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EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma
The EphA3 receptor has recently emerged as a functional tumour-specific therapeutic target in glioblastoma (GBM). EphA3 is significantly elevated in recurrent disease, is most highly expressed on glioma stem cells (GSCs), and has a functional role in maintaining self-renewal and tumourigenesis. An u...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316644/ https://www.ncbi.nlm.nih.gov/pubmed/30562956 http://dx.doi.org/10.3390/cancers10120519 |
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author | Offenhäuser, Carolin Al-Ejeh, Fares Puttick, Simon Ensbey, Kathleen S. Bruce, Zara C. Jamieson, Paul R. Smith, Fiona M. Stringer, Brett W. Carrington, Benjamin Fuchs, Adrian V. Bell, Craig A. Jeffree, Rosalind Rose, Stephen Thurecht, Kristofer J. Boyd, Andrew W. Day, Bryan W. |
author_facet | Offenhäuser, Carolin Al-Ejeh, Fares Puttick, Simon Ensbey, Kathleen S. Bruce, Zara C. Jamieson, Paul R. Smith, Fiona M. Stringer, Brett W. Carrington, Benjamin Fuchs, Adrian V. Bell, Craig A. Jeffree, Rosalind Rose, Stephen Thurecht, Kristofer J. Boyd, Andrew W. Day, Bryan W. |
author_sort | Offenhäuser, Carolin |
collection | PubMed |
description | The EphA3 receptor has recently emerged as a functional tumour-specific therapeutic target in glioblastoma (GBM). EphA3 is significantly elevated in recurrent disease, is most highly expressed on glioma stem cells (GSCs), and has a functional role in maintaining self-renewal and tumourigenesis. An unlabelled EphA3-targeting therapeutic antibody is currently under clinical assessment in recurrent GBM patients. In this study, we assessed the efficacy of EphA3 antibody drug conjugate (ADC) and radioimmunotherapy (RIT) approaches using orthotopic animal xenograft models. Brain uptake studies, using positron emission tomography/computed tomography (PET/CT) imaging, show EphA3 antibodies are effectively delivered across the blood-tumour barrier and accumulate at the tumour site with no observed normal brain reactivity. A robust anti-tumour response, with no toxicity, was observed using EphA3, ADC, and RIT approaches, leading to a significant increase in overall survival. Our current research provides evidence that GBM patients may benefit from pay-loaded EphA3 antibody therapies. |
format | Online Article Text |
id | pubmed-6316644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63166442019-01-09 EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma Offenhäuser, Carolin Al-Ejeh, Fares Puttick, Simon Ensbey, Kathleen S. Bruce, Zara C. Jamieson, Paul R. Smith, Fiona M. Stringer, Brett W. Carrington, Benjamin Fuchs, Adrian V. Bell, Craig A. Jeffree, Rosalind Rose, Stephen Thurecht, Kristofer J. Boyd, Andrew W. Day, Bryan W. Cancers (Basel) Article The EphA3 receptor has recently emerged as a functional tumour-specific therapeutic target in glioblastoma (GBM). EphA3 is significantly elevated in recurrent disease, is most highly expressed on glioma stem cells (GSCs), and has a functional role in maintaining self-renewal and tumourigenesis. An unlabelled EphA3-targeting therapeutic antibody is currently under clinical assessment in recurrent GBM patients. In this study, we assessed the efficacy of EphA3 antibody drug conjugate (ADC) and radioimmunotherapy (RIT) approaches using orthotopic animal xenograft models. Brain uptake studies, using positron emission tomography/computed tomography (PET/CT) imaging, show EphA3 antibodies are effectively delivered across the blood-tumour barrier and accumulate at the tumour site with no observed normal brain reactivity. A robust anti-tumour response, with no toxicity, was observed using EphA3, ADC, and RIT approaches, leading to a significant increase in overall survival. Our current research provides evidence that GBM patients may benefit from pay-loaded EphA3 antibody therapies. MDPI 2018-12-17 /pmc/articles/PMC6316644/ /pubmed/30562956 http://dx.doi.org/10.3390/cancers10120519 Text en © 2018 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 | Article Offenhäuser, Carolin Al-Ejeh, Fares Puttick, Simon Ensbey, Kathleen S. Bruce, Zara C. Jamieson, Paul R. Smith, Fiona M. Stringer, Brett W. Carrington, Benjamin Fuchs, Adrian V. Bell, Craig A. Jeffree, Rosalind Rose, Stephen Thurecht, Kristofer J. Boyd, Andrew W. Day, Bryan W. EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma |
title | EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma |
title_full | EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma |
title_fullStr | EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma |
title_full_unstemmed | EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma |
title_short | EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma |
title_sort | epha3 pay-loaded antibody therapeutics for the treatment of glioblastoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316644/ https://www.ncbi.nlm.nih.gov/pubmed/30562956 http://dx.doi.org/10.3390/cancers10120519 |
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