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Systemic Reprogramming of Endothelial Cell Signaling in Metastasis and Cachexia

Proliferating cancer cells secrete a multitude of factors impacting metabolism, interorgan communication, and tumor progression. The distribution of tumor-derived factors to distant organs occurs via the circulation, which provides an extensive reactive surface lined by endothelial cells. Primary tu...

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Detalles Bibliográficos
Autores principales: Preuss, Stephanie F., Grieshober, Denise, Augustin, Hellmut G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Physiological Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281790/
https://www.ncbi.nlm.nih.gov/pubmed/37222464
http://dx.doi.org/10.1152/physiol.00001.2023
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author Preuss, Stephanie F.
Grieshober, Denise
Augustin, Hellmut G.
author_facet Preuss, Stephanie F.
Grieshober, Denise
Augustin, Hellmut G.
author_sort Preuss, Stephanie F.
collection PubMed
description Proliferating cancer cells secrete a multitude of factors impacting metabolism, interorgan communication, and tumor progression. The distribution of tumor-derived factors to distant organs occurs via the circulation, which provides an extensive reactive surface lined by endothelial cells. Primary tumor-derived proteins impact cancer progression by modulating endothelial cell activation at the (pre-)metastatic niche, which affects tumor cell dissemination as well as the outgrowth of seeded metastatic cells into overt tumors. In addition, new insight indicates that endothelial cell signaling contributes to metabolic symptoms of cancer, including cancer-associated cachexia, opening a new field of vascular metabolism research. This review addresses how tumor-derived factors systemically affect endothelial cell signaling and activation and impact distant organs as well as tumor progression.
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spelling pubmed-102817902023-06-21 Systemic Reprogramming of Endothelial Cell Signaling in Metastasis and Cachexia Preuss, Stephanie F. Grieshober, Denise Augustin, Hellmut G. Physiology (Bethesda) Review Proliferating cancer cells secrete a multitude of factors impacting metabolism, interorgan communication, and tumor progression. The distribution of tumor-derived factors to distant organs occurs via the circulation, which provides an extensive reactive surface lined by endothelial cells. Primary tumor-derived proteins impact cancer progression by modulating endothelial cell activation at the (pre-)metastatic niche, which affects tumor cell dissemination as well as the outgrowth of seeded metastatic cells into overt tumors. In addition, new insight indicates that endothelial cell signaling contributes to metabolic symptoms of cancer, including cancer-associated cachexia, opening a new field of vascular metabolism research. This review addresses how tumor-derived factors systemically affect endothelial cell signaling and activation and impact distant organs as well as tumor progression. American Physiological Society 2023-07-01 2022-07-01 /pmc/articles/PMC10281790/ /pubmed/37222464 http://dx.doi.org/10.1152/physiol.00001.2023 Text en Copyright © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Licensed under Creative Commons Attribution CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/) . Published by the American Physiological Society.
spellingShingle Review
Preuss, Stephanie F.
Grieshober, Denise
Augustin, Hellmut G.
Systemic Reprogramming of Endothelial Cell Signaling in Metastasis and Cachexia
title Systemic Reprogramming of Endothelial Cell Signaling in Metastasis and Cachexia
title_full Systemic Reprogramming of Endothelial Cell Signaling in Metastasis and Cachexia
title_fullStr Systemic Reprogramming of Endothelial Cell Signaling in Metastasis and Cachexia
title_full_unstemmed Systemic Reprogramming of Endothelial Cell Signaling in Metastasis and Cachexia
title_short Systemic Reprogramming of Endothelial Cell Signaling in Metastasis and Cachexia
title_sort systemic reprogramming of endothelial cell signaling in metastasis and cachexia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281790/
https://www.ncbi.nlm.nih.gov/pubmed/37222464
http://dx.doi.org/10.1152/physiol.00001.2023
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