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Role of Tumor-Associated Myeloid Cells in Breast Cancer

Stromal immune cells constitute the tumor microenvironment. These immune cell subsets include myeloid cells, the so-called tumor-associated myeloid cells (TAMCs), which are of two types: tumor-associated macrophages (TAMs) and myeloid-derived suppressor cells (MDSCs). Breast tumors, particularly tho...

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Detalles Bibliográficos
Autores principales: Cha, Yoon Jin, Koo, Ja Seung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464644/
https://www.ncbi.nlm.nih.gov/pubmed/32726950
http://dx.doi.org/10.3390/cells9081785
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author Cha, Yoon Jin
Koo, Ja Seung
author_facet Cha, Yoon Jin
Koo, Ja Seung
author_sort Cha, Yoon Jin
collection PubMed
description Stromal immune cells constitute the tumor microenvironment. These immune cell subsets include myeloid cells, the so-called tumor-associated myeloid cells (TAMCs), which are of two types: tumor-associated macrophages (TAMs) and myeloid-derived suppressor cells (MDSCs). Breast tumors, particularly those in human epidermal growth factor receptor 2 (HER-2)-positive breast cancer and triple-negative breast cancer, are solid tumors containing immune cell stroma. TAMCs drive breast cancer progression via immune mediated, nonimmune-mediated, and metabolic interactions, thus serving as a potential therapeutic target for breast cancer. TAMC-associated breast cancer treatment approaches potentially involve the inhibition of TAM recruitment, modulation of TAM polarization/differentiation, reduction of TAM products, elimination of MDSCs, and reduction of MDSC products. Furthermore, TAMCs can enhance or restore immune responses during cancer immunotherapy. This review describes the role of TAMs and MDSCs in breast cancer and elucidates the clinical implications of TAMs and MDSCs as potential targets for breast cancer treatment.
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spelling pubmed-74646442020-09-04 Role of Tumor-Associated Myeloid Cells in Breast Cancer Cha, Yoon Jin Koo, Ja Seung Cells Review Stromal immune cells constitute the tumor microenvironment. These immune cell subsets include myeloid cells, the so-called tumor-associated myeloid cells (TAMCs), which are of two types: tumor-associated macrophages (TAMs) and myeloid-derived suppressor cells (MDSCs). Breast tumors, particularly those in human epidermal growth factor receptor 2 (HER-2)-positive breast cancer and triple-negative breast cancer, are solid tumors containing immune cell stroma. TAMCs drive breast cancer progression via immune mediated, nonimmune-mediated, and metabolic interactions, thus serving as a potential therapeutic target for breast cancer. TAMC-associated breast cancer treatment approaches potentially involve the inhibition of TAM recruitment, modulation of TAM polarization/differentiation, reduction of TAM products, elimination of MDSCs, and reduction of MDSC products. Furthermore, TAMCs can enhance or restore immune responses during cancer immunotherapy. This review describes the role of TAMs and MDSCs in breast cancer and elucidates the clinical implications of TAMs and MDSCs as potential targets for breast cancer treatment. MDPI 2020-07-27 /pmc/articles/PMC7464644/ /pubmed/32726950 http://dx.doi.org/10.3390/cells9081785 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Cha, Yoon Jin
Koo, Ja Seung
Role of Tumor-Associated Myeloid Cells in Breast Cancer
title Role of Tumor-Associated Myeloid Cells in Breast Cancer
title_full Role of Tumor-Associated Myeloid Cells in Breast Cancer
title_fullStr Role of Tumor-Associated Myeloid Cells in Breast Cancer
title_full_unstemmed Role of Tumor-Associated Myeloid Cells in Breast Cancer
title_short Role of Tumor-Associated Myeloid Cells in Breast Cancer
title_sort role of tumor-associated myeloid cells in breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464644/
https://www.ncbi.nlm.nih.gov/pubmed/32726950
http://dx.doi.org/10.3390/cells9081785
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