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Decoding vesicle-based precision oncology in gliomas
Extracellular vesicles (EVs) represent a valuable tool in liquid biopsy with tremendous clinical potential in diagnosis, prognosis, and therapeutic monitoring of gliomas. Compared to tissue biopsy, EV-based liquid biopsy is a low-cost, minimally invasive method that can provide information on tumor...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650467/ https://www.ncbi.nlm.nih.gov/pubmed/36380860 http://dx.doi.org/10.1093/noajnl/vdac035 |
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author | Batool, Syeda Maheen Hsia, Tiffaney Khanna, Sirena K Gamblin, Austin S Rosenfeld, Yulia You, Dong Gil Carter, Bob S Balaj, Leonora |
author_facet | Batool, Syeda Maheen Hsia, Tiffaney Khanna, Sirena K Gamblin, Austin S Rosenfeld, Yulia You, Dong Gil Carter, Bob S Balaj, Leonora |
author_sort | Batool, Syeda Maheen |
collection | PubMed |
description | Extracellular vesicles (EVs) represent a valuable tool in liquid biopsy with tremendous clinical potential in diagnosis, prognosis, and therapeutic monitoring of gliomas. Compared to tissue biopsy, EV-based liquid biopsy is a low-cost, minimally invasive method that can provide information on tumor dynamics before, during, and after treatment. Tumor-derived EVs circulating in biofluids carry a complex cargo of molecular biomarkers, including DNA, RNA, and proteins, which can be indicative of tumor growth and progression. Here, we briefly review current commercial and noncommercial methods for the isolation, quantification, and biochemical characterization of plasma EVs from patients with glioma, touching on whole EV analysis, mutation detection techniques, and genomic and proteomic profiling. We review notable advantages and disadvantages of plasma EV isolation and analytical methods, and we conclude with a discussion on clinical translational opportunities and key challenges associated with the future implementation of EV-based liquid biopsy for glioma treatment. |
format | Online Article Text |
id | pubmed-9650467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96504672022-11-14 Decoding vesicle-based precision oncology in gliomas Batool, Syeda Maheen Hsia, Tiffaney Khanna, Sirena K Gamblin, Austin S Rosenfeld, Yulia You, Dong Gil Carter, Bob S Balaj, Leonora Neurooncol Adv Supplement Articles Extracellular vesicles (EVs) represent a valuable tool in liquid biopsy with tremendous clinical potential in diagnosis, prognosis, and therapeutic monitoring of gliomas. Compared to tissue biopsy, EV-based liquid biopsy is a low-cost, minimally invasive method that can provide information on tumor dynamics before, during, and after treatment. Tumor-derived EVs circulating in biofluids carry a complex cargo of molecular biomarkers, including DNA, RNA, and proteins, which can be indicative of tumor growth and progression. Here, we briefly review current commercial and noncommercial methods for the isolation, quantification, and biochemical characterization of plasma EVs from patients with glioma, touching on whole EV analysis, mutation detection techniques, and genomic and proteomic profiling. We review notable advantages and disadvantages of plasma EV isolation and analytical methods, and we conclude with a discussion on clinical translational opportunities and key challenges associated with the future implementation of EV-based liquid biopsy for glioma treatment. Oxford University Press 2022-11-11 /pmc/articles/PMC9650467/ /pubmed/36380860 http://dx.doi.org/10.1093/noajnl/vdac035 Text en © The Author(s) 2022. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Supplement Articles Batool, Syeda Maheen Hsia, Tiffaney Khanna, Sirena K Gamblin, Austin S Rosenfeld, Yulia You, Dong Gil Carter, Bob S Balaj, Leonora Decoding vesicle-based precision oncology in gliomas |
title | Decoding vesicle-based precision oncology in gliomas |
title_full | Decoding vesicle-based precision oncology in gliomas |
title_fullStr | Decoding vesicle-based precision oncology in gliomas |
title_full_unstemmed | Decoding vesicle-based precision oncology in gliomas |
title_short | Decoding vesicle-based precision oncology in gliomas |
title_sort | decoding vesicle-based precision oncology in gliomas |
topic | Supplement Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650467/ https://www.ncbi.nlm.nih.gov/pubmed/36380860 http://dx.doi.org/10.1093/noajnl/vdac035 |
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