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Exosome-Based Cell-Cell Communication in the Tumor Microenvironment

Tumors are not isolated entities, but complex systemic networks involving cell-cell communication between transformed and non-transformed cells. The milieu created by tumor-associated cells may either support or halt tumor progression. In addition to cell-cell contact, cells communicate through secr...

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Autores principales: Maia, Joana, Caja, Sergio, Strano Moraes, Maria Carolina, Couto, Nuno, Costa-Silva, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826063/
https://www.ncbi.nlm.nih.gov/pubmed/29515996
http://dx.doi.org/10.3389/fcell.2018.00018
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author Maia, Joana
Caja, Sergio
Strano Moraes, Maria Carolina
Couto, Nuno
Costa-Silva, Bruno
author_facet Maia, Joana
Caja, Sergio
Strano Moraes, Maria Carolina
Couto, Nuno
Costa-Silva, Bruno
author_sort Maia, Joana
collection PubMed
description Tumors are not isolated entities, but complex systemic networks involving cell-cell communication between transformed and non-transformed cells. The milieu created by tumor-associated cells may either support or halt tumor progression. In addition to cell-cell contact, cells communicate through secreted factors via a highly complex system involving characteristics such as ligand concentration, receptor expression and integration of diverse signaling pathways. Of these, extracellular vesicles, such as exosomes, are emerging as novel cell-cell communication mediators in physiological and pathological scenarios. Exosomes, membrane vesicles of endocytic origin released by all cells (both healthy and diseased), ranging in size from 30 to 150 nm, transport all the main biomolecules, including lipids, proteins, DNAs, messenger RNAs and microRNA, and perform intercellular transfer of components, locally and systemically. By acting not only in tumor cells, but also in tumor-associated cells such as fibroblasts, endothelium, leukocytes and progenitor cells, tumor- and non-tumor cells-derived exosomes have emerged as new players in tumor growth and invasion, tumor-associated angiogenesis, tissue inflammation and immunologic remodeling. In addition, due to their property of carrying molecules from their cell of origin to the peripheral circulation, exosomes have been increasingly studied as sources of tumor biomarkers in liquid biopsies. Here we review the current literature on the participation of exosomes in the communication between tumor and tumor-associated cells, highlighting the role of this process in the setup of tumor microenvironments that modulate tumor initiation and metastasis.
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spelling pubmed-58260632018-03-07 Exosome-Based Cell-Cell Communication in the Tumor Microenvironment Maia, Joana Caja, Sergio Strano Moraes, Maria Carolina Couto, Nuno Costa-Silva, Bruno Front Cell Dev Biol Cell and Developmental Biology Tumors are not isolated entities, but complex systemic networks involving cell-cell communication between transformed and non-transformed cells. The milieu created by tumor-associated cells may either support or halt tumor progression. In addition to cell-cell contact, cells communicate through secreted factors via a highly complex system involving characteristics such as ligand concentration, receptor expression and integration of diverse signaling pathways. Of these, extracellular vesicles, such as exosomes, are emerging as novel cell-cell communication mediators in physiological and pathological scenarios. Exosomes, membrane vesicles of endocytic origin released by all cells (both healthy and diseased), ranging in size from 30 to 150 nm, transport all the main biomolecules, including lipids, proteins, DNAs, messenger RNAs and microRNA, and perform intercellular transfer of components, locally and systemically. By acting not only in tumor cells, but also in tumor-associated cells such as fibroblasts, endothelium, leukocytes and progenitor cells, tumor- and non-tumor cells-derived exosomes have emerged as new players in tumor growth and invasion, tumor-associated angiogenesis, tissue inflammation and immunologic remodeling. In addition, due to their property of carrying molecules from their cell of origin to the peripheral circulation, exosomes have been increasingly studied as sources of tumor biomarkers in liquid biopsies. Here we review the current literature on the participation of exosomes in the communication between tumor and tumor-associated cells, highlighting the role of this process in the setup of tumor microenvironments that modulate tumor initiation and metastasis. Frontiers Media S.A. 2018-02-20 /pmc/articles/PMC5826063/ /pubmed/29515996 http://dx.doi.org/10.3389/fcell.2018.00018 Text en Copyright © 2018 Maia, Caja, Strano Moraes, Couto and Costa-Silva. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Maia, Joana
Caja, Sergio
Strano Moraes, Maria Carolina
Couto, Nuno
Costa-Silva, Bruno
Exosome-Based Cell-Cell Communication in the Tumor Microenvironment
title Exosome-Based Cell-Cell Communication in the Tumor Microenvironment
title_full Exosome-Based Cell-Cell Communication in the Tumor Microenvironment
title_fullStr Exosome-Based Cell-Cell Communication in the Tumor Microenvironment
title_full_unstemmed Exosome-Based Cell-Cell Communication in the Tumor Microenvironment
title_short Exosome-Based Cell-Cell Communication in the Tumor Microenvironment
title_sort exosome-based cell-cell communication in the tumor microenvironment
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826063/
https://www.ncbi.nlm.nih.gov/pubmed/29515996
http://dx.doi.org/10.3389/fcell.2018.00018
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