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WNT signaling at the intersection between neurogenesis and brain tumorigenesis

Neurogenesis and tumorigenesis share signaling molecules/pathways involved in cell proliferation, differentiation, migration, and death. Self-renewal of neural stem cells is a tightly regulated process that secures the accuracy of cell division and eliminates cells that undergo mitotic errors. Abnor...

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Detalles Bibliográficos
Autores principales: Alkailani, Maisa I., Aittaleb, Mohamed, Tissir, Fadel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577257/
https://www.ncbi.nlm.nih.gov/pubmed/36267699
http://dx.doi.org/10.3389/fnmol.2022.1017568
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author Alkailani, Maisa I.
Aittaleb, Mohamed
Tissir, Fadel
author_facet Alkailani, Maisa I.
Aittaleb, Mohamed
Tissir, Fadel
author_sort Alkailani, Maisa I.
collection PubMed
description Neurogenesis and tumorigenesis share signaling molecules/pathways involved in cell proliferation, differentiation, migration, and death. Self-renewal of neural stem cells is a tightly regulated process that secures the accuracy of cell division and eliminates cells that undergo mitotic errors. Abnormalities in the molecular mechanisms controlling this process can trigger aneuploidy and genome instability, leading to neoplastic transformation. Mutations that affect cell adhesion, polarity, or migration enhance the invasive potential and favor the progression of tumors. Here, we review recent evidence of the WNT pathway’s involvement in both neurogenesis and tumorigenesis and discuss the experimental progress on therapeutic opportunities targeting components of this pathway.
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spelling pubmed-95772572022-10-19 WNT signaling at the intersection between neurogenesis and brain tumorigenesis Alkailani, Maisa I. Aittaleb, Mohamed Tissir, Fadel Front Mol Neurosci Molecular Neuroscience Neurogenesis and tumorigenesis share signaling molecules/pathways involved in cell proliferation, differentiation, migration, and death. Self-renewal of neural stem cells is a tightly regulated process that secures the accuracy of cell division and eliminates cells that undergo mitotic errors. Abnormalities in the molecular mechanisms controlling this process can trigger aneuploidy and genome instability, leading to neoplastic transformation. Mutations that affect cell adhesion, polarity, or migration enhance the invasive potential and favor the progression of tumors. Here, we review recent evidence of the WNT pathway’s involvement in both neurogenesis and tumorigenesis and discuss the experimental progress on therapeutic opportunities targeting components of this pathway. Frontiers Media S.A. 2022-10-04 /pmc/articles/PMC9577257/ /pubmed/36267699 http://dx.doi.org/10.3389/fnmol.2022.1017568 Text en Copyright © 2022 Alkailani, Aittaleb and Tissir. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Neuroscience
Alkailani, Maisa I.
Aittaleb, Mohamed
Tissir, Fadel
WNT signaling at the intersection between neurogenesis and brain tumorigenesis
title WNT signaling at the intersection between neurogenesis and brain tumorigenesis
title_full WNT signaling at the intersection between neurogenesis and brain tumorigenesis
title_fullStr WNT signaling at the intersection between neurogenesis and brain tumorigenesis
title_full_unstemmed WNT signaling at the intersection between neurogenesis and brain tumorigenesis
title_short WNT signaling at the intersection between neurogenesis and brain tumorigenesis
title_sort wnt signaling at the intersection between neurogenesis and brain tumorigenesis
topic Molecular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577257/
https://www.ncbi.nlm.nih.gov/pubmed/36267699
http://dx.doi.org/10.3389/fnmol.2022.1017568
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