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Extracellular Vesicles: New Players in Lymphomas
Lymphomas are heterogeneous diseases, and the term includes a number of histological subtypes that are characterized by different clinical behavior and molecular phenotypes. Valuable information on the presence of lymphoma cell-derived extracellular vesicles (LCEVs) in the bloodstream of patients su...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337615/ https://www.ncbi.nlm.nih.gov/pubmed/30583481 http://dx.doi.org/10.3390/ijms20010041 |
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author | Navarro-Tableros, Victor Gomez, Yonathan Camussi, Giovanni Brizzi, Maria Felice |
author_facet | Navarro-Tableros, Victor Gomez, Yonathan Camussi, Giovanni Brizzi, Maria Felice |
author_sort | Navarro-Tableros, Victor |
collection | PubMed |
description | Lymphomas are heterogeneous diseases, and the term includes a number of histological subtypes that are characterized by different clinical behavior and molecular phenotypes. Valuable information on the presence of lymphoma cell-derived extracellular vesicles (LCEVs) in the bloodstream of patients suffering from this hematological cancer has recently been provided. In particular, it has been reported that the number and phenotype of LCEVs can both change as the disease progresses, as well as after treatment. Moreover, the role that LCEVs play in driving tumor immune escape has been reported. This makes LCEVs potential novel clinical tools for diagnosis, disease progression, and chemoresistance. LCEVs express surface markers and convey specific molecules in accordance with their cell of origin, which can be used as targets and thus lead to the development of specific therapeutics. This may be particularly relevant since circulating LCEVs are known to save lymphoma cells from anti-cluster of differentiation (CD)20-induced complement-dependent cytotoxicity. Therefore, effort should be directed toward investigating the feasibility of using LCEVs as predictive biomarkers of disease progression and/or response to treatment that can be translated to clinical use. The use of liquid biopsies in combination with serum EV quantification and cargo analysis have been also considered as potential approaches that can be pursued in the future. Upcoming research will also focus on the identification of specific molecular targets in order to generate vaccines and/or antibodies against LCEVs. Finally, the removal of circulating LCEVs has been proposed as a simple and non-invasive treatment approach. We herein provide an overview of the role of LCEVs in lymphoma diagnosis, immune tolerance, and drug resistance. In addition, alternative protocols that utilize LCEVs as therapeutic targets are discussed. |
format | Online Article Text |
id | pubmed-6337615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63376152019-01-22 Extracellular Vesicles: New Players in Lymphomas Navarro-Tableros, Victor Gomez, Yonathan Camussi, Giovanni Brizzi, Maria Felice Int J Mol Sci Review Lymphomas are heterogeneous diseases, and the term includes a number of histological subtypes that are characterized by different clinical behavior and molecular phenotypes. Valuable information on the presence of lymphoma cell-derived extracellular vesicles (LCEVs) in the bloodstream of patients suffering from this hematological cancer has recently been provided. In particular, it has been reported that the number and phenotype of LCEVs can both change as the disease progresses, as well as after treatment. Moreover, the role that LCEVs play in driving tumor immune escape has been reported. This makes LCEVs potential novel clinical tools for diagnosis, disease progression, and chemoresistance. LCEVs express surface markers and convey specific molecules in accordance with their cell of origin, which can be used as targets and thus lead to the development of specific therapeutics. This may be particularly relevant since circulating LCEVs are known to save lymphoma cells from anti-cluster of differentiation (CD)20-induced complement-dependent cytotoxicity. Therefore, effort should be directed toward investigating the feasibility of using LCEVs as predictive biomarkers of disease progression and/or response to treatment that can be translated to clinical use. The use of liquid biopsies in combination with serum EV quantification and cargo analysis have been also considered as potential approaches that can be pursued in the future. Upcoming research will also focus on the identification of specific molecular targets in order to generate vaccines and/or antibodies against LCEVs. Finally, the removal of circulating LCEVs has been proposed as a simple and non-invasive treatment approach. We herein provide an overview of the role of LCEVs in lymphoma diagnosis, immune tolerance, and drug resistance. In addition, alternative protocols that utilize LCEVs as therapeutic targets are discussed. MDPI 2018-12-21 /pmc/articles/PMC6337615/ /pubmed/30583481 http://dx.doi.org/10.3390/ijms20010041 Text en © 2018 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 Navarro-Tableros, Victor Gomez, Yonathan Camussi, Giovanni Brizzi, Maria Felice Extracellular Vesicles: New Players in Lymphomas |
title | Extracellular Vesicles: New Players in Lymphomas |
title_full | Extracellular Vesicles: New Players in Lymphomas |
title_fullStr | Extracellular Vesicles: New Players in Lymphomas |
title_full_unstemmed | Extracellular Vesicles: New Players in Lymphomas |
title_short | Extracellular Vesicles: New Players in Lymphomas |
title_sort | extracellular vesicles: new players in lymphomas |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337615/ https://www.ncbi.nlm.nih.gov/pubmed/30583481 http://dx.doi.org/10.3390/ijms20010041 |
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