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Metabolic Cancer-Macrophage Crosstalk in the Tumor Microenvironment
SIMPLE SUMMARY: Tumors often include many immune cells that are theoretically able to combat tumor growth. Yet, tumors can induce immune functions that support tumor growth via different routes. In this review, we discuss how cancer cell metabolism regulates the activity of macrophages within tumors...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694986/ https://www.ncbi.nlm.nih.gov/pubmed/33171762 http://dx.doi.org/10.3390/biology9110380 |
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author | de Goede, Kyra E. Driessen, Amber J. M. Van den Bossche, Jan |
author_facet | de Goede, Kyra E. Driessen, Amber J. M. Van den Bossche, Jan |
author_sort | de Goede, Kyra E. |
collection | PubMed |
description | SIMPLE SUMMARY: Tumors often include many immune cells that are theoretically able to combat tumor growth. Yet, tumors can induce immune functions that support tumor growth via different routes. In this review, we discuss how cancer cell metabolism regulates the activity of macrophages within tumors and how this affects tumor progression. This is particularly relevant as metabolic pathways in both cancer and immune cells can serve as targets to improve cancer treatment. ABSTRACT: Tumors consist of a wide variety of cells, including immune cells, that affect tumor progression. Macrophages are abundant innate immune cells in the tumor microenvironment (TME) and are crucial in regulating tumorigenicity. Specific metabolic conditions in the TME can alter the phenotype of tumor-associated macrophages (TAMs) in a direction that supports their pro-tumor functions. One of these conditions is the accumulation of metabolites, also known as oncometabolites. Interactions of oncometabolites with TAMs can promote a pro-tumorigenic phenotype, thereby sustaining cancer cell growth and decreasing the chance of eradication. This review focuses on the metabolic cancer-macrophage crosstalk in the TME. We discuss how cancer cell metabolism and oncometabolites affect macrophage phenotype and function, and conversely how macrophage metabolism can impact tumor progression. Lastly, we propose tumor-secreted exosome-mediated metabolic signaling as a potential factor in tumorigenesis. Insight in these processes may contribute to the development of novel cancer therapies. |
format | Online Article Text |
id | pubmed-7694986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76949862020-11-28 Metabolic Cancer-Macrophage Crosstalk in the Tumor Microenvironment de Goede, Kyra E. Driessen, Amber J. M. Van den Bossche, Jan Biology (Basel) Review SIMPLE SUMMARY: Tumors often include many immune cells that are theoretically able to combat tumor growth. Yet, tumors can induce immune functions that support tumor growth via different routes. In this review, we discuss how cancer cell metabolism regulates the activity of macrophages within tumors and how this affects tumor progression. This is particularly relevant as metabolic pathways in both cancer and immune cells can serve as targets to improve cancer treatment. ABSTRACT: Tumors consist of a wide variety of cells, including immune cells, that affect tumor progression. Macrophages are abundant innate immune cells in the tumor microenvironment (TME) and are crucial in regulating tumorigenicity. Specific metabolic conditions in the TME can alter the phenotype of tumor-associated macrophages (TAMs) in a direction that supports their pro-tumor functions. One of these conditions is the accumulation of metabolites, also known as oncometabolites. Interactions of oncometabolites with TAMs can promote a pro-tumorigenic phenotype, thereby sustaining cancer cell growth and decreasing the chance of eradication. This review focuses on the metabolic cancer-macrophage crosstalk in the TME. We discuss how cancer cell metabolism and oncometabolites affect macrophage phenotype and function, and conversely how macrophage metabolism can impact tumor progression. Lastly, we propose tumor-secreted exosome-mediated metabolic signaling as a potential factor in tumorigenesis. Insight in these processes may contribute to the development of novel cancer therapies. MDPI 2020-11-07 /pmc/articles/PMC7694986/ /pubmed/33171762 http://dx.doi.org/10.3390/biology9110380 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 de Goede, Kyra E. Driessen, Amber J. M. Van den Bossche, Jan Metabolic Cancer-Macrophage Crosstalk in the Tumor Microenvironment |
title | Metabolic Cancer-Macrophage Crosstalk in the Tumor Microenvironment |
title_full | Metabolic Cancer-Macrophage Crosstalk in the Tumor Microenvironment |
title_fullStr | Metabolic Cancer-Macrophage Crosstalk in the Tumor Microenvironment |
title_full_unstemmed | Metabolic Cancer-Macrophage Crosstalk in the Tumor Microenvironment |
title_short | Metabolic Cancer-Macrophage Crosstalk in the Tumor Microenvironment |
title_sort | metabolic cancer-macrophage crosstalk in the tumor microenvironment |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694986/ https://www.ncbi.nlm.nih.gov/pubmed/33171762 http://dx.doi.org/10.3390/biology9110380 |
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