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Linking oncogenesis and immune system evasion in acquired resistance to EGFR-targeting antibodies: Lessons from a preclinical model

Searching for biomarkers that associated with the acquired resistance of malignant cells to epidermal growth factor receptor (EGFR)-targeting monoclonal antibodies is crucial to improve the clinical benefits of these therapeutic agents. We have recently demonstrated that molecular alterations in bot...

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Detalles Bibliográficos
Autores principales: Garrido, Greta, Rabasa, Ailem, Sánchez, Belinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912052/
https://www.ncbi.nlm.nih.gov/pubmed/24498560
http://dx.doi.org/10.4161/onci.26904
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author Garrido, Greta
Rabasa, Ailem
Sánchez, Belinda
author_facet Garrido, Greta
Rabasa, Ailem
Sánchez, Belinda
author_sort Garrido, Greta
collection PubMed
description Searching for biomarkers that associated with the acquired resistance of malignant cells to epidermal growth factor receptor (EGFR)-targeting monoclonal antibodies is crucial to improve the clinical benefits of these therapeutic agents. We have recently demonstrated that molecular alterations in both oncogenic and immunological pathways may be responsible for such an insensitivity. Our findings suggest that a combination of targeted anticancer agents and immunomodulatory drugs may be useful for overcoming the acquired resistance of cancer cells to EGFR-specific monoclonal antibodies.
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spelling pubmed-39120522014-02-04 Linking oncogenesis and immune system evasion in acquired resistance to EGFR-targeting antibodies: Lessons from a preclinical model Garrido, Greta Rabasa, Ailem Sánchez, Belinda Oncoimmunology Author's View Searching for biomarkers that associated with the acquired resistance of malignant cells to epidermal growth factor receptor (EGFR)-targeting monoclonal antibodies is crucial to improve the clinical benefits of these therapeutic agents. We have recently demonstrated that molecular alterations in both oncogenic and immunological pathways may be responsible for such an insensitivity. Our findings suggest that a combination of targeted anticancer agents and immunomodulatory drugs may be useful for overcoming the acquired resistance of cancer cells to EGFR-specific monoclonal antibodies. Landes Bioscience 2013-12-01 2013-11-06 /pmc/articles/PMC3912052/ /pubmed/24498560 http://dx.doi.org/10.4161/onci.26904 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Author's View
Garrido, Greta
Rabasa, Ailem
Sánchez, Belinda
Linking oncogenesis and immune system evasion in acquired resistance to EGFR-targeting antibodies: Lessons from a preclinical model
title Linking oncogenesis and immune system evasion in acquired resistance to EGFR-targeting antibodies: Lessons from a preclinical model
title_full Linking oncogenesis and immune system evasion in acquired resistance to EGFR-targeting antibodies: Lessons from a preclinical model
title_fullStr Linking oncogenesis and immune system evasion in acquired resistance to EGFR-targeting antibodies: Lessons from a preclinical model
title_full_unstemmed Linking oncogenesis and immune system evasion in acquired resistance to EGFR-targeting antibodies: Lessons from a preclinical model
title_short Linking oncogenesis and immune system evasion in acquired resistance to EGFR-targeting antibodies: Lessons from a preclinical model
title_sort linking oncogenesis and immune system evasion in acquired resistance to egfr-targeting antibodies: lessons from a preclinical model
topic Author's View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912052/
https://www.ncbi.nlm.nih.gov/pubmed/24498560
http://dx.doi.org/10.4161/onci.26904
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