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Integrins as Therapeutic Targets: Successes and Cancers

Integrins are transmembrane receptors that are central to the biology of many human pathologies. Classically mediating cell-extracellular matrix and cell-cell interaction, and with an emerging role as local activators of TGFβ, they influence cancer, fibrosis, thrombosis and inflammation. Their ligan...

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Detalles Bibliográficos
Autores principales: Raab-Westphal, Sabine, Marshall, John F., Goodman, Simon L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615325/
https://www.ncbi.nlm.nih.gov/pubmed/28832494
http://dx.doi.org/10.3390/cancers9090110
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author Raab-Westphal, Sabine
Marshall, John F.
Goodman, Simon L.
author_facet Raab-Westphal, Sabine
Marshall, John F.
Goodman, Simon L.
author_sort Raab-Westphal, Sabine
collection PubMed
description Integrins are transmembrane receptors that are central to the biology of many human pathologies. Classically mediating cell-extracellular matrix and cell-cell interaction, and with an emerging role as local activators of TGFβ, they influence cancer, fibrosis, thrombosis and inflammation. Their ligand binding and some regulatory sites are extracellular and sensitive to pharmacological intervention, as proven by the clinical success of seven drugs targeting them. The six drugs on the market in 2016 generated revenues of some US$3.5 billion, mainly from inhibitors of α4-series integrins. In this review we examine the current developments in integrin therapeutics, especially in cancer, and comment on the health economic implications of these developments.
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spelling pubmed-56153252017-09-28 Integrins as Therapeutic Targets: Successes and Cancers Raab-Westphal, Sabine Marshall, John F. Goodman, Simon L. Cancers (Basel) Review Integrins are transmembrane receptors that are central to the biology of many human pathologies. Classically mediating cell-extracellular matrix and cell-cell interaction, and with an emerging role as local activators of TGFβ, they influence cancer, fibrosis, thrombosis and inflammation. Their ligand binding and some regulatory sites are extracellular and sensitive to pharmacological intervention, as proven by the clinical success of seven drugs targeting them. The six drugs on the market in 2016 generated revenues of some US$3.5 billion, mainly from inhibitors of α4-series integrins. In this review we examine the current developments in integrin therapeutics, especially in cancer, and comment on the health economic implications of these developments. MDPI 2017-08-23 /pmc/articles/PMC5615325/ /pubmed/28832494 http://dx.doi.org/10.3390/cancers9090110 Text en © 2017 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 Review
Raab-Westphal, Sabine
Marshall, John F.
Goodman, Simon L.
Integrins as Therapeutic Targets: Successes and Cancers
title Integrins as Therapeutic Targets: Successes and Cancers
title_full Integrins as Therapeutic Targets: Successes and Cancers
title_fullStr Integrins as Therapeutic Targets: Successes and Cancers
title_full_unstemmed Integrins as Therapeutic Targets: Successes and Cancers
title_short Integrins as Therapeutic Targets: Successes and Cancers
title_sort integrins as therapeutic targets: successes and cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615325/
https://www.ncbi.nlm.nih.gov/pubmed/28832494
http://dx.doi.org/10.3390/cancers9090110
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