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Metabolic Reprogramming in Tumor Endothelial Cells
The dynamic crosstalk between the different components of the tumor microenvironment is critical to determine cancer progression, metastatic dissemination, tumor immunity, and therapeutic responses. Angiogenesis is critical for tumor growth, and abnormal blood vessels contribute to hypoxia and acido...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570383/ https://www.ncbi.nlm.nih.gov/pubmed/36232355 http://dx.doi.org/10.3390/ijms231911052 |
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author | García-Caballero, Melissa Sokol, Liliana Cuypers, Anne Carmeliet, Peter |
author_facet | García-Caballero, Melissa Sokol, Liliana Cuypers, Anne Carmeliet, Peter |
author_sort | García-Caballero, Melissa |
collection | PubMed |
description | The dynamic crosstalk between the different components of the tumor microenvironment is critical to determine cancer progression, metastatic dissemination, tumor immunity, and therapeutic responses. Angiogenesis is critical for tumor growth, and abnormal blood vessels contribute to hypoxia and acidosis in the tumor microenvironment. In this hostile environment, cancer and stromal cells have the ability to alter their metabolism in order to support the high energetic demands and favor rapid tumor proliferation. Recent advances have shown that tumor endothelial cell metabolism is reprogrammed, and that targeting endothelial metabolic pathways impacts developmental and pathological vessel sprouting. Therefore, the use of metabolic antiangiogenic therapies to normalize the blood vasculature, in combination with immunotherapies, offers a clinical niche to treat cancer. |
format | Online Article Text |
id | pubmed-9570383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95703832022-10-17 Metabolic Reprogramming in Tumor Endothelial Cells García-Caballero, Melissa Sokol, Liliana Cuypers, Anne Carmeliet, Peter Int J Mol Sci Review The dynamic crosstalk between the different components of the tumor microenvironment is critical to determine cancer progression, metastatic dissemination, tumor immunity, and therapeutic responses. Angiogenesis is critical for tumor growth, and abnormal blood vessels contribute to hypoxia and acidosis in the tumor microenvironment. In this hostile environment, cancer and stromal cells have the ability to alter their metabolism in order to support the high energetic demands and favor rapid tumor proliferation. Recent advances have shown that tumor endothelial cell metabolism is reprogrammed, and that targeting endothelial metabolic pathways impacts developmental and pathological vessel sprouting. Therefore, the use of metabolic antiangiogenic therapies to normalize the blood vasculature, in combination with immunotherapies, offers a clinical niche to treat cancer. MDPI 2022-09-21 /pmc/articles/PMC9570383/ /pubmed/36232355 http://dx.doi.org/10.3390/ijms231911052 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review García-Caballero, Melissa Sokol, Liliana Cuypers, Anne Carmeliet, Peter Metabolic Reprogramming in Tumor Endothelial Cells |
title | Metabolic Reprogramming in Tumor Endothelial Cells |
title_full | Metabolic Reprogramming in Tumor Endothelial Cells |
title_fullStr | Metabolic Reprogramming in Tumor Endothelial Cells |
title_full_unstemmed | Metabolic Reprogramming in Tumor Endothelial Cells |
title_short | Metabolic Reprogramming in Tumor Endothelial Cells |
title_sort | metabolic reprogramming in tumor endothelial cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570383/ https://www.ncbi.nlm.nih.gov/pubmed/36232355 http://dx.doi.org/10.3390/ijms231911052 |
work_keys_str_mv | AT garciacaballeromelissa metabolicreprogrammingintumorendothelialcells AT sokolliliana metabolicreprogrammingintumorendothelialcells AT cuypersanne metabolicreprogrammingintumorendothelialcells AT carmelietpeter metabolicreprogrammingintumorendothelialcells |