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Extracellular Vesicles – Biomarkers and Effectors of the Cellular Interactome in Cancer

In multicellular organisms both health and disease are defined by patterns of communication between the constituent cells. In addition to networks of soluble mediators, cells are also programed to exchange complex messages pre-assembled as multimolecular cargo of membraneous structures known extrace...

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Autor principal: Rak, Janusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589665/
https://www.ncbi.nlm.nih.gov/pubmed/23508692
http://dx.doi.org/10.3389/fphar.2013.00021
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author Rak, Janusz
author_facet Rak, Janusz
author_sort Rak, Janusz
collection PubMed
description In multicellular organisms both health and disease are defined by patterns of communication between the constituent cells. In addition to networks of soluble mediators, cells are also programed to exchange complex messages pre-assembled as multimolecular cargo of membraneous structures known extracellular vesicles (EV). Several biogenetic pathways produce EVs with different properties, and known as exosomes, ectosomes, and apoptotic bodies. In cancer, EVs carry molecular signatures and effectors of the disease, such as mutant oncoproteins, oncogenic transcripts, microRNA, and DNA sequences. Intercellular trafficking of such EVs (oncosomes) may contribute to horizontal cellular transformation, phenotypic reprograming, and functional re-education of recipient cells, both locally and systemically. The EV-mediated, reciprocal molecular exchange also includes tumor suppressors, phosphoproteins, proteases, growth factors, and bioactive lipids, all of which participate in the functional integration of multiple cells and their collective involvement in tumor angiogenesis, inflammation, immunity, coagulopathy, mobilization of bone marrow-derived effectors, metastasis, drug resistance, or cellular stemness. In cases where the EV role is rate limiting their production and uptake may represent and unexplored anticancer therapy target. Moreover, oncosomes circulating in biofluids of cancer patients offer an unprecedented, remote, and non-invasive access to crucial molecular information about cancer cells, including their driver mutations, classifiers, molecular subtypes, therapeutic targets, and biomarkers of drug resistance. New nanotechnologies are being developed to exploit this unique biomarker platform. Indeed, embracing the notion that human cancers are defined not only by processes occurring within cancer cells, but also between them, and amidst the altered tumor and systemic microenvironment may open new diagnostic and therapeutic opportunities.
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spelling pubmed-35896652013-03-18 Extracellular Vesicles – Biomarkers and Effectors of the Cellular Interactome in Cancer Rak, Janusz Front Pharmacol Pharmacology In multicellular organisms both health and disease are defined by patterns of communication between the constituent cells. In addition to networks of soluble mediators, cells are also programed to exchange complex messages pre-assembled as multimolecular cargo of membraneous structures known extracellular vesicles (EV). Several biogenetic pathways produce EVs with different properties, and known as exosomes, ectosomes, and apoptotic bodies. In cancer, EVs carry molecular signatures and effectors of the disease, such as mutant oncoproteins, oncogenic transcripts, microRNA, and DNA sequences. Intercellular trafficking of such EVs (oncosomes) may contribute to horizontal cellular transformation, phenotypic reprograming, and functional re-education of recipient cells, both locally and systemically. The EV-mediated, reciprocal molecular exchange also includes tumor suppressors, phosphoproteins, proteases, growth factors, and bioactive lipids, all of which participate in the functional integration of multiple cells and their collective involvement in tumor angiogenesis, inflammation, immunity, coagulopathy, mobilization of bone marrow-derived effectors, metastasis, drug resistance, or cellular stemness. In cases where the EV role is rate limiting their production and uptake may represent and unexplored anticancer therapy target. Moreover, oncosomes circulating in biofluids of cancer patients offer an unprecedented, remote, and non-invasive access to crucial molecular information about cancer cells, including their driver mutations, classifiers, molecular subtypes, therapeutic targets, and biomarkers of drug resistance. New nanotechnologies are being developed to exploit this unique biomarker platform. Indeed, embracing the notion that human cancers are defined not only by processes occurring within cancer cells, but also between them, and amidst the altered tumor and systemic microenvironment may open new diagnostic and therapeutic opportunities. Frontiers Media S.A. 2013-03-06 /pmc/articles/PMC3589665/ /pubmed/23508692 http://dx.doi.org/10.3389/fphar.2013.00021 Text en Copyright © 2013 Rak. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Pharmacology
Rak, Janusz
Extracellular Vesicles – Biomarkers and Effectors of the Cellular Interactome in Cancer
title Extracellular Vesicles – Biomarkers and Effectors of the Cellular Interactome in Cancer
title_full Extracellular Vesicles – Biomarkers and Effectors of the Cellular Interactome in Cancer
title_fullStr Extracellular Vesicles – Biomarkers and Effectors of the Cellular Interactome in Cancer
title_full_unstemmed Extracellular Vesicles – Biomarkers and Effectors of the Cellular Interactome in Cancer
title_short Extracellular Vesicles – Biomarkers and Effectors of the Cellular Interactome in Cancer
title_sort extracellular vesicles – biomarkers and effectors of the cellular interactome in cancer
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589665/
https://www.ncbi.nlm.nih.gov/pubmed/23508692
http://dx.doi.org/10.3389/fphar.2013.00021
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