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Use of multitarget tyrosine kinase inhibitors to attenuate platelet-derived growth factor signalling in lung disease

Platelet-derived growth factors (PDGFs) and their receptors (PDGFRs) play a fundamental role in the embryonic development of the lung. Aberrant PDGF signalling has been documented convincingly in a large variety of pulmonary diseases, including idiopathic pulmonary arterial hypertension, lung cancer...

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Detalles Bibliográficos
Autores principales: Kanaan, Rana, Strange, Charlie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488848/
https://www.ncbi.nlm.nih.gov/pubmed/29070579
http://dx.doi.org/10.1183/16000617.0061-2017
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author Kanaan, Rana
Strange, Charlie
author_facet Kanaan, Rana
Strange, Charlie
author_sort Kanaan, Rana
collection PubMed
description Platelet-derived growth factors (PDGFs) and their receptors (PDGFRs) play a fundamental role in the embryonic development of the lung. Aberrant PDGF signalling has been documented convincingly in a large variety of pulmonary diseases, including idiopathic pulmonary arterial hypertension, lung cancer and lung fibrosis. Targeting PDGF signalling has been proven to be effective in these diseases. In clinical practice, the most effective way to block PDGF signalling is to inhibit the activity of the intracellular PDGFR kinases. Although the mechanism of action of such drugs is not specific for PDGF signalling, the medications have a broad therapeutic index that allows clinical use. The safety profile and therapeutic opportunities of these and future medications that target PDGFs and PDGFRs are reviewed.
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spelling pubmed-94888482022-11-14 Use of multitarget tyrosine kinase inhibitors to attenuate platelet-derived growth factor signalling in lung disease Kanaan, Rana Strange, Charlie Eur Respir Rev Reviews Platelet-derived growth factors (PDGFs) and their receptors (PDGFRs) play a fundamental role in the embryonic development of the lung. Aberrant PDGF signalling has been documented convincingly in a large variety of pulmonary diseases, including idiopathic pulmonary arterial hypertension, lung cancer and lung fibrosis. Targeting PDGF signalling has been proven to be effective in these diseases. In clinical practice, the most effective way to block PDGF signalling is to inhibit the activity of the intracellular PDGFR kinases. Although the mechanism of action of such drugs is not specific for PDGF signalling, the medications have a broad therapeutic index that allows clinical use. The safety profile and therapeutic opportunities of these and future medications that target PDGFs and PDGFRs are reviewed. European Respiratory Society 2017-10-25 /pmc/articles/PMC9488848/ /pubmed/29070579 http://dx.doi.org/10.1183/16000617.0061-2017 Text en Copyright ©ERS 2017. https://creativecommons.org/licenses/by-nc/4.0/ERR articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
spellingShingle Reviews
Kanaan, Rana
Strange, Charlie
Use of multitarget tyrosine kinase inhibitors to attenuate platelet-derived growth factor signalling in lung disease
title Use of multitarget tyrosine kinase inhibitors to attenuate platelet-derived growth factor signalling in lung disease
title_full Use of multitarget tyrosine kinase inhibitors to attenuate platelet-derived growth factor signalling in lung disease
title_fullStr Use of multitarget tyrosine kinase inhibitors to attenuate platelet-derived growth factor signalling in lung disease
title_full_unstemmed Use of multitarget tyrosine kinase inhibitors to attenuate platelet-derived growth factor signalling in lung disease
title_short Use of multitarget tyrosine kinase inhibitors to attenuate platelet-derived growth factor signalling in lung disease
title_sort use of multitarget tyrosine kinase inhibitors to attenuate platelet-derived growth factor signalling in lung disease
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488848/
https://www.ncbi.nlm.nih.gov/pubmed/29070579
http://dx.doi.org/10.1183/16000617.0061-2017
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