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Cancer-derived exosomal miR-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis

Cancer-derived exosomes are considered a major driver of cancer-induced pre-metastatic niche formation at foreign sites, but the mechanisms remain unclear. Here, we show that miR-25-3p, a metastasis-promoting miRNA of colorectal cancer (CRC), can be transferred from CRC cells to endothelial cells vi...

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Autores principales: Zeng, Zhicheng, Li, Yuling, Pan, Yangjian, Lan, Xiaoliang, Song, Fuyao, Sun, Jingbo, Zhou, Kun, Liu, Xiaolong, Ren, Xiaoli, Wang, Feifei, Hu, Jinlong, Zhu, Xiaohui, Yang, Wei, Liao, Wenting, Li, Guoxin, Ding, Yanqing, Liang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300604/
https://www.ncbi.nlm.nih.gov/pubmed/30568162
http://dx.doi.org/10.1038/s41467-018-07810-w
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author Zeng, Zhicheng
Li, Yuling
Pan, Yangjian
Lan, Xiaoliang
Song, Fuyao
Sun, Jingbo
Zhou, Kun
Liu, Xiaolong
Ren, Xiaoli
Wang, Feifei
Hu, Jinlong
Zhu, Xiaohui
Yang, Wei
Liao, Wenting
Li, Guoxin
Ding, Yanqing
Liang, Li
author_facet Zeng, Zhicheng
Li, Yuling
Pan, Yangjian
Lan, Xiaoliang
Song, Fuyao
Sun, Jingbo
Zhou, Kun
Liu, Xiaolong
Ren, Xiaoli
Wang, Feifei
Hu, Jinlong
Zhu, Xiaohui
Yang, Wei
Liao, Wenting
Li, Guoxin
Ding, Yanqing
Liang, Li
author_sort Zeng, Zhicheng
collection PubMed
description Cancer-derived exosomes are considered a major driver of cancer-induced pre-metastatic niche formation at foreign sites, but the mechanisms remain unclear. Here, we show that miR-25-3p, a metastasis-promoting miRNA of colorectal cancer (CRC), can be transferred from CRC cells to endothelial cells via exosomes. Exosomal miR-25-3p regulates the expression of VEGFR2, ZO-1, occludin and Claudin5 in endothelial cells by targeting KLF2 and KLF4, consequently promotes vascular permeability and angiogenesis. In addition, exosomal miR-25-3p from CRC cells dramatically induces vascular leakiness and enhances CRC metastasis in liver and lung of mice. Moreover, the expression level of miR-25-3p from circulating exosomes is significantly higher in CRC patients with metastasis than those without metastasis. Our work suggests that exosomal miR-25-3p is involved in pre-metastatic niche formation and may be used as a blood-based biomarker for CRC metastasis.
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spelling pubmed-63006042018-12-21 Cancer-derived exosomal miR-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis Zeng, Zhicheng Li, Yuling Pan, Yangjian Lan, Xiaoliang Song, Fuyao Sun, Jingbo Zhou, Kun Liu, Xiaolong Ren, Xiaoli Wang, Feifei Hu, Jinlong Zhu, Xiaohui Yang, Wei Liao, Wenting Li, Guoxin Ding, Yanqing Liang, Li Nat Commun Article Cancer-derived exosomes are considered a major driver of cancer-induced pre-metastatic niche formation at foreign sites, but the mechanisms remain unclear. Here, we show that miR-25-3p, a metastasis-promoting miRNA of colorectal cancer (CRC), can be transferred from CRC cells to endothelial cells via exosomes. Exosomal miR-25-3p regulates the expression of VEGFR2, ZO-1, occludin and Claudin5 in endothelial cells by targeting KLF2 and KLF4, consequently promotes vascular permeability and angiogenesis. In addition, exosomal miR-25-3p from CRC cells dramatically induces vascular leakiness and enhances CRC metastasis in liver and lung of mice. Moreover, the expression level of miR-25-3p from circulating exosomes is significantly higher in CRC patients with metastasis than those without metastasis. Our work suggests that exosomal miR-25-3p is involved in pre-metastatic niche formation and may be used as a blood-based biomarker for CRC metastasis. Nature Publishing Group UK 2018-12-19 /pmc/articles/PMC6300604/ /pubmed/30568162 http://dx.doi.org/10.1038/s41467-018-07810-w Text en © The Author(s) 2018 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/.
spellingShingle Article
Zeng, Zhicheng
Li, Yuling
Pan, Yangjian
Lan, Xiaoliang
Song, Fuyao
Sun, Jingbo
Zhou, Kun
Liu, Xiaolong
Ren, Xiaoli
Wang, Feifei
Hu, Jinlong
Zhu, Xiaohui
Yang, Wei
Liao, Wenting
Li, Guoxin
Ding, Yanqing
Liang, Li
Cancer-derived exosomal miR-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis
title Cancer-derived exosomal miR-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis
title_full Cancer-derived exosomal miR-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis
title_fullStr Cancer-derived exosomal miR-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis
title_full_unstemmed Cancer-derived exosomal miR-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis
title_short Cancer-derived exosomal miR-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis
title_sort cancer-derived exosomal mir-25-3p promotes pre-metastatic niche formation by inducing vascular permeability and angiogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300604/
https://www.ncbi.nlm.nih.gov/pubmed/30568162
http://dx.doi.org/10.1038/s41467-018-07810-w
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