The Role of Tumor-Derived Exosomes (TEX) in Shaping Anti-Tumor Immune Competence
Emerging studies suggest that extracellular vesicles (EVs) mediating intercellular communication in the tumor microenvironment (TME) play a key role in driving cancer progression. Tumor-derived small EVs or exosomes (TEX) enriched in immunosuppressive proteins or in microRNAs targeting suppressive p...
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MDPI AG
2021
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oai:doaj.org-article:6254270982e641faa047dd7003faec5a2021-11-25T17:10:52ZThe Role of Tumor-Derived Exosomes (TEX) in Shaping Anti-Tumor Immune Competence10.3390/cells101130542073-4409https://doaj.org/article/6254270982e641faa047dd7003faec5a2021-11-01T00:00:00Zhttps://www.mdpi.com/2073-4409/10/11/3054https://doaj.org/toc/2073-4409Emerging studies suggest that extracellular vesicles (EVs) mediating intercellular communication in the tumor microenvironment (TME) play a key role in driving cancer progression. Tumor-derived small EVs or exosomes (TEX) enriched in immunosuppressive proteins or in microRNAs targeting suppressive pathways in recipient cells contribute to reprogramming the TME into a cancer-promoting milieu. The adenosinergic pathway is an acknowledged major contributor to tumor-induced immune suppression. TEX carry the components of this pathway and utilize ATP to produce adenosine (ADO). TEX-associated ADO emerges as a key factor in the suppression of T cell responses to therapy. Here, the significance of the ADO pathway in TEX is discussed as a highly effective mechanism of cancer-driven immune cell suppression and of resistance to immune therapies.Theresa L. WhitesideMDPI AGarticletumor-derived exosomes (TEX)extracellular vesicles (EVs)adenosinergic pathwayimmune suppressiontumor microenvironment (TME)Biology (General)QH301-705.5ENCells, Vol 10, Iss 3054, p 3054 (2021) |
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tumor-derived exosomes (TEX) extracellular vesicles (EVs) adenosinergic pathway immune suppression tumor microenvironment (TME) Biology (General) QH301-705.5 |
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tumor-derived exosomes (TEX) extracellular vesicles (EVs) adenosinergic pathway immune suppression tumor microenvironment (TME) Biology (General) QH301-705.5 Theresa L. Whiteside The Role of Tumor-Derived Exosomes (TEX) in Shaping Anti-Tumor Immune Competence |
description |
Emerging studies suggest that extracellular vesicles (EVs) mediating intercellular communication in the tumor microenvironment (TME) play a key role in driving cancer progression. Tumor-derived small EVs or exosomes (TEX) enriched in immunosuppressive proteins or in microRNAs targeting suppressive pathways in recipient cells contribute to reprogramming the TME into a cancer-promoting milieu. The adenosinergic pathway is an acknowledged major contributor to tumor-induced immune suppression. TEX carry the components of this pathway and utilize ATP to produce adenosine (ADO). TEX-associated ADO emerges as a key factor in the suppression of T cell responses to therapy. Here, the significance of the ADO pathway in TEX is discussed as a highly effective mechanism of cancer-driven immune cell suppression and of resistance to immune therapies. |
format |
article |
author |
Theresa L. Whiteside |
author_facet |
Theresa L. Whiteside |
author_sort |
Theresa L. Whiteside |
title |
The Role of Tumor-Derived Exosomes (TEX) in Shaping Anti-Tumor Immune Competence |
title_short |
The Role of Tumor-Derived Exosomes (TEX) in Shaping Anti-Tumor Immune Competence |
title_full |
The Role of Tumor-Derived Exosomes (TEX) in Shaping Anti-Tumor Immune Competence |
title_fullStr |
The Role of Tumor-Derived Exosomes (TEX) in Shaping Anti-Tumor Immune Competence |
title_full_unstemmed |
The Role of Tumor-Derived Exosomes (TEX) in Shaping Anti-Tumor Immune Competence |
title_sort |
role of tumor-derived exosomes (tex) in shaping anti-tumor immune competence |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/6254270982e641faa047dd7003faec5a |
work_keys_str_mv |
AT theresalwhiteside theroleoftumorderivedexosomestexinshapingantitumorimmunecompetence AT theresalwhiteside roleoftumorderivedexosomestexinshapingantitumorimmunecompetence |
_version_ |
1718412653601226752 |