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Notch signaling in glioblastoma: a developmental drug target?

Malignant gliomas are among the most devastating tumors for which conventional therapies have not significantly improved patient outcome. Despite advances in imaging, surgery, chemotherapy and radiotherapy, survival is still less than 2 years from diagnosis and more targeted therapies are urgently n...

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Detalles Bibliográficos
Autores principales: Lino, Maria Maddalena, Merlo, Adrian, Boulay, Jean-Louis
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996337/
https://www.ncbi.nlm.nih.gov/pubmed/21078177
http://dx.doi.org/10.1186/1741-7015-8-72
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author Lino, Maria Maddalena
Merlo, Adrian
Boulay, Jean-Louis
author_facet Lino, Maria Maddalena
Merlo, Adrian
Boulay, Jean-Louis
author_sort Lino, Maria Maddalena
collection PubMed
description Malignant gliomas are among the most devastating tumors for which conventional therapies have not significantly improved patient outcome. Despite advances in imaging, surgery, chemotherapy and radiotherapy, survival is still less than 2 years from diagnosis and more targeted therapies are urgently needed. Notch signaling is central to the normal and neoplastic development of the central nervous system, playing important roles in proliferation, differentiation, apoptosis and cancer stem cell regulation. Notch is also involved in the regulation response to hypoxia and angiogenesis, which are typical tumor and more specifically glioblastoma multiforme (GBM) features. Targeting Notch signaling is therefore a promising strategy for developing future therapies for the treatment of GBM. In this review we give an overview of the mechanisms of Notch signaling, its networking pathways in gliomas, and discuss its potential for designing novel therapeutic approaches.
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spelling pubmed-29963372010-12-03 Notch signaling in glioblastoma: a developmental drug target? Lino, Maria Maddalena Merlo, Adrian Boulay, Jean-Louis BMC Med Review Malignant gliomas are among the most devastating tumors for which conventional therapies have not significantly improved patient outcome. Despite advances in imaging, surgery, chemotherapy and radiotherapy, survival is still less than 2 years from diagnosis and more targeted therapies are urgently needed. Notch signaling is central to the normal and neoplastic development of the central nervous system, playing important roles in proliferation, differentiation, apoptosis and cancer stem cell regulation. Notch is also involved in the regulation response to hypoxia and angiogenesis, which are typical tumor and more specifically glioblastoma multiforme (GBM) features. Targeting Notch signaling is therefore a promising strategy for developing future therapies for the treatment of GBM. In this review we give an overview of the mechanisms of Notch signaling, its networking pathways in gliomas, and discuss its potential for designing novel therapeutic approaches. BioMed Central 2010-11-15 /pmc/articles/PMC2996337/ /pubmed/21078177 http://dx.doi.org/10.1186/1741-7015-8-72 Text en Copyright ©2010 Lino et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Lino, Maria Maddalena
Merlo, Adrian
Boulay, Jean-Louis
Notch signaling in glioblastoma: a developmental drug target?
title Notch signaling in glioblastoma: a developmental drug target?
title_full Notch signaling in glioblastoma: a developmental drug target?
title_fullStr Notch signaling in glioblastoma: a developmental drug target?
title_full_unstemmed Notch signaling in glioblastoma: a developmental drug target?
title_short Notch signaling in glioblastoma: a developmental drug target?
title_sort notch signaling in glioblastoma: a developmental drug target?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996337/
https://www.ncbi.nlm.nih.gov/pubmed/21078177
http://dx.doi.org/10.1186/1741-7015-8-72
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