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Metabolism in tumour-associated macrophages: a quid pro quo with the tumour microenvironment
Lung cancer is the leading cause of death from cancer worldwide. Recent studies demonstrated that the tumour microenvironment (TME) is pivotal for tumour progression, providing multiple targeting opportunities for therapeutic strategies. As one of the most abundant stromal cell types in the TME, tum...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488699/ https://www.ncbi.nlm.nih.gov/pubmed/33004525 http://dx.doi.org/10.1183/16000617.0134-2020 |
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author | Zheng, Xiang Mansouri, Siavash Krager, Annika Grimminger, Friedrich Seeger, Werner Pullamsetti, Soni S. Wheelock, Craig E. Savai, Rajkumar |
author_facet | Zheng, Xiang Mansouri, Siavash Krager, Annika Grimminger, Friedrich Seeger, Werner Pullamsetti, Soni S. Wheelock, Craig E. Savai, Rajkumar |
author_sort | Zheng, Xiang |
collection | PubMed |
description | Lung cancer is the leading cause of death from cancer worldwide. Recent studies demonstrated that the tumour microenvironment (TME) is pivotal for tumour progression, providing multiple targeting opportunities for therapeutic strategies. As one of the most abundant stromal cell types in the TME, tumour-associated macrophages (TAMs) exhibit high plasticity. Malignant cells alter their metabolic profiles to adapt to the limited availability of oxygen and nutrients in the TME, resulting in functional alteration of TAMs. The metabolic features of TAMs are strongly associated with their functional plasticity, which further impacts metabolic profiling in the TME and contributes to tumourigenesis and progression. Here, we review the functional determination of the TME by TAM metabolic alterations, including glycolysis as well as fatty acid and amino acid metabolism, which in turn are influenced by environmental changes. Additionally, we discuss metabolic reprogramming of TAMs to a tumouricidal phenotype as a potential antitumoural therapeutic strategy. |
format | Online Article Text |
id | pubmed-9488699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | European Respiratory Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94886992022-11-14 Metabolism in tumour-associated macrophages: a quid pro quo with the tumour microenvironment Zheng, Xiang Mansouri, Siavash Krager, Annika Grimminger, Friedrich Seeger, Werner Pullamsetti, Soni S. Wheelock, Craig E. Savai, Rajkumar Eur Respir Rev Lung Science Conference Lung cancer is the leading cause of death from cancer worldwide. Recent studies demonstrated that the tumour microenvironment (TME) is pivotal for tumour progression, providing multiple targeting opportunities for therapeutic strategies. As one of the most abundant stromal cell types in the TME, tumour-associated macrophages (TAMs) exhibit high plasticity. Malignant cells alter their metabolic profiles to adapt to the limited availability of oxygen and nutrients in the TME, resulting in functional alteration of TAMs. The metabolic features of TAMs are strongly associated with their functional plasticity, which further impacts metabolic profiling in the TME and contributes to tumourigenesis and progression. Here, we review the functional determination of the TME by TAM metabolic alterations, including glycolysis as well as fatty acid and amino acid metabolism, which in turn are influenced by environmental changes. Additionally, we discuss metabolic reprogramming of TAMs to a tumouricidal phenotype as a potential antitumoural therapeutic strategy. European Respiratory Society 2020-10-01 /pmc/articles/PMC9488699/ /pubmed/33004525 http://dx.doi.org/10.1183/16000617.0134-2020 Text en Copyright ©ERS 2020. https://creativecommons.org/licenses/by-nc/4.0/This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. |
spellingShingle | Lung Science Conference Zheng, Xiang Mansouri, Siavash Krager, Annika Grimminger, Friedrich Seeger, Werner Pullamsetti, Soni S. Wheelock, Craig E. Savai, Rajkumar Metabolism in tumour-associated macrophages: a quid pro quo with the tumour microenvironment |
title | Metabolism in tumour-associated macrophages: a quid pro quo with the tumour microenvironment |
title_full | Metabolism in tumour-associated macrophages: a quid pro quo with the tumour microenvironment |
title_fullStr | Metabolism in tumour-associated macrophages: a quid pro quo with the tumour microenvironment |
title_full_unstemmed | Metabolism in tumour-associated macrophages: a quid pro quo with the tumour microenvironment |
title_short | Metabolism in tumour-associated macrophages: a quid pro quo with the tumour microenvironment |
title_sort | metabolism in tumour-associated macrophages: a quid pro quo with the tumour microenvironment |
topic | Lung Science Conference |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488699/ https://www.ncbi.nlm.nih.gov/pubmed/33004525 http://dx.doi.org/10.1183/16000617.0134-2020 |
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