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Exosomal microRNAs shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies
Extracellular vesicles secreted by tumor microenvironment (TME) cells are vital players in tumor progression through transferring nucleic acids and proteins. Macrophages are the main immune cells in TME and tumor associated macrophages (TAM) express M2 phenotype, which induce tumor proliferation, an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109313/ https://www.ncbi.nlm.nih.gov/pubmed/35578228 http://dx.doi.org/10.1186/s12935-022-02594-y |
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author | Xu, Wen-Xiu Wang, Dan-Dan Zhao, Zhi-Qiang Zhang, He-Da Yang, Su-Jin Zhang, Qian Li, Lei Zhang, Jian |
author_facet | Xu, Wen-Xiu Wang, Dan-Dan Zhao, Zhi-Qiang Zhang, He-Da Yang, Su-Jin Zhang, Qian Li, Lei Zhang, Jian |
author_sort | Xu, Wen-Xiu |
collection | PubMed |
description | Extracellular vesicles secreted by tumor microenvironment (TME) cells are vital players in tumor progression through transferring nucleic acids and proteins. Macrophages are the main immune cells in TME and tumor associated macrophages (TAM) express M2 phenotype, which induce tumor proliferation, angiogenesis, invasion, metastasis and immune elimination, resulting in the subsequent evolution of malignancies. There are a high number of studies confirmed that tumor cells and TAM interact with each other through extracellular vesicles in various cancers, like pancreatic ductal adenocarcinoma, gastric cancer, breast cancer, ovarian cancer, colon cancer, glioblastoma, hepatocellular cancer, and lung cancer. Herein, this review summarizes the current knowledge on mechanisms of communications between tumor cells and TAM via extracellular vesicles, mainly about microRNAs, and targeting these events might represent a novel approach in the clinical implications of this knowledge into successful anti-cancer strategies. |
format | Online Article Text |
id | pubmed-9109313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91093132022-05-17 Exosomal microRNAs shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies Xu, Wen-Xiu Wang, Dan-Dan Zhao, Zhi-Qiang Zhang, He-Da Yang, Su-Jin Zhang, Qian Li, Lei Zhang, Jian Cancer Cell Int Review Extracellular vesicles secreted by tumor microenvironment (TME) cells are vital players in tumor progression through transferring nucleic acids and proteins. Macrophages are the main immune cells in TME and tumor associated macrophages (TAM) express M2 phenotype, which induce tumor proliferation, angiogenesis, invasion, metastasis and immune elimination, resulting in the subsequent evolution of malignancies. There are a high number of studies confirmed that tumor cells and TAM interact with each other through extracellular vesicles in various cancers, like pancreatic ductal adenocarcinoma, gastric cancer, breast cancer, ovarian cancer, colon cancer, glioblastoma, hepatocellular cancer, and lung cancer. Herein, this review summarizes the current knowledge on mechanisms of communications between tumor cells and TAM via extracellular vesicles, mainly about microRNAs, and targeting these events might represent a novel approach in the clinical implications of this knowledge into successful anti-cancer strategies. BioMed Central 2022-05-16 /pmc/articles/PMC9109313/ /pubmed/35578228 http://dx.doi.org/10.1186/s12935-022-02594-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Xu, Wen-Xiu Wang, Dan-Dan Zhao, Zhi-Qiang Zhang, He-Da Yang, Su-Jin Zhang, Qian Li, Lei Zhang, Jian Exosomal microRNAs shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies |
title | Exosomal microRNAs shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies |
title_full | Exosomal microRNAs shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies |
title_fullStr | Exosomal microRNAs shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies |
title_full_unstemmed | Exosomal microRNAs shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies |
title_short | Exosomal microRNAs shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies |
title_sort | exosomal micrornas shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109313/ https://www.ncbi.nlm.nih.gov/pubmed/35578228 http://dx.doi.org/10.1186/s12935-022-02594-y |
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