Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zheng, Xiang, Mansouri, Siavash, Krager, Annika, Grimminger, Friedrich, Seeger, Werner, Pullamsetti, Soni S., Wheelock, Craig E., Savai, Rajkumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2020
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
_version_ 1784792716579700736
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
work_keys_str_mv AT zhengxiang metabolismintumourassociatedmacrophagesaquidproquowiththetumourmicroenvironment
AT mansourisiavash metabolismintumourassociatedmacrophagesaquidproquowiththetumourmicroenvironment
AT kragerannika metabolismintumourassociatedmacrophagesaquidproquowiththetumourmicroenvironment
AT grimmingerfriedrich metabolismintumourassociatedmacrophagesaquidproquowiththetumourmicroenvironment
AT seegerwerner metabolismintumourassociatedmacrophagesaquidproquowiththetumourmicroenvironment
AT pullamsettisonis metabolismintumourassociatedmacrophagesaquidproquowiththetumourmicroenvironment
AT wheelockcraige metabolismintumourassociatedmacrophagesaquidproquowiththetumourmicroenvironment
AT savairajkumar metabolismintumourassociatedmacrophagesaquidproquowiththetumourmicroenvironment