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Cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches

Malignancies contain a relatively small number of Mesenchymal stem/stromal cells (MSCs), constituting a crucial tumor microenvironment (TME) component. These cells comprise approximately 0.01–5% of the total TME cell population. MSC differentiation potential and their interaction with the tumor envi...

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Autores principales: Hazrati, Ali, Malekpour, Kosar, Mirsanei, Zahra, Khosrojerdi, Arezou, Rahmani-Kukia, Nasim, Heidari, Neda, Abbasi, Ardeshir, Soudi, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655012/
https://www.ncbi.nlm.nih.gov/pubmed/38022534
http://dx.doi.org/10.3389/fimmu.2023.1280601
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author Hazrati, Ali
Malekpour, Kosar
Mirsanei, Zahra
Khosrojerdi, Arezou
Rahmani-Kukia, Nasim
Heidari, Neda
Abbasi, Ardeshir
Soudi, Sara
author_facet Hazrati, Ali
Malekpour, Kosar
Mirsanei, Zahra
Khosrojerdi, Arezou
Rahmani-Kukia, Nasim
Heidari, Neda
Abbasi, Ardeshir
Soudi, Sara
author_sort Hazrati, Ali
collection PubMed
description Malignancies contain a relatively small number of Mesenchymal stem/stromal cells (MSCs), constituting a crucial tumor microenvironment (TME) component. These cells comprise approximately 0.01–5% of the total TME cell population. MSC differentiation potential and their interaction with the tumor environment enable these cells to affect tumor cells’ growth, immune evasion, metastasis, drug resistance, and angiogenesis. This type of MSC, known as cancer-associated mesenchymal stem/stromal cells (CA-MSCs (interacts with tumor/non-tumor cells in the TME and affects their function by producing cytokines, chemokines, and various growth factors to facilitate tumor cell migration, survival, proliferation, and tumor progression. Considering that the effect of different cells on each other in the TME is a multi-faceted relationship, it is essential to discover the role of these relationships for targeting in tumor therapy. Due to the immunomodulatory role and the tissue repair characteristic of MSCs, these cells can help tumor growth from different aspects. CA-MSCs indirectly suppress antitumor immune response through several mechanisms, including decreasing dendritic cells (DCs) antigen presentation potential, disrupting natural killer (NK) cell differentiation, inducing immunoinhibitory subsets like tumor-associated macrophages (TAMs) and Treg cells, and immune checkpoint expression to reduce effector T cell antitumor responses. Therefore, if these cells can be targeted for treatment so that their population decreases, we can hope for the treatment and improvement of the tumor conditions. Also, various studies show that CA-MSCs in the TME can affect other vital aspects of a tumor, including cell proliferation, drug resistance, angiogenesis, and tumor cell invasion and metastasis. In this review article, we will discuss in detail some of the mechanisms by which CA-MSCs suppress the innate and adaptive immune systems and other mechanisms related to tumor progression.
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spelling pubmed-106550122023-01-01 Cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches Hazrati, Ali Malekpour, Kosar Mirsanei, Zahra Khosrojerdi, Arezou Rahmani-Kukia, Nasim Heidari, Neda Abbasi, Ardeshir Soudi, Sara Front Immunol Immunology Malignancies contain a relatively small number of Mesenchymal stem/stromal cells (MSCs), constituting a crucial tumor microenvironment (TME) component. These cells comprise approximately 0.01–5% of the total TME cell population. MSC differentiation potential and their interaction with the tumor environment enable these cells to affect tumor cells’ growth, immune evasion, metastasis, drug resistance, and angiogenesis. This type of MSC, known as cancer-associated mesenchymal stem/stromal cells (CA-MSCs (interacts with tumor/non-tumor cells in the TME and affects their function by producing cytokines, chemokines, and various growth factors to facilitate tumor cell migration, survival, proliferation, and tumor progression. Considering that the effect of different cells on each other in the TME is a multi-faceted relationship, it is essential to discover the role of these relationships for targeting in tumor therapy. Due to the immunomodulatory role and the tissue repair characteristic of MSCs, these cells can help tumor growth from different aspects. CA-MSCs indirectly suppress antitumor immune response through several mechanisms, including decreasing dendritic cells (DCs) antigen presentation potential, disrupting natural killer (NK) cell differentiation, inducing immunoinhibitory subsets like tumor-associated macrophages (TAMs) and Treg cells, and immune checkpoint expression to reduce effector T cell antitumor responses. Therefore, if these cells can be targeted for treatment so that their population decreases, we can hope for the treatment and improvement of the tumor conditions. Also, various studies show that CA-MSCs in the TME can affect other vital aspects of a tumor, including cell proliferation, drug resistance, angiogenesis, and tumor cell invasion and metastasis. In this review article, we will discuss in detail some of the mechanisms by which CA-MSCs suppress the innate and adaptive immune systems and other mechanisms related to tumor progression. Frontiers Media S.A. 2023-11-03 /pmc/articles/PMC10655012/ /pubmed/38022534 http://dx.doi.org/10.3389/fimmu.2023.1280601 Text en Copyright © 2023 Hazrati, Malekpour, Mirsanei, Khosrojerdi, Rahmani-Kukia, Heidari, Abbasi and Soudi 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 Immunology
Hazrati, Ali
Malekpour, Kosar
Mirsanei, Zahra
Khosrojerdi, Arezou
Rahmani-Kukia, Nasim
Heidari, Neda
Abbasi, Ardeshir
Soudi, Sara
Cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches
title Cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches
title_full Cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches
title_fullStr Cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches
title_full_unstemmed Cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches
title_short Cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches
title_sort cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655012/
https://www.ncbi.nlm.nih.gov/pubmed/38022534
http://dx.doi.org/10.3389/fimmu.2023.1280601
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