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Emerging targets for cancer treatment: S100A9/RAGE

Developing better treatments that work for the majority of patients with brain metastasis (BM) is highly necessary. Complementarily, avoiding those therapeutic procedures that will not benefit a specific patient is also very relevant. In general, existing therapies for patients with BM could be impr...

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Detalles Bibliográficos
Autores principales: Valiente, M., Sepúlveda, J.M., Pérez, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860424/
https://www.ncbi.nlm.nih.gov/pubmed/36652782
http://dx.doi.org/10.1016/j.esmoop.2022.100751
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author Valiente, M.
Sepúlveda, J.M.
Pérez, A.
author_facet Valiente, M.
Sepúlveda, J.M.
Pérez, A.
author_sort Valiente, M.
collection PubMed
description Developing better treatments that work for the majority of patients with brain metastasis (BM) is highly necessary. Complementarily, avoiding those therapeutic procedures that will not benefit a specific patient is also very relevant. In general, existing therapies for patients with BM could be improved in terms of molecular stratification and therapeutic efficacy. By questioning the benefit of whole brain radiotherapy as provided nowadays and the lack of biomarkers detecting radioresistance, we identified S100A9 and receptor for advanced glycation end-products (RAGE) as a liquid biopsy biomarker and a potential target for a radiosensitizer, respectively. Both of them are being clinically tested as part of the first comprehensive molecular strategy to personalized radiotherapy in BM.
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spelling pubmed-98604242023-01-22 Emerging targets for cancer treatment: S100A9/RAGE Valiente, M. Sepúlveda, J.M. Pérez, A. ESMO Open Review Developing better treatments that work for the majority of patients with brain metastasis (BM) is highly necessary. Complementarily, avoiding those therapeutic procedures that will not benefit a specific patient is also very relevant. In general, existing therapies for patients with BM could be improved in terms of molecular stratification and therapeutic efficacy. By questioning the benefit of whole brain radiotherapy as provided nowadays and the lack of biomarkers detecting radioresistance, we identified S100A9 and receptor for advanced glycation end-products (RAGE) as a liquid biopsy biomarker and a potential target for a radiosensitizer, respectively. Both of them are being clinically tested as part of the first comprehensive molecular strategy to personalized radiotherapy in BM. Elsevier 2023-01-16 /pmc/articles/PMC9860424/ /pubmed/36652782 http://dx.doi.org/10.1016/j.esmoop.2022.100751 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Valiente, M.
Sepúlveda, J.M.
Pérez, A.
Emerging targets for cancer treatment: S100A9/RAGE
title Emerging targets for cancer treatment: S100A9/RAGE
title_full Emerging targets for cancer treatment: S100A9/RAGE
title_fullStr Emerging targets for cancer treatment: S100A9/RAGE
title_full_unstemmed Emerging targets for cancer treatment: S100A9/RAGE
title_short Emerging targets for cancer treatment: S100A9/RAGE
title_sort emerging targets for cancer treatment: s100a9/rage
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860424/
https://www.ncbi.nlm.nih.gov/pubmed/36652782
http://dx.doi.org/10.1016/j.esmoop.2022.100751
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