Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1/2 pathway

被引:18
作者
Gentile, Maria Teresa [1 ]
Russo, Rosita [1 ]
Pastorino, Olga [1 ]
Cioffi, Sara [2 ,3 ]
Barbieri, Federica [4 ]
Illingworth, Elisabeth Anne [2 ,3 ]
Grieco, Michele [1 ]
Chambery, Angela [1 ]
Colucci-D'Amato, Luca [1 ]
机构
[1] Univ Campania Luigi Vanvitelli, Dept Environm Biol & Pharmaceut Sci & Technol, Caserta, Italy
[2] Univ Salerno, Dipartimento Chim & Biol Adolfo Zambelli, Salerno, Italy
[3] CNR, Inst Genet & Biophys ABT, Naples, Italy
[4] Univ Genoa, Dept Internal Med, Genoa, Italy
关键词
Endothelial cells; Angiogenesis; Natural compounds; RGWE; ERK signaling; VEGF; GROWTH-FACTOR; CLINICAL-TRIALS; TUBE FORMATION; MARKER NESTIN; ANGIOGENESIS; VEGF; EXPRESSION; MIGRATION; TUMOR; CANCER;
D O I
10.1016/j.yexcr.2018.01.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis is a process encompassing several steps such as endothelial cells proliferation, differentiation and migration to form a vascular network, involving different signal transduction pathways. Among these, ERK1/2 signaling mediates VEGF-dependent signaling pathway. Here we report that the water extract of Ruta graveolens (RGWE), widely known as a medicinal plant, is able to impair in a dose-dependent manner, cell network formation without affecting cell viability. Biochemical analysis showed that the major component of RGWE is rutin, unable to reproduce RGWE effect. We found that RGWE inhibits ERK1/2 phosphorylation and that this event is crucial in cell network formation since the transfection of HUVEC with a constitutively active MEK (caMEK), the ERK1/2 activator, induces a robust cell network formation as compared to untransfected and/or mock transfected cells and, more importantly, caMEK transfected cells became unresponsive to RGWE. Moreover, RGWE inhibits VEGF and nestin gene expression, necessary for vessel formation, and the caMEK transfection induces their higher expression. In conclusion, we report that RGWE is able to significantly impair vessels network formation without affecting cell viability, preventing ERK1/2 activation and, in turn, down-regulating VEGF and nestin expression. These findings point to RGWE as a potential therapeutic tool capable to interfere with pathologic angiogenesis.
引用
收藏
页码:50 / 58
页数:9
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