi.nlm.nih.gov/pubmed/26078973
http://dx.doi.org/10.1155/2015/964842
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