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The complexity of integrins in cancer and new scopes for therapeutic targeting

Cancer is a complex disease and progresses within a dynamically evolving extracellular matrix that controls virtually every aspect of the tumour and tumour-associated cells. Interactions with the extracellular microenvironment are predominately mediated by a family of cell-surface transmembrane rece...

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Autores principales: Hamidi, Hellyeh, Pietilä, Mika, Ivaska, Johanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117799/
https://www.ncbi.nlm.nih.gov/pubmed/27685444
http://dx.doi.org/10.1038/bjc.2016.312
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author Hamidi, Hellyeh
Pietilä, Mika
Ivaska, Johanna
author_facet Hamidi, Hellyeh
Pietilä, Mika
Ivaska, Johanna
author_sort Hamidi, Hellyeh
collection PubMed
description Cancer is a complex disease and progresses within a dynamically evolving extracellular matrix that controls virtually every aspect of the tumour and tumour-associated cells. Interactions with the extracellular microenvironment are predominately mediated by a family of cell-surface transmembrane receptors called integrins. Integrin–matrix engagement leads to the formation of adhesion plaques, consisting of signalling and adaptor proteins, at the plasma membrane that link the extracellular matrix to the regulation of the cell cytoskeleton. In this review, we will highlight exciting data that identify new roles for integrins and integrin-dependent signalling in cancer away from the plasma membrane, discuss the implications of integrin-dependent regulation of Met and ErbB2 growth factor receptors and highlight the role of specific integrins in different stages of cancer development including maintenance of cancer stem cells.
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spelling pubmed-51177992016-12-16 The complexity of integrins in cancer and new scopes for therapeutic targeting Hamidi, Hellyeh Pietilä, Mika Ivaska, Johanna Br J Cancer Minireview Cancer is a complex disease and progresses within a dynamically evolving extracellular matrix that controls virtually every aspect of the tumour and tumour-associated cells. Interactions with the extracellular microenvironment are predominately mediated by a family of cell-surface transmembrane receptors called integrins. Integrin–matrix engagement leads to the formation of adhesion plaques, consisting of signalling and adaptor proteins, at the plasma membrane that link the extracellular matrix to the regulation of the cell cytoskeleton. In this review, we will highlight exciting data that identify new roles for integrins and integrin-dependent signalling in cancer away from the plasma membrane, discuss the implications of integrin-dependent regulation of Met and ErbB2 growth factor receptors and highlight the role of specific integrins in different stages of cancer development including maintenance of cancer stem cells. Nature Publishing Group 2016-10-25 2016-09-29 /pmc/articles/PMC5117799/ /pubmed/27685444 http://dx.doi.org/10.1038/bjc.2016.312 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Minireview
Hamidi, Hellyeh
Pietilä, Mika
Ivaska, Johanna
The complexity of integrins in cancer and new scopes for therapeutic targeting
title The complexity of integrins in cancer and new scopes for therapeutic targeting
title_full The complexity of integrins in cancer and new scopes for therapeutic targeting
title_fullStr The complexity of integrins in cancer and new scopes for therapeutic targeting
title_full_unstemmed The complexity of integrins in cancer and new scopes for therapeutic targeting
title_short The complexity of integrins in cancer and new scopes for therapeutic targeting
title_sort complexity of integrins in cancer and new scopes for therapeutic targeting
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117799/
https://www.ncbi.nlm.nih.gov/pubmed/27685444
http://dx.doi.org/10.1038/bjc.2016.312
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