Laboratory of General Physiology, Department of Biological and Environmental Sciences and Technologies, University of Salento, via Monteroni 73100, Lecce, Italy.
Cancer Lett. 2011 Nov 1;310(1):1-8. doi: 10.1016/j.canlet.2011.04.009. Epub 2011 Jun 24.
Carcinoma progression is associated with the loss of epithelial features, and the acquisition of a mesenchymal phenotype by tumour cells. Herein we show that exposure of MCF-7 cells to epidermal growth factor (EGF) resulted in morphological alterations characteristic of epithelial-to-mesenchymal transition (EMT). EGF treatment resulted in increased motility along with an up-regulation of transcription factors Slug, Zeb1, Zeb2, and mesenchymal markers Vimentin and N-cadherin. Treatment of MCF-7 cells with a combined stimulation of EGF and resveratrol, a naturally occurring stilbene with antitumor properties, failed to alter cell morphology, motility and overexpression of EMT markers induced by EGF. Using specific chemical inhibitors, we demonstrated that EGF-induced EMT is mediated by extracellular signal-regulated kinase 1/2 (ERK 1/2) signalling pathway and that resveratrol is able to repress EGF-induced ERK activation. In summary, these data provide new evidence of the inhibitory effect of resveratrol on EGF-induced EMT cell transformation.
癌细胞的进展与上皮特征的丧失以及肿瘤细胞获得间充质表型有关。本文中,我们发现 MCF-7 细胞暴露于表皮生长因子(EGF)后,会发生具有上皮-间充质转化(EMT)特征的形态改变。EGF 处理会增加细胞的迁移能力,并上调转录因子 Slug、Zeb1、Zeb2 以及间充质标志物波形蛋白和 N-钙黏蛋白。用 EGF 和白藜芦醇(一种具有抗肿瘤特性的天然芪类化合物)联合刺激 MCF-7 细胞,未能改变 EGF 诱导的细胞形态、迁移和 EMT 标志物的过度表达。使用特定的化学抑制剂,我们证明 EGF 诱导的 EMT 是由细胞外信号调节激酶 1/2(ERK 1/2)信号通路介导的,并且白藜芦醇能够抑制 EGF 诱导的 ERK 激活。总之,这些数据为白藜芦醇对 EGF 诱导的 EMT 细胞转化的抑制作用提供了新的证据。