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Tumor-Associated Lymphatic Vessel Features and Immunomodulatory Functions
The lymphatic system comprises a network of lymphoid tissues and vessels that drains the extracellular compartment of most tissues. During tumor development, lymphatic endothelial cells (LECs) substantially expand in response to VEGFR-3 engagement by VEGF-C produced in the tumor microenvironment, a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465591/ https://www.ncbi.nlm.nih.gov/pubmed/31024552 http://dx.doi.org/10.3389/fimmu.2019.00720 |
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author | Garnier, Laure Gkountidi, Anastasia-Olga Hugues, Stephanie |
author_facet | Garnier, Laure Gkountidi, Anastasia-Olga Hugues, Stephanie |
author_sort | Garnier, Laure |
collection | PubMed |
description | The lymphatic system comprises a network of lymphoid tissues and vessels that drains the extracellular compartment of most tissues. During tumor development, lymphatic endothelial cells (LECs) substantially expand in response to VEGFR-3 engagement by VEGF-C produced in the tumor microenvironment, a process known as tumor-associated lymphangiogenesis. Lymphatic drainage from the tumor to the draining lymph nodes consequently increases, powering interstitial flow in the tumor stroma. The ability of a tumor to induce and activate lymphatic growth has been positively correlated with metastasis. Much effort has been made to identify genes responsible for tumor-associated lymphangiogenesis. Inhibition of lymphangiogenesis with soluble VEGFR-3 or with specific monoclonal antibodies decreases tumor spread to LNs in rodent models. Importantly, tumor-associated lymphatics do not only operate as tumor cell transporters but also play critical roles in anti-tumor immunity. Therefore, metastatic as well as primary tumor progression can be affected by manipulating tumor-associated lymphatic remodeling or function. Here, we review and discuss our current knowledge on the contribution of LECs immersed in the tumor microenvironment as immunoregulators, as well as a possible functional remodeling of LECs subsets depending on the organ microenvironment. |
format | Online Article Text |
id | pubmed-6465591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64655912019-04-25 Tumor-Associated Lymphatic Vessel Features and Immunomodulatory Functions Garnier, Laure Gkountidi, Anastasia-Olga Hugues, Stephanie Front Immunol Immunology The lymphatic system comprises a network of lymphoid tissues and vessels that drains the extracellular compartment of most tissues. During tumor development, lymphatic endothelial cells (LECs) substantially expand in response to VEGFR-3 engagement by VEGF-C produced in the tumor microenvironment, a process known as tumor-associated lymphangiogenesis. Lymphatic drainage from the tumor to the draining lymph nodes consequently increases, powering interstitial flow in the tumor stroma. The ability of a tumor to induce and activate lymphatic growth has been positively correlated with metastasis. Much effort has been made to identify genes responsible for tumor-associated lymphangiogenesis. Inhibition of lymphangiogenesis with soluble VEGFR-3 or with specific monoclonal antibodies decreases tumor spread to LNs in rodent models. Importantly, tumor-associated lymphatics do not only operate as tumor cell transporters but also play critical roles in anti-tumor immunity. Therefore, metastatic as well as primary tumor progression can be affected by manipulating tumor-associated lymphatic remodeling or function. Here, we review and discuss our current knowledge on the contribution of LECs immersed in the tumor microenvironment as immunoregulators, as well as a possible functional remodeling of LECs subsets depending on the organ microenvironment. Frontiers Media S.A. 2019-04-09 /pmc/articles/PMC6465591/ /pubmed/31024552 http://dx.doi.org/10.3389/fimmu.2019.00720 Text en Copyright © 2019 Garnier, Gkountidi and Hugues. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Garnier, Laure Gkountidi, Anastasia-Olga Hugues, Stephanie Tumor-Associated Lymphatic Vessel Features and Immunomodulatory Functions |
title | Tumor-Associated Lymphatic Vessel Features and Immunomodulatory Functions |
title_full | Tumor-Associated Lymphatic Vessel Features and Immunomodulatory Functions |
title_fullStr | Tumor-Associated Lymphatic Vessel Features and Immunomodulatory Functions |
title_full_unstemmed | Tumor-Associated Lymphatic Vessel Features and Immunomodulatory Functions |
title_short | Tumor-Associated Lymphatic Vessel Features and Immunomodulatory Functions |
title_sort | tumor-associated lymphatic vessel features and immunomodulatory functions |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465591/ https://www.ncbi.nlm.nih.gov/pubmed/31024552 http://dx.doi.org/10.3389/fimmu.2019.00720 |
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