3D Cell Cultures as Prospective Models to Study Extracellular Vesicles in Cancer

The improvement of culturing techniques to model the environment and physiological conditions surrounding tumors has also been applied to the study of extracellular vesicles (EVs) in cancer research. EVs role is not only limited to cell-to-cell communication in tumor physiology, they are also a prom...

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Main Authors: Guillermo Bordanaba-Florit, Iratxe Madarieta, Beatriz Olalde, Juan M. Falcón-Pérez, Félix Royo
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/2/307
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author Guillermo Bordanaba-Florit
Iratxe Madarieta
Beatriz Olalde
Juan M. Falcón-Pérez
Félix Royo
author_facet Guillermo Bordanaba-Florit
Iratxe Madarieta
Beatriz Olalde
Juan M. Falcón-Pérez
Félix Royo
author_sort Guillermo Bordanaba-Florit
collection DOAJ
description The improvement of culturing techniques to model the environment and physiological conditions surrounding tumors has also been applied to the study of extracellular vesicles (EVs) in cancer research. EVs role is not only limited to cell-to-cell communication in tumor physiology, they are also a promising source of biomarkers, and a tool to deliver drugs and induce antitumoral activity. In the present review, we have addressed the improvements achieved by using 3D culture models to evaluate the role of EVs in tumor progression and the potential applications of EVs in diagnostics and therapeutics. The most employed assays are gel-based spheroids, often utilized to examine the cell invasion rate and angiogenesis markers upon EVs treatment. To study EVs as drug carriers, a more complex multicellular cultures and organoids from cancer stem cell populations have been developed. Such strategies provide a closer response to in vivo physiology observed responses. They are also the best models to understand the complex interactions between different populations of cells and the extracellular matrix, in which tumor-derived EVs modify epithelial or mesenchymal cells to become protumor agents. Finally, the growth of cells in 3D bioreactor-like systems is appointed as the best approach to industrial EVs production, a necessary step toward clinical translation of EVs-based therapy.
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spelling doaj.art-78725dd73b6a4f688dbe54e2b7c9408e2023-12-03T13:23:24ZengMDPI AGCancers2072-66942021-01-0113230710.3390/cancers130203073D Cell Cultures as Prospective Models to Study Extracellular Vesicles in CancerGuillermo Bordanaba-Florit0Iratxe Madarieta1Beatriz Olalde2Juan M. Falcón-Pérez3Félix Royo4Center for Cooperative Research in Biosciences (CIC bioGUNE), Exosomes Laboratory, Basque Research and Technology Alliance (BRTA), E48160 Derio, SpainTECNALIA Basque Research and Technology Alliance (BRTA), E20009 Donostia San Sebastian, SpainTECNALIA Basque Research and Technology Alliance (BRTA), E20009 Donostia San Sebastian, SpainCenter for Cooperative Research in Biosciences (CIC bioGUNE), Exosomes Laboratory, Basque Research and Technology Alliance (BRTA), E48160 Derio, SpainCenter for Cooperative Research in Biosciences (CIC bioGUNE), Exosomes Laboratory, Basque Research and Technology Alliance (BRTA), E48160 Derio, SpainThe improvement of culturing techniques to model the environment and physiological conditions surrounding tumors has also been applied to the study of extracellular vesicles (EVs) in cancer research. EVs role is not only limited to cell-to-cell communication in tumor physiology, they are also a promising source of biomarkers, and a tool to deliver drugs and induce antitumoral activity. In the present review, we have addressed the improvements achieved by using 3D culture models to evaluate the role of EVs in tumor progression and the potential applications of EVs in diagnostics and therapeutics. The most employed assays are gel-based spheroids, often utilized to examine the cell invasion rate and angiogenesis markers upon EVs treatment. To study EVs as drug carriers, a more complex multicellular cultures and organoids from cancer stem cell populations have been developed. Such strategies provide a closer response to in vivo physiology observed responses. They are also the best models to understand the complex interactions between different populations of cells and the extracellular matrix, in which tumor-derived EVs modify epithelial or mesenchymal cells to become protumor agents. Finally, the growth of cells in 3D bioreactor-like systems is appointed as the best approach to industrial EVs production, a necessary step toward clinical translation of EVs-based therapy.https://www.mdpi.com/2072-6694/13/2/3073D cultureextracellular vesiclestumoral cellscancertherapy
spellingShingle Guillermo Bordanaba-Florit
Iratxe Madarieta
Beatriz Olalde
Juan M. Falcón-Pérez
Félix Royo
3D Cell Cultures as Prospective Models to Study Extracellular Vesicles in Cancer
Cancers
3D culture
extracellular vesicles
tumoral cells
cancer
therapy
title 3D Cell Cultures as Prospective Models to Study Extracellular Vesicles in Cancer
title_full 3D Cell Cultures as Prospective Models to Study Extracellular Vesicles in Cancer
title_fullStr 3D Cell Cultures as Prospective Models to Study Extracellular Vesicles in Cancer
title_full_unstemmed 3D Cell Cultures as Prospective Models to Study Extracellular Vesicles in Cancer
title_short 3D Cell Cultures as Prospective Models to Study Extracellular Vesicles in Cancer
title_sort 3d cell cultures as prospective models to study extracellular vesicles in cancer
topic 3D culture
extracellular vesicles
tumoral cells
cancer
therapy
url https://www.mdpi.com/2072-6694/13/2/307
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