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42. IDENTIFICATION OF BRAIN METASTASIS VULNERABILITIES USING METPLATFORM

The diagnosis of brain metastasis involves high morbidity and mortality and remains an unmet clinical need in spite of being the most common tumor in the brain. Exclusion of these cancer patients from clinical trials is a major cause of their limited therapeutic options. In this study, we report a n...

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Autores principales: Zhu, Lucía, Yebra, Natalia, Retana, Diana, Blanco-Aparicio, Carmen, Martínez, Sonia, Soffietti, Riccardo, Bertero, Luca, Cassoni, Paola, Weiss, Tobias, Muñoz, Javier, Manuel Sepúlveda, Juan, Pérez-Núñez, Ángel, Hernández-Laín, Aurelio, Toldos, Óscar, Caleiras, Eduardo, Nör, Carolina, Taylor, Michael D, Weller, Michael, Pastor, Joaquín, Valiente, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401369/
http://dx.doi.org/10.1093/noajnl/vdaa073.030
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author Zhu, Lucía
Yebra, Natalia
Retana, Diana
Blanco-Aparicio, Carmen
Martínez, Sonia
Soffietti, Riccardo
Bertero, Luca
Cassoni, Paola
Weiss, Tobias
Muñoz, Javier
Manuel Sepúlveda, Juan
Pérez-Núñez, Ángel
Hernández-Laín, Aurelio
Toldos, Óscar
Caleiras, Eduardo
Nör, Carolina
Taylor, Michael D
Weller, Michael
Pastor, Joaquín
Valiente, Manuel
author_facet Zhu, Lucía
Yebra, Natalia
Retana, Diana
Blanco-Aparicio, Carmen
Martínez, Sonia
Soffietti, Riccardo
Bertero, Luca
Cassoni, Paola
Weiss, Tobias
Muñoz, Javier
Manuel Sepúlveda, Juan
Pérez-Núñez, Ángel
Hernández-Laín, Aurelio
Toldos, Óscar
Caleiras, Eduardo
Nör, Carolina
Taylor, Michael D
Weller, Michael
Pastor, Joaquín
Valiente, Manuel
author_sort Zhu, Lucía
collection PubMed
description The diagnosis of brain metastasis involves high morbidity and mortality and remains an unmet clinical need in spite of being the most common tumor in the brain. Exclusion of these cancer patients from clinical trials is a major cause of their limited therapeutic options. In this study, we report a novel drug-screening platform (METPlatform) based on organotypic cultures which allows identifying effective anti-metastasis agents in the presence of the organ microenvironment. We have applied this approach to clinically relevant stages of brain metastasis using both experimental models and human tumor tissue (by performing patient-derived organotypic cultures). We identified heat shock protein 90 (HSP90) as a promising therapeutic target for brain metastasis. Debio-0932, a blood-brain barrier permeable HSP90 inhibitor, shows high potency against mouse and human brain metastases from melanoma, lung and breast adenocarcinoma with distinct oncogenomic profiles at clinically relevant stages of the disease, including a novel model of local relapse after neurosurgery. Furthermore, we have also used METPlatform to perform unbiased proteomics of brain metastases in situ. By applying this analysis to brain metastases treated with the chaperone inhibitor, we uncovered non-canonical clients of HSP90 as potential novel mediators of brain metastasis and actionable mechanisms of resistance driven by autophagy. Combined therapy using HSP90 and autophagy inhibitors showed synergistic effects compared to sublethal concentrations of each monotherapy, demonstrating the potential of METPlatform to design and test rationale combination therapies to target metastasis more effectively. In conclusion, our work validates METPlatform as a potent resource for metastasis research integrating drug-screening and unbiased omic approaches that is fully compatible with human samples and questions the rationale of excluding patients with brain metastasis from clinical trials. We envision that METPlatform will be established as a clinically relevant strategy to personalize the management of metastatic disease in the brain and elsewhere.
