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Current Therapeutic Advances Targeting EGFR and EGFRvIII in Glioblastoma

Epidermal growth factor receptor (EGFR) and EGFRvIII analysis is of current interest in glioblastoma – the most common malignant primary CNS tumor, because of new EGFRvIII vaccine trials underway. EGFR activation in glioblastoma promotes cellular proliferation via activation of MAPK and PI3K–Akt pat...

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Autores principales: Padfield, Emily, Ellis, Hayley P., Kurian, Kathreena M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310282/
https://www.ncbi.nlm.nih.gov/pubmed/25688333
http://dx.doi.org/10.3389/fonc.2015.00005
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author Padfield, Emily
Ellis, Hayley P.
Kurian, Kathreena M.
author_facet Padfield, Emily
Ellis, Hayley P.
Kurian, Kathreena M.
author_sort Padfield, Emily
collection PubMed
description Epidermal growth factor receptor (EGFR) and EGFRvIII analysis is of current interest in glioblastoma – the most common malignant primary CNS tumor, because of new EGFRvIII vaccine trials underway. EGFR activation in glioblastoma promotes cellular proliferation via activation of MAPK and PI3K–Akt pathways, and EGFRvIII is the most common variant, leading to constitutively active EGFR. This review explains EGFR and EGFRvIII signaling in GBM; describes targeted therapy approaches to date including tyrosine kinase inhibitor, antibody-based therapies, vaccines and pre-clinical RNA-based therapies, and discusses the difficulties encountered with these approaches including pathway redundancy and intratumoral heterogeneity.
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spelling pubmed-43102822015-02-16 Current Therapeutic Advances Targeting EGFR and EGFRvIII in Glioblastoma Padfield, Emily Ellis, Hayley P. Kurian, Kathreena M. Front Oncol Oncology Epidermal growth factor receptor (EGFR) and EGFRvIII analysis is of current interest in glioblastoma – the most common malignant primary CNS tumor, because of new EGFRvIII vaccine trials underway. EGFR activation in glioblastoma promotes cellular proliferation via activation of MAPK and PI3K–Akt pathways, and EGFRvIII is the most common variant, leading to constitutively active EGFR. This review explains EGFR and EGFRvIII signaling in GBM; describes targeted therapy approaches to date including tyrosine kinase inhibitor, antibody-based therapies, vaccines and pre-clinical RNA-based therapies, and discusses the difficulties encountered with these approaches including pathway redundancy and intratumoral heterogeneity. Frontiers Media S.A. 2015-01-29 /pmc/articles/PMC4310282/ /pubmed/25688333 http://dx.doi.org/10.3389/fonc.2015.00005 Text en Copyright © 2015 Padfield, Ellis and Kurian. 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 Oncology
Padfield, Emily
Ellis, Hayley P.
Kurian, Kathreena M.
Current Therapeutic Advances Targeting EGFR and EGFRvIII in Glioblastoma
title Current Therapeutic Advances Targeting EGFR and EGFRvIII in Glioblastoma
title_full Current Therapeutic Advances Targeting EGFR and EGFRvIII in Glioblastoma
title_fullStr Current Therapeutic Advances Targeting EGFR and EGFRvIII in Glioblastoma
title_full_unstemmed Current Therapeutic Advances Targeting EGFR and EGFRvIII in Glioblastoma
title_short Current Therapeutic Advances Targeting EGFR and EGFRvIII in Glioblastoma
title_sort current therapeutic advances targeting egfr and egfrviii in glioblastoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310282/
https://www.ncbi.nlm.nih.gov/pubmed/25688333
http://dx.doi.org/10.3389/fonc.2015.00005
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