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Targeting WNT Signaling for Multifaceted Glioblastoma Therapy
The WNT signaling pathway has been of great interest to developmental biologists for decades and has more recently become a central topic for study in cancer biology. It is vital for cell growth and regulation of embryogenesis in many organ systems, particularly the CNS and its associated vasculatur...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645527/ https://www.ncbi.nlm.nih.gov/pubmed/29081735 http://dx.doi.org/10.3389/fncel.2017.00318 |
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author | McCord, Matthew Mukouyama, Yoh-suke Gilbert, Mark R. Jackson, Sadhana |
author_facet | McCord, Matthew Mukouyama, Yoh-suke Gilbert, Mark R. Jackson, Sadhana |
author_sort | McCord, Matthew |
collection | PubMed |
description | The WNT signaling pathway has been of great interest to developmental biologists for decades and has more recently become a central topic for study in cancer biology. It is vital for cell growth and regulation of embryogenesis in many organ systems, particularly the CNS and its associated vasculature. We summarize the role of WNT in CNS development and describe how WNT signaling makes key contributions to malignant glioma stemness, invasiveness, therapeutic resistance, and angiogenesis. The role of WNT in these mechanisms, along with creation and maintainance of the blood-brain barrier (BBB), points to the potential of WNT as a multi-faceted target in malignant glioma therapy. |
format | Online Article Text |
id | pubmed-5645527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56455272017-10-27 Targeting WNT Signaling for Multifaceted Glioblastoma Therapy McCord, Matthew Mukouyama, Yoh-suke Gilbert, Mark R. Jackson, Sadhana Front Cell Neurosci Neuroscience The WNT signaling pathway has been of great interest to developmental biologists for decades and has more recently become a central topic for study in cancer biology. It is vital for cell growth and regulation of embryogenesis in many organ systems, particularly the CNS and its associated vasculature. We summarize the role of WNT in CNS development and describe how WNT signaling makes key contributions to malignant glioma stemness, invasiveness, therapeutic resistance, and angiogenesis. The role of WNT in these mechanisms, along with creation and maintainance of the blood-brain barrier (BBB), points to the potential of WNT as a multi-faceted target in malignant glioma therapy. Frontiers Media S.A. 2017-10-13 /pmc/articles/PMC5645527/ /pubmed/29081735 http://dx.doi.org/10.3389/fncel.2017.00318 Text en Copyright © 2017 McCord, Mukouyama, Gilbert and Jackson. http://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) or licensor 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 | Neuroscience McCord, Matthew Mukouyama, Yoh-suke Gilbert, Mark R. Jackson, Sadhana Targeting WNT Signaling for Multifaceted Glioblastoma Therapy |
title | Targeting WNT Signaling for Multifaceted Glioblastoma Therapy |
title_full | Targeting WNT Signaling for Multifaceted Glioblastoma Therapy |
title_fullStr | Targeting WNT Signaling for Multifaceted Glioblastoma Therapy |
title_full_unstemmed | Targeting WNT Signaling for Multifaceted Glioblastoma Therapy |
title_short | Targeting WNT Signaling for Multifaceted Glioblastoma Therapy |
title_sort | targeting wnt signaling for multifaceted glioblastoma therapy |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645527/ https://www.ncbi.nlm.nih.gov/pubmed/29081735 http://dx.doi.org/10.3389/fncel.2017.00318 |
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