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Extracellular matrix as target for antitumor therapy

The aim of the present review is to survey the accumulated knowledge on the extracellular matrix (ECM) of tumors referring to its putative utility as therapeutic target. Following the traditional observation on the extensive morphological alteration in the tumor-affected tissue, the well-documented...

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Detalles Bibliográficos
Autores principales: Harisi, Revekka, Jeney, Andras
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467640/
https://www.ncbi.nlm.nih.gov/pubmed/26089687
http://dx.doi.org/10.2147/OTT.S48883
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author Harisi, Revekka
Jeney, Andras
author_facet Harisi, Revekka
Jeney, Andras
author_sort Harisi, Revekka
collection PubMed
description The aim of the present review is to survey the accumulated knowledge on the extracellular matrix (ECM) of tumors referring to its putative utility as therapeutic target. Following the traditional observation on the extensive morphological alteration in the tumor-affected tissue, the well-documented aberrant cellular regulation indicated that ECM components have an active role in tumor progression. However, due to the diverse functions and variable expression of proteoglycans, matrix proteins, and integrins, it is rather difficult to identify a comprehensive therapeutic target among ECM components. At present, the elevated level of heparanase and the prominent expression of αvβ5 integrin are considered as promising therapeutic targets. The inhibition of glycosaminoglycan offers another promising approach in the treatment of those tumors which are stimulated by proteoglycans. It can be ascertained that a selective ECM inhibitor would be a great asset to control metastasis driven by ECM-mediated signaling.
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spelling pubmed-44676402015-06-18 Extracellular matrix as target for antitumor therapy Harisi, Revekka Jeney, Andras Onco Targets Ther Review The aim of the present review is to survey the accumulated knowledge on the extracellular matrix (ECM) of tumors referring to its putative utility as therapeutic target. Following the traditional observation on the extensive morphological alteration in the tumor-affected tissue, the well-documented aberrant cellular regulation indicated that ECM components have an active role in tumor progression. However, due to the diverse functions and variable expression of proteoglycans, matrix proteins, and integrins, it is rather difficult to identify a comprehensive therapeutic target among ECM components. At present, the elevated level of heparanase and the prominent expression of αvβ5 integrin are considered as promising therapeutic targets. The inhibition of glycosaminoglycan offers another promising approach in the treatment of those tumors which are stimulated by proteoglycans. It can be ascertained that a selective ECM inhibitor would be a great asset to control metastasis driven by ECM-mediated signaling. Dove Medical Press 2015-06-09 /pmc/articles/PMC4467640/ /pubmed/26089687 http://dx.doi.org/10.2147/OTT.S48883 Text en © 2015 Harisi and Jeney. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Harisi, Revekka
Jeney, Andras
Extracellular matrix as target for antitumor therapy
title Extracellular matrix as target for antitumor therapy
title_full Extracellular matrix as target for antitumor therapy
title_fullStr Extracellular matrix as target for antitumor therapy
title_full_unstemmed Extracellular matrix as target for antitumor therapy
title_short Extracellular matrix as target for antitumor therapy
title_sort extracellular matrix as target for antitumor therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467640/
https://www.ncbi.nlm.nih.gov/pubmed/26089687
http://dx.doi.org/10.2147/OTT.S48883
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