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Key role of exosomes derived from M2 macrophages in maintaining cancer cell stemness (Review)

Cancer stem cells (CSCs) constitute a specific subset of cells found within tumors that are responsible for initiating, advancing and resisting traditional cancer treatments. M2 macrophages, also known as alternatively activated macrophages, contribute to the development and progression of cancer th...

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Autores principales: Zhang, Weiqiong, Zhou, Ruiping, Liu, Xin, You, Lin, Chen, Chang, Ye, Xiaoling, Liu, Jie, Liang, Youde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10609468/
https://www.ncbi.nlm.nih.gov/pubmed/37711063
http://dx.doi.org/10.3892/ijo.2023.5574
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author Zhang, Weiqiong
Zhou, Ruiping
Liu, Xin
You, Lin
Chen, Chang
Ye, Xiaoling
Liu, Jie
Liang, Youde
author_facet Zhang, Weiqiong
Zhou, Ruiping
Liu, Xin
You, Lin
Chen, Chang
Ye, Xiaoling
Liu, Jie
Liang, Youde
author_sort Zhang, Weiqiong
collection PubMed
description Cancer stem cells (CSCs) constitute a specific subset of cells found within tumors that are responsible for initiating, advancing and resisting traditional cancer treatments. M2 macrophages, also known as alternatively activated macrophages, contribute to the development and progression of cancer through their involvement in promoting angiogenesis, suppressing the immune system, supporting tumor growth and facilitating metastasis. Exosomes, tiny vesicles released by cells, play a crucial role in intercellular communications and have been shown to be associated with cancer development and progression by influencing the immune response; thus, they may serve as markers for diagnosis and prognosis. Currently, investigating the impact of exosomes derived from M2 macrophages on the maintenance of CSCs is a crucial area of research with the aim of developing novel therapeutic strategies to target this process and improve outcomes for individuals with cancer. Understanding the biological functions of exosomes derived from M2 macrophages and their involvement in cancer may lead to the formulation of novel diagnostic tools and treatments for this disease. By targeting M2 macrophages and the exosomes they secrete, promising prospects emerge for cancer treatment, given their substantial contribution to cancer development and progression. Further research is required to fully grasp the intricate interactions between CSCs, M2 macrophages and exosomes in cancer, and to identify fresh targets for cancer therapy. The present review explores the pivotal roles played by exosomes derived from M2 cells in maintaining the stem-like properties of cancer cells.
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spelling pubmed-106094682023-10-28 Key role of exosomes derived from M2 macrophages in maintaining cancer cell stemness (Review) Zhang, Weiqiong Zhou, Ruiping Liu, Xin You, Lin Chen, Chang Ye, Xiaoling Liu, Jie Liang, Youde Int J Oncol Review Cancer stem cells (CSCs) constitute a specific subset of cells found within tumors that are responsible for initiating, advancing and resisting traditional cancer treatments. M2 macrophages, also known as alternatively activated macrophages, contribute to the development and progression of cancer through their involvement in promoting angiogenesis, suppressing the immune system, supporting tumor growth and facilitating metastasis. Exosomes, tiny vesicles released by cells, play a crucial role in intercellular communications and have been shown to be associated with cancer development and progression by influencing the immune response; thus, they may serve as markers for diagnosis and prognosis. Currently, investigating the impact of exosomes derived from M2 macrophages on the maintenance of CSCs is a crucial area of research with the aim of developing novel therapeutic strategies to target this process and improve outcomes for individuals with cancer. Understanding the biological functions of exosomes derived from M2 macrophages and their involvement in cancer may lead to the formulation of novel diagnostic tools and treatments for this disease. By targeting M2 macrophages and the exosomes they secrete, promising prospects emerge for cancer treatment, given their substantial contribution to cancer development and progression. Further research is required to fully grasp the intricate interactions between CSCs, M2 macrophages and exosomes in cancer, and to identify fresh targets for cancer therapy. The present review explores the pivotal roles played by exosomes derived from M2 cells in maintaining the stem-like properties of cancer cells. D.A. Spandidos 2023-09-14 /pmc/articles/PMC10609468/ /pubmed/37711063 http://dx.doi.org/10.3892/ijo.2023.5574 Text en Copyright: © Zhang et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Zhang, Weiqiong
Zhou, Ruiping
Liu, Xin
You, Lin
Chen, Chang
Ye, Xiaoling
Liu, Jie
Liang, Youde
Key role of exosomes derived from M2 macrophages in maintaining cancer cell stemness (Review)
title Key role of exosomes derived from M2 macrophages in maintaining cancer cell stemness (Review)
title_full Key role of exosomes derived from M2 macrophages in maintaining cancer cell stemness (Review)
title_fullStr Key role of exosomes derived from M2 macrophages in maintaining cancer cell stemness (Review)
title_full_unstemmed Key role of exosomes derived from M2 macrophages in maintaining cancer cell stemness (Review)
title_short Key role of exosomes derived from M2 macrophages in maintaining cancer cell stemness (Review)
title_sort key role of exosomes derived from m2 macrophages in maintaining cancer cell stemness (review)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10609468/
https://www.ncbi.nlm.nih.gov/pubmed/37711063
http://dx.doi.org/10.3892/ijo.2023.5574
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