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Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis

Neural crest (NC) cells are a temporary population of multipotent stem cells that generate a diverse array of cell types, including craniofacial bone and cartilage, smooth muscle cells, melanocytes, and peripheral neurons and glia during embryonic development. Defective neural crest development can...

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Detalles Bibliográficos
Autores principales: Ji, Yu, Hao, Hongyan, Reynolds, Kurt, McMahon, Moira, Zhou, Chengji J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829301/
https://www.ncbi.nlm.nih.gov/pubmed/31569501
http://dx.doi.org/10.3390/cells8101173
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author Ji, Yu
Hao, Hongyan
Reynolds, Kurt
McMahon, Moira
Zhou, Chengji J.
author_facet Ji, Yu
Hao, Hongyan
Reynolds, Kurt
McMahon, Moira
Zhou, Chengji J.
author_sort Ji, Yu
collection PubMed
description Neural crest (NC) cells are a temporary population of multipotent stem cells that generate a diverse array of cell types, including craniofacial bone and cartilage, smooth muscle cells, melanocytes, and peripheral neurons and glia during embryonic development. Defective neural crest development can cause severe and common structural birth defects, such as craniofacial anomalies and congenital heart disease. In the early vertebrate embryos, NC cells emerge from the dorsal edge of the neural tube during neurulation and then migrate extensively throughout the anterior-posterior body axis to generate numerous derivatives. Wnt signaling plays essential roles in embryonic development and cancer. This review summarizes current understanding of Wnt signaling in NC cell induction, delamination, migration, multipotency, and fate determination, as well as in NC-derived cancers.
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spelling pubmed-68293012019-11-18 Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis Ji, Yu Hao, Hongyan Reynolds, Kurt McMahon, Moira Zhou, Chengji J. Cells Review Neural crest (NC) cells are a temporary population of multipotent stem cells that generate a diverse array of cell types, including craniofacial bone and cartilage, smooth muscle cells, melanocytes, and peripheral neurons and glia during embryonic development. Defective neural crest development can cause severe and common structural birth defects, such as craniofacial anomalies and congenital heart disease. In the early vertebrate embryos, NC cells emerge from the dorsal edge of the neural tube during neurulation and then migrate extensively throughout the anterior-posterior body axis to generate numerous derivatives. Wnt signaling plays essential roles in embryonic development and cancer. This review summarizes current understanding of Wnt signaling in NC cell induction, delamination, migration, multipotency, and fate determination, as well as in NC-derived cancers. MDPI 2019-09-29 /pmc/articles/PMC6829301/ /pubmed/31569501 http://dx.doi.org/10.3390/cells8101173 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ji, Yu
Hao, Hongyan
Reynolds, Kurt
McMahon, Moira
Zhou, Chengji J.
Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis
title Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis
title_full Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis
title_fullStr Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis
title_full_unstemmed Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis
title_short Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis
title_sort wnt signaling in neural crest ontogenesis and oncogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829301/
https://www.ncbi.nlm.nih.gov/pubmed/31569501
http://dx.doi.org/10.3390/cells8101173
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