Delgado-Bellido Daniel, Bueno-Galera Concepción, López-Jiménez Laura, Garcia-Diaz Angel, Oliver F Javier
Instituto de Parasitología y Biomedicina López Neyra, CSIC, CIBERONC, Granada, Spain.
Front Oncol. 2020 Jan 24;10:18. doi: 10.3389/fonc.2020.00018. eCollection 2020.
Aberrant extra-vascular expression of VE-cadherin has been observed in metastasis associated with Vasculogenic Mimicry (VM); we have recently shown that in VM prone cells VE-cadherin is mainly in the form of phospho-VE-cadherin in Y658 allowing increased plasticity that potentiates VM development in malignant cells. In the current study, we present results to show that human malignant melanoma cells VM+, express the VE-cadherin phosphatase VE-PTP. VE-PTP forms a complex with VE-Cadherin and p120-catenin and the presence of this complex act as a safeguard to prevent VE-Cadherin protein degradation by autophagy. Indeed, VE-PTP silencing results in complete degradation of VE-cadherin with the features of autophagy. In summary, this study shows that VE-PTP is involved in VM formation and disruption of VE-PTP/VE-Cadherin/p120 complex results in enhanced autophagy in aggressive VM cells. Thus, we identify VE-PTP as a key player in VM development by regulating VE-cadherin protein degradation through autophagy.
在与血管生成拟态(VM)相关的转移过程中,已观察到VE-钙黏蛋白的异常血管外表达;我们最近发现,在易于形成VM的细胞中,VE-钙黏蛋白主要以Y658位点磷酸化的形式存在,这使得可塑性增加,从而增强了恶性细胞中VM的形成。在本研究中,我们展示的结果表明,VM阳性的人类恶性黑色素瘤细胞表达VE-钙黏蛋白磷酸酶VE-PTP。VE-PTP与VE-钙黏蛋白和p120-连环蛋白形成复合物,该复合物的存在可作为一种保护机制,防止VE-钙黏蛋白通过自噬发生蛋白降解。事实上,VE-PTP沉默会导致具有自噬特征的VE-钙黏蛋白完全降解。总之,本研究表明VE-PTP参与VM的形成,VE-PTP/VE-钙黏蛋白/p120复合物的破坏会导致侵袭性VM细胞中的自噬增强。因此,我们确定VE-PTP是VM发展中的关键因子,它通过自噬调节VE-钙黏蛋白的蛋白降解。