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Immunosuppressive functions of melanoma cell-derived exosomes in plasma of melanoma patients
Tumor-derived exosomes (TEX) are a subset of small extracellular vesicles (sEV) present in all body fluids of patients with cancer. In plasma of patients with metastatic melanoma, numbers of exosomes produced by melanoma cells called MTEX are elevated. To study the role of MTEX in melanoma progressi...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853022/ https://www.ncbi.nlm.nih.gov/pubmed/36684448 http://dx.doi.org/10.3389/fcell.2022.1080925 |
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author | Whiteside, Theresa L. |
author_facet | Whiteside, Theresa L. |
author_sort | Whiteside, Theresa L. |
collection | PubMed |
description | Tumor-derived exosomes (TEX) are a subset of small extracellular vesicles (sEV) present in all body fluids of patients with cancer. In plasma of patients with metastatic melanoma, numbers of exosomes produced by melanoma cells called MTEX are elevated. To study the role of MTEX in melanoma progression, immunoaffinity-based separation of MTEX from total plasma exosomes was performed. The surface of MTEX was decorated by various checkpoint inhibitory proteins, and upon coincubation with immune recipient cells, MTEX suppressed anti-tumor functions of these cells. MTEX emerge as a major mechanism of immune suppression in melanoma and thus might play a role in promoting melanoma progression. |
format | Online Article Text |
id | pubmed-9853022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98530222023-01-21 Immunosuppressive functions of melanoma cell-derived exosomes in plasma of melanoma patients Whiteside, Theresa L. Front Cell Dev Biol Cell and Developmental Biology Tumor-derived exosomes (TEX) are a subset of small extracellular vesicles (sEV) present in all body fluids of patients with cancer. In plasma of patients with metastatic melanoma, numbers of exosomes produced by melanoma cells called MTEX are elevated. To study the role of MTEX in melanoma progression, immunoaffinity-based separation of MTEX from total plasma exosomes was performed. The surface of MTEX was decorated by various checkpoint inhibitory proteins, and upon coincubation with immune recipient cells, MTEX suppressed anti-tumor functions of these cells. MTEX emerge as a major mechanism of immune suppression in melanoma and thus might play a role in promoting melanoma progression. Frontiers Media S.A. 2023-01-06 /pmc/articles/PMC9853022/ /pubmed/36684448 http://dx.doi.org/10.3389/fcell.2022.1080925 Text en Copyright © 2023 Whiteside. https://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(s) 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 Whiteside, Theresa L. Immunosuppressive functions of melanoma cell-derived exosomes in plasma of melanoma patients |
title | Immunosuppressive functions of melanoma cell-derived exosomes in plasma of melanoma patients |
title_full | Immunosuppressive functions of melanoma cell-derived exosomes in plasma of melanoma patients |
title_fullStr | Immunosuppressive functions of melanoma cell-derived exosomes in plasma of melanoma patients |
title_full_unstemmed | Immunosuppressive functions of melanoma cell-derived exosomes in plasma of melanoma patients |
title_short | Immunosuppressive functions of melanoma cell-derived exosomes in plasma of melanoma patients |
title_sort | immunosuppressive functions of melanoma cell-derived exosomes in plasma of melanoma patients |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853022/ https://www.ncbi.nlm.nih.gov/pubmed/36684448 http://dx.doi.org/10.3389/fcell.2022.1080925 |
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