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Effect of tumor-associated macrophages on the pyroptosis of breast cancer tumor cells

Macrophages are immune cells with high plasticity that are widely distributed in all tissues and organs of the body. Under the influence of the immune microenvironment of breast tumors, macrophages differentiate into various germline lineages. They exert pro-tumor or tumor-suppressive effects by sec...

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Autores principales: Ji, XuLing, Huang, Xiaoxia, Li, Chao, Guan, Ningning, Pan, Tingting, Dong, Jing, Li, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401873/
https://www.ncbi.nlm.nih.gov/pubmed/37542283
http://dx.doi.org/10.1186/s12964-023-01208-y
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author Ji, XuLing
Huang, Xiaoxia
Li, Chao
Guan, Ningning
Pan, Tingting
Dong, Jing
Li, Lin
author_facet Ji, XuLing
Huang, Xiaoxia
Li, Chao
Guan, Ningning
Pan, Tingting
Dong, Jing
Li, Lin
author_sort Ji, XuLing
collection PubMed
description Macrophages are immune cells with high plasticity that are widely distributed in all tissues and organs of the body. Under the influence of the immune microenvironment of breast tumors, macrophages differentiate into various germline lineages. They exert pro-tumor or tumor-suppressive effects by secreting various cytokines. Pyroptosis is mediated by Gasdermin family proteins, which form holes in cell membranes and cause a violent inflammatory response and cell death. This is an important way for the body to fight off infections. Tumor cell pyroptosis can activate anti-tumor immunity and inhibit tumor growth. At the same time, it releases inflammatory mediators and recruits tumor-associated macrophages (TAMs) for accumulation. Macrophages act as “mediators” of cytokine interactions and indirectly influence the pyroptosis pathway. This paper describes the mechanism of action on the part of TAM in affecting the pyroptosis process of breast tumor cells, as well as its key role in the tumor microenvironment. Additionally, it provides the basis for in-depth research on how to use immune cells to affect breast tumors and guide anti-tumor trends, with important implications for the prevention and treatment of breast tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01208-y.
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spelling pubmed-104018732023-08-05 Effect of tumor-associated macrophages on the pyroptosis of breast cancer tumor cells Ji, XuLing Huang, Xiaoxia Li, Chao Guan, Ningning Pan, Tingting Dong, Jing Li, Lin Cell Commun Signal Review Macrophages are immune cells with high plasticity that are widely distributed in all tissues and organs of the body. Under the influence of the immune microenvironment of breast tumors, macrophages differentiate into various germline lineages. They exert pro-tumor or tumor-suppressive effects by secreting various cytokines. Pyroptosis is mediated by Gasdermin family proteins, which form holes in cell membranes and cause a violent inflammatory response and cell death. This is an important way for the body to fight off infections. Tumor cell pyroptosis can activate anti-tumor immunity and inhibit tumor growth. At the same time, it releases inflammatory mediators and recruits tumor-associated macrophages (TAMs) for accumulation. Macrophages act as “mediators” of cytokine interactions and indirectly influence the pyroptosis pathway. This paper describes the mechanism of action on the part of TAM in affecting the pyroptosis process of breast tumor cells, as well as its key role in the tumor microenvironment. Additionally, it provides the basis for in-depth research on how to use immune cells to affect breast tumors and guide anti-tumor trends, with important implications for the prevention and treatment of breast tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01208-y. BioMed Central 2023-08-04 /pmc/articles/PMC10401873/ /pubmed/37542283 http://dx.doi.org/10.1186/s12964-023-01208-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Ji, XuLing
Huang, Xiaoxia
Li, Chao
Guan, Ningning
Pan, Tingting
Dong, Jing
Li, Lin
Effect of tumor-associated macrophages on the pyroptosis of breast cancer tumor cells
title Effect of tumor-associated macrophages on the pyroptosis of breast cancer tumor cells
title_full Effect of tumor-associated macrophages on the pyroptosis of breast cancer tumor cells
title_fullStr Effect of tumor-associated macrophages on the pyroptosis of breast cancer tumor cells
title_full_unstemmed Effect of tumor-associated macrophages on the pyroptosis of breast cancer tumor cells
title_short Effect of tumor-associated macrophages on the pyroptosis of breast cancer tumor cells
title_sort effect of tumor-associated macrophages on the pyroptosis of breast cancer tumor cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401873/
https://www.ncbi.nlm.nih.gov/pubmed/37542283
http://dx.doi.org/10.1186/s12964-023-01208-y
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