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Baicalein reduces angiogenesis in the inflammatory microenvironment via inhibiting the expression of AP-1

Increasing clinical and experimental studies have demonstrated that refractory chronic inflammation will result in malignant tumor and anti-angiogenic therapy may be an effective way to thwart the progression. Baicalein, one of the major active flavanoids found in Scutellaria baicalensis Georgi, has...

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Autores principales: Huang, Yujie, Miao, Zhaorui, Hu, Yang, Yuan, Yang, Zhou, Yuxin, Wei, Libin, Zhao, Kai, Guo, Qinglong, Lu, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352204/
https://www.ncbi.nlm.nih.gov/pubmed/27903990
http://dx.doi.org/10.18632/oncotarget.13669
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author Huang, Yujie
Miao, Zhaorui
Hu, Yang
Yuan, Yang
Zhou, Yuxin
Wei, Libin
Zhao, Kai
Guo, Qinglong
Lu, Na
author_facet Huang, Yujie
Miao, Zhaorui
Hu, Yang
Yuan, Yang
Zhou, Yuxin
Wei, Libin
Zhao, Kai
Guo, Qinglong
Lu, Na
author_sort Huang, Yujie
collection PubMed
description Increasing clinical and experimental studies have demonstrated that refractory chronic inflammation will result in malignant tumor and anti-angiogenic therapy may be an effective way to thwart the progression. Baicalein, one of the major active flavanoids found in Scutellaria baicalensis Georgi, has been exhibited potent anti-inflammation and anti-tumor effects by reducing angiogenesis. However, the exact mechanism of baicalein on endothelial cells in inflammatory microenvironment was not clear yet. Here, we investigated the anti-angiogenic effect of baicalein by incubating human umbilical vein endothelial cells (HUVECs) with THP-1 conditioned medium in vitro. The tube formation of HUVECs and microvessel outgrowth of rat aorta were attenuated, as well as the number of newly formed blood vessels in chicken chorioallantoic membrane (CAM) was reduced by baicalein. This anti-angiogenic effect was mainly on account of the inhibited motility, migration and invasion of HUVECs. In addition, mechanistic studies showed that baicalein could bind to AP-1 directly and the expression of c-Jun and c-Fos in HUVECs was reduced, accompanied by their increased proteasomal degradation. Besides, baicalein suppressed the nuclear translation, heterodimer formation and DNA binding affinity of c-Jun and c-Fos. What's more, the anti-angiogenic effect of baicalein was further confirmed by matrigel plug assay in vivo. Taken together, our study demonstrated that baicalein could exert its anti-angiogenic effect in the inflammation microenvironment via inhibiting the transcriptional activity of AP-1, which suggested that baicalein might be an alternative treatment against refractory chronic inflammation.
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spelling pubmed-53522042017-04-13 Baicalein reduces angiogenesis in the inflammatory microenvironment via inhibiting the expression of AP-1 Huang, Yujie Miao, Zhaorui Hu, Yang Yuan, Yang Zhou, Yuxin Wei, Libin Zhao, Kai Guo, Qinglong Lu, Na Oncotarget Research Paper Increasing clinical and experimental studies have demonstrated that refractory chronic inflammation will result in malignant tumor and anti-angiogenic therapy may be an effective way to thwart the progression. Baicalein, one of the major active flavanoids found in Scutellaria baicalensis Georgi, has been exhibited potent anti-inflammation and anti-tumor effects by reducing angiogenesis. However, the exact mechanism of baicalein on endothelial cells in inflammatory microenvironment was not clear yet. Here, we investigated the anti-angiogenic effect of baicalein by incubating human umbilical vein endothelial cells (HUVECs) with THP-1 conditioned medium in vitro. The tube formation of HUVECs and microvessel outgrowth of rat aorta were attenuated, as well as the number of newly formed blood vessels in chicken chorioallantoic membrane (CAM) was reduced by baicalein. This anti-angiogenic effect was mainly on account of the inhibited motility, migration and invasion of HUVECs. In addition, mechanistic studies showed that baicalein could bind to AP-1 directly and the expression of c-Jun and c-Fos in HUVECs was reduced, accompanied by their increased proteasomal degradation. Besides, baicalein suppressed the nuclear translation, heterodimer formation and DNA binding affinity of c-Jun and c-Fos. What's more, the anti-angiogenic effect of baicalein was further confirmed by matrigel plug assay in vivo. Taken together, our study demonstrated that baicalein could exert its anti-angiogenic effect in the inflammation microenvironment via inhibiting the transcriptional activity of AP-1, which suggested that baicalein might be an alternative treatment against refractory chronic inflammation. Impact Journals LLC 2016-11-26 /pmc/articles/PMC5352204/ /pubmed/27903990 http://dx.doi.org/10.18632/oncotarget.13669 Text en Copyright: © 2017 Huang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Huang, Yujie
Miao, Zhaorui
Hu, Yang
Yuan, Yang
Zhou, Yuxin
Wei, Libin
Zhao, Kai
Guo, Qinglong
Lu, Na
Baicalein reduces angiogenesis in the inflammatory microenvironment via inhibiting the expression of AP-1
title Baicalein reduces angiogenesis in the inflammatory microenvironment via inhibiting the expression of AP-1
title_full Baicalein reduces angiogenesis in the inflammatory microenvironment via inhibiting the expression of AP-1
title_fullStr Baicalein reduces angiogenesis in the inflammatory microenvironment via inhibiting the expression of AP-1
title_full_unstemmed Baicalein reduces angiogenesis in the inflammatory microenvironment via inhibiting the expression of AP-1
title_short Baicalein reduces angiogenesis in the inflammatory microenvironment via inhibiting the expression of AP-1
title_sort baicalein reduces angiogenesis in the inflammatory microenvironment via inhibiting the expression of ap-1
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352204/
https://www.ncbi.nlm.nih.gov/pubmed/27903990
http://dx.doi.org/10.18632/oncotarget.13669
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