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spelling pubmed-74013692020-08-06 42. IDENTIFICATION OF BRAIN METASTASIS VULNERABILITIES USING METPLATFORM Zhu, Lucía Yebra, Natalia Retana, Diana Blanco-Aparicio, Carmen Martínez, Sonia Soffietti, Riccardo Bertero, Luca Cassoni, Paola Weiss, Tobias Muñoz, Javier Manuel Sepúlveda, Juan Pérez-Núñez, Ángel Hernández-Laín, Aurelio Toldos, Óscar Caleiras, Eduardo Nör, Carolina Taylor, Michael D Weller, Michael Pastor, Joaquín Valiente, Manuel Neurooncol Adv Supplement Abstracts The diagnosis of brain metastasis involves high morbidity and mortality and remains an unmet clinical need in spite of being the most common tumor in the brain. Exclusion of these cancer patients from clinical trials is a major cause of their limited therapeutic options. In this study, we report a novel drug-screening platform (METPlatform) based on organotypic cultures which allows identifying effective anti-metastasis agents in the presence of the organ microenvironment. We have applied this approach to clinically relevant stages of brain metastasis using both experimental models and human tumor tissue (by performing patient-derived organotypic cultures). We identified heat shock protein 90 (HSP90) as a promising therapeutic target for brain metastasis. Debio-0932, a blood-brain barrier permeable HSP90 inhibitor, shows high potency against mouse and human brain metastases from melanoma, lung and breast adenocarcinoma with distinct oncogenomic profiles at clinically relevant stages of the disease, including a novel model of local relapse after neurosurgery. Furthermore, we have also used METPlatform to perform unbiased proteomics of brain metastases in situ. By applying this analysis to brain metastases treated with the chaperone inhibitor, we uncovered non-canonical clients of HSP90 as potential novel mediators of brain metastasis and actionable mechanisms of resistance driven by autophagy. Combined therapy using HSP90 and autophagy inhibitors showed synergistic effects compared to sublethal concentrations of each monotherapy, demonstrating the potential of METPlatform to design and test rationale combination therapies to target metastasis more effectively. In conclusion, our work validates METPlatform as a potent resource for metastasis research integrating drug-screening and unbiased omic approaches that is fully compatible with human samples and questions the rationale of excluding patients with brain metastasis from clinical trials. We envision that METPlatform will be established as a clinically relevant strategy to personalize the management of metastatic disease in the brain and elsewhere. Oxford University Press 2020-08-04 /pmc/articles/PMC7401369/ http://dx.doi.org/10.1093/noajnl/vdaa073.030 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Supplement Abstracts
Zhu, Lucía
Yebra, Natalia
Retana, Diana
Blanco-Aparicio, Carmen
Martínez, Sonia
Soffietti, Riccardo
Bertero, Luca
Cassoni, Paola
Weiss, Tobias
Muñoz, Javier
Manuel Sepúlveda, Juan
Pérez-Núñez, Ángel
Hernández-Laín, Aurelio
Toldos, Óscar
Caleiras, Eduardo
Nör, Carolina
Taylor, Michael D
Weller, Michael
Pastor, Joaquín
Valiente, Manuel
42. IDENTIFICATION OF BRAIN METASTASIS VULNERABILITIES USING METPLATFORM
title 42. IDENTIFICATION OF BRAIN METASTASIS VULNERABILITIES USING METPLATFORM
title_full 42. IDENTIFICATION OF BRAIN METASTASIS VULNERABILITIES USING METPLATFORM
title_fullStr 42. IDENTIFICATION OF BRAIN METASTASIS VULNERABILITIES USING METPLATFORM
title_full_unstemmed 42. IDENTIFICATION OF BRAIN METASTASIS VULNERABILITIES USING METPLATFORM
title_short 42. IDENTIFICATION OF BRAIN METASTASIS VULNERABILITIES USING METPLATFORM
title_sort 42. identification of brain metastasis vulnerabilities using metplatform
topic Supplement Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401369/
http://dx.doi.org/10.1093/noajnl/vdaa073.030
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