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Cancer-secreted exosomal miR-21-5p induces angiogenesis and vascular permeability by targeting KRIT1
Cancer-secreted exosomes are critical mediators of cancer-host crosstalk. In the present study, we showed the delivery of miR-21-5p from colorectal cancer (CRC) cells to endothelial cells via exosomes increased the amount of miR-21-5p in recipient cells. MiR-21-5p suppressed Krev interaction trapped...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178321/ https://www.ncbi.nlm.nih.gov/pubmed/34088891 http://dx.doi.org/10.1038/s41419-021-03803-8 |
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author | He, Qinglian Ye, Aihua Ye, Weibiao Liao, Xiaomin Qin, Guoqiang Xu, Yongqiang Yin, Yuting Luo, Huanqian Yi, Muhua Xian, Liying Zhang, Shihao Qin, Xiyuan Zhu, Wei Li, Yuling |
author_facet | He, Qinglian Ye, Aihua Ye, Weibiao Liao, Xiaomin Qin, Guoqiang Xu, Yongqiang Yin, Yuting Luo, Huanqian Yi, Muhua Xian, Liying Zhang, Shihao Qin, Xiyuan Zhu, Wei Li, Yuling |
author_sort | He, Qinglian |
collection | PubMed |
description | Cancer-secreted exosomes are critical mediators of cancer-host crosstalk. In the present study, we showed the delivery of miR-21-5p from colorectal cancer (CRC) cells to endothelial cells via exosomes increased the amount of miR-21-5p in recipient cells. MiR-21-5p suppressed Krev interaction trapped protein 1 (KRIT1) in recipient HUVECs and subsequently activated β-catenin signaling pathway and increased their downstream targets VEGFa and Ccnd1, which consequently promoted angiogenesis and vascular permeability in CRC. A strong inverse correlation between miR-21-5p and KRIT1 expression levels was observed in CRC-adjacent vessels. Furthermore, miR-21-5p expression in circulating exosomes was markedly higher in CRC patients than in healthy donors. Thus, our data suggest that exosomal miR-21-5p is involved in angiogenesis and vascular permeability in CRC and may be used as a potential new therapeutic target. |
format | Online Article Text |
id | pubmed-8178321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81783212021-06-07 Cancer-secreted exosomal miR-21-5p induces angiogenesis and vascular permeability by targeting KRIT1 He, Qinglian Ye, Aihua Ye, Weibiao Liao, Xiaomin Qin, Guoqiang Xu, Yongqiang Yin, Yuting Luo, Huanqian Yi, Muhua Xian, Liying Zhang, Shihao Qin, Xiyuan Zhu, Wei Li, Yuling Cell Death Dis Article Cancer-secreted exosomes are critical mediators of cancer-host crosstalk. In the present study, we showed the delivery of miR-21-5p from colorectal cancer (CRC) cells to endothelial cells via exosomes increased the amount of miR-21-5p in recipient cells. MiR-21-5p suppressed Krev interaction trapped protein 1 (KRIT1) in recipient HUVECs and subsequently activated β-catenin signaling pathway and increased their downstream targets VEGFa and Ccnd1, which consequently promoted angiogenesis and vascular permeability in CRC. A strong inverse correlation between miR-21-5p and KRIT1 expression levels was observed in CRC-adjacent vessels. Furthermore, miR-21-5p expression in circulating exosomes was markedly higher in CRC patients than in healthy donors. Thus, our data suggest that exosomal miR-21-5p is involved in angiogenesis and vascular permeability in CRC and may be used as a potential new therapeutic target. Nature Publishing Group UK 2021-06-04 /pmc/articles/PMC8178321/ /pubmed/34088891 http://dx.doi.org/10.1038/s41419-021-03803-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article He, Qinglian Ye, Aihua Ye, Weibiao Liao, Xiaomin Qin, Guoqiang Xu, Yongqiang Yin, Yuting Luo, Huanqian Yi, Muhua Xian, Liying Zhang, Shihao Qin, Xiyuan Zhu, Wei Li, Yuling Cancer-secreted exosomal miR-21-5p induces angiogenesis and vascular permeability by targeting KRIT1 |
title | Cancer-secreted exosomal miR-21-5p induces angiogenesis and vascular permeability by targeting KRIT1 |
title_full | Cancer-secreted exosomal miR-21-5p induces angiogenesis and vascular permeability by targeting KRIT1 |
title_fullStr | Cancer-secreted exosomal miR-21-5p induces angiogenesis and vascular permeability by targeting KRIT1 |
title_full_unstemmed | Cancer-secreted exosomal miR-21-5p induces angiogenesis and vascular permeability by targeting KRIT1 |
title_short | Cancer-secreted exosomal miR-21-5p induces angiogenesis and vascular permeability by targeting KRIT1 |
title_sort | cancer-secreted exosomal mir-21-5p induces angiogenesis and vascular permeability by targeting krit1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178321/ https://www.ncbi.nlm.nih.gov/pubmed/34088891 http://dx.doi.org/10.1038/s41419-021-03803-8 |
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