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Tumor‐derived microparticles in tumor immunology and immunotherapy
Microvesicles or microparticles, a type of cytoplasm membrane‐derived extracellular vesicles, can be released by cancer cells or normal cell types. Alteration of F‐actin cytoskeleton by various signals may lead to the cytoplasm membrane encapsulating cellular contents to form microparticles, which c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7702100/ https://www.ncbi.nlm.nih.gov/pubmed/32976623 http://dx.doi.org/10.1002/eji.202048548 |
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author | Ma, Jingwei Zhang, Huafeng Tang, Ke Huang, Bo |
author_facet | Ma, Jingwei Zhang, Huafeng Tang, Ke Huang, Bo |
author_sort | Ma, Jingwei |
collection | PubMed |
description | Microvesicles or microparticles, a type of cytoplasm membrane‐derived extracellular vesicles, can be released by cancer cells or normal cell types. Alteration of F‐actin cytoskeleton by various signals may lead to the cytoplasm membrane encapsulating cellular contents to form microparticles, which contain various messenger molecules, including enzymes, RNAs and even DNA fragments, and are released to extracellular space. The release of microparticles by tumor cells (T‐MPs) is a very common event in tumor microenvironments. As a result, T‐MPs not only influence tumor cell biology but also profoundly forge tumor immunology. Moreover, T‐MPs can act as a natural vehicle that delivers therapeutic drugs to tumor cells and immune cells, thus, remodeling tumor microenvironments and resetting antitumor immune responses, thus, conferring T‐MPs a potential role in tumor immunotherapies and tumor vaccines. In this review, we focus on the double‐edged sword role of T‐MPs in tumor immunology, specifically in TAMs and DCs, and emphasize the application of drug‐packaging T‐MPs in cancer patients. We aim to provide a new angle to understand immuno‐oncology and new strategies for cancer immunotherapy. |
format | Online Article Text |
id | pubmed-7702100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77021002020-12-14 Tumor‐derived microparticles in tumor immunology and immunotherapy Ma, Jingwei Zhang, Huafeng Tang, Ke Huang, Bo Eur J Immunol Highlights Microvesicles or microparticles, a type of cytoplasm membrane‐derived extracellular vesicles, can be released by cancer cells or normal cell types. Alteration of F‐actin cytoskeleton by various signals may lead to the cytoplasm membrane encapsulating cellular contents to form microparticles, which contain various messenger molecules, including enzymes, RNAs and even DNA fragments, and are released to extracellular space. The release of microparticles by tumor cells (T‐MPs) is a very common event in tumor microenvironments. As a result, T‐MPs not only influence tumor cell biology but also profoundly forge tumor immunology. Moreover, T‐MPs can act as a natural vehicle that delivers therapeutic drugs to tumor cells and immune cells, thus, remodeling tumor microenvironments and resetting antitumor immune responses, thus, conferring T‐MPs a potential role in tumor immunotherapies and tumor vaccines. In this review, we focus on the double‐edged sword role of T‐MPs in tumor immunology, specifically in TAMs and DCs, and emphasize the application of drug‐packaging T‐MPs in cancer patients. We aim to provide a new angle to understand immuno‐oncology and new strategies for cancer immunotherapy. John Wiley and Sons Inc. 2020-10-28 2020-11 /pmc/articles/PMC7702100/ /pubmed/32976623 http://dx.doi.org/10.1002/eji.202048548 Text en © 2020 The Authors. European Journal of Immunology published by Wiley‐VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Highlights Ma, Jingwei Zhang, Huafeng Tang, Ke Huang, Bo Tumor‐derived microparticles in tumor immunology and immunotherapy |
title | Tumor‐derived microparticles in tumor immunology and immunotherapy |
title_full | Tumor‐derived microparticles in tumor immunology and immunotherapy |
title_fullStr | Tumor‐derived microparticles in tumor immunology and immunotherapy |
title_full_unstemmed | Tumor‐derived microparticles in tumor immunology and immunotherapy |
title_short | Tumor‐derived microparticles in tumor immunology and immunotherapy |
title_sort | tumor‐derived microparticles in tumor immunology and immunotherapy |
topic | Highlights |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7702100/ https://www.ncbi.nlm.nih.gov/pubmed/32976623 http://dx.doi.org/10.1002/eji.202048548 |
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