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Circulating galectin-3 promotes tumor-endothelium-adhesion by upregulating ICAM-1 in endothelium-derived extracellular vesicles
The adhesion of tumor cells to vascular endothelial cells is an important process of tumor metastasis. Studies have shown that tumor could educate vascular endothelial cells to promote tumor metastasis through many ways. However, the effect of tumor cells on the functions of vascular endothelial cel...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642840/ https://www.ncbi.nlm.nih.gov/pubmed/36386163 http://dx.doi.org/10.3389/fphar.2022.979474 |
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author | Wang, Lei Du, Dan-Dan Zheng, Zong-Xue Shang, Peng-Fei Yang, Xiao-Xia Sun, Chao Wang, Xiao-Yan Tang, Ya-Jie Guo, Xiu-Li |
author_facet | Wang, Lei Du, Dan-Dan Zheng, Zong-Xue Shang, Peng-Fei Yang, Xiao-Xia Sun, Chao Wang, Xiao-Yan Tang, Ya-Jie Guo, Xiu-Li |
author_sort | Wang, Lei |
collection | PubMed |
description | The adhesion of tumor cells to vascular endothelial cells is an important process of tumor metastasis. Studies have shown that tumor could educate vascular endothelial cells to promote tumor metastasis through many ways. However, the effect of tumor cells on the functions of vascular endothelial cells-derived extracellular vesicles (H-EVs) and the mechanisms underlying their effects in tumor-endothelium adhesion in metastasis remain mysterious. In this study, we found that H-EVs promoted the adhesion of triple negative breast cancer cell to endothelial cells and cirGal-3 enhanced the adhesion-promoting effects of H-EVs. The underlying mechanism was related to the upregulation of glycolysis in endothelial cells induced by cirGal-3 which led to the increase of the ICAM-1 expression and its transmission to MDA-MB-231 cells by H-EVs. Targeting of cirGal-3 or glycolysis of vascular endothelium in breast cancer therefore represents a promising therapeutic strategy to reduce metastasis. |
format | Online Article Text |
id | pubmed-9642840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96428402022-11-15 Circulating galectin-3 promotes tumor-endothelium-adhesion by upregulating ICAM-1 in endothelium-derived extracellular vesicles Wang, Lei Du, Dan-Dan Zheng, Zong-Xue Shang, Peng-Fei Yang, Xiao-Xia Sun, Chao Wang, Xiao-Yan Tang, Ya-Jie Guo, Xiu-Li Front Pharmacol Pharmacology The adhesion of tumor cells to vascular endothelial cells is an important process of tumor metastasis. Studies have shown that tumor could educate vascular endothelial cells to promote tumor metastasis through many ways. However, the effect of tumor cells on the functions of vascular endothelial cells-derived extracellular vesicles (H-EVs) and the mechanisms underlying their effects in tumor-endothelium adhesion in metastasis remain mysterious. In this study, we found that H-EVs promoted the adhesion of triple negative breast cancer cell to endothelial cells and cirGal-3 enhanced the adhesion-promoting effects of H-EVs. The underlying mechanism was related to the upregulation of glycolysis in endothelial cells induced by cirGal-3 which led to the increase of the ICAM-1 expression and its transmission to MDA-MB-231 cells by H-EVs. Targeting of cirGal-3 or glycolysis of vascular endothelium in breast cancer therefore represents a promising therapeutic strategy to reduce metastasis. Frontiers Media S.A. 2022-10-25 /pmc/articles/PMC9642840/ /pubmed/36386163 http://dx.doi.org/10.3389/fphar.2022.979474 Text en Copyright © 2022 Wang, Du, Zheng, Shang, Yang, Sun, Wang, Tang and Guo. https://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 | Pharmacology Wang, Lei Du, Dan-Dan Zheng, Zong-Xue Shang, Peng-Fei Yang, Xiao-Xia Sun, Chao Wang, Xiao-Yan Tang, Ya-Jie Guo, Xiu-Li Circulating galectin-3 promotes tumor-endothelium-adhesion by upregulating ICAM-1 in endothelium-derived extracellular vesicles |
title | Circulating galectin-3 promotes tumor-endothelium-adhesion by upregulating ICAM-1 in endothelium-derived extracellular vesicles |
title_full | Circulating galectin-3 promotes tumor-endothelium-adhesion by upregulating ICAM-1 in endothelium-derived extracellular vesicles |
title_fullStr | Circulating galectin-3 promotes tumor-endothelium-adhesion by upregulating ICAM-1 in endothelium-derived extracellular vesicles |
title_full_unstemmed | Circulating galectin-3 promotes tumor-endothelium-adhesion by upregulating ICAM-1 in endothelium-derived extracellular vesicles |
title_short | Circulating galectin-3 promotes tumor-endothelium-adhesion by upregulating ICAM-1 in endothelium-derived extracellular vesicles |
title_sort | circulating galectin-3 promotes tumor-endothelium-adhesion by upregulating icam-1 in endothelium-derived extracellular vesicles |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642840/ https://www.ncbi.nlm.nih.gov/pubmed/36386163 http://dx.doi.org/10.3389/fphar.2022.979474 |
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