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在体外,NEDD4-1通过CNrasGEF泛素化调节胶质瘤细胞的迁移和侵袭。

NEDD4-1 regulates migration and invasion of glioma cells through CNrasGEF ubiquitination in vitro.

作者信息

Zhang Hao, Nie Wenchen, Zhang Xu, Zhang Gentang, Li Zhiqiang, Wu Huaibing, Shi Qiong, Chen Yong, Ding Zhijun, Zhou Xiuping, Yu Rutong

机构信息

Department of Neurosurgery, Affiliated Hospital of Xuzhou Medical College, Xuzhou, Jiangsu, China ; The Graduate School, Xuzhou Medical College, Xuzhou, Jiangsu, China.

出版信息

PLoS One. 2013 Dec 10;8(12):e82789. doi: 10.1371/journal.pone.0082789. eCollection 2013.

Abstract

Neuronal precursor cell-expressed developmentally down-regulated 4-1 (NEDD4-1) plays a great role in tumor cell growth, but its function and mechanism in cell invasive behavior are totally unknown. Here we report that NEDD4-1 regulates migration and invasion of malignant glioma cells via triggering ubiquitination of cyclic nucleotide Ras guanine nucleotide exchange factor (CNrasGEF) using cultured glioma cells. NEDD4-1 overexpression promoted cell migration and invasion, while its downregulation specifically inhibited them. However, NEDD4-1 did not affect the proliferation and apoptosis of glioma cells. NEDD4-1 physically interacted with CNrasGEF and promoted its poly-ubiquitination and degradation. Contrary to the effect of NEDD4-1, CNrasGEF downregulation promoted cell migration and invasion, while its overexpression inhibited them. Importantly, downregulation of CNrasGEF facilitated the effect of NEDD4-1-induced cell migration and invasion. Interestingly, aberrant up-regulated NEDD4-1 showed reverse correlation with CNrasGEF protein level but not with its mRNA level in glioma tissues. Combined with the in vitro results, the result of glioma tissues indicated post-translationally modification effect of NEDD4-1 on CNrasGEF. Our study suggests that NEDD4-1 regulates cell migration and invasion through ubiquitination of CNrasGEF in vitro.

摘要

神经元前体细胞表达的发育下调蛋白4-1(NEDD4-1)在肿瘤细胞生长中发挥着重要作用,但其在细胞侵袭行为中的功能和机制尚完全未知。在此,我们利用培养的胶质瘤细胞报告称,NEDD4-1通过触发环核苷酸Ras鸟嘌呤核苷酸交换因子(CNrasGEF)的泛素化来调节恶性胶质瘤细胞的迁移和侵袭。NEDD4-1的过表达促进细胞迁移和侵袭,而其下调则特异性地抑制这些过程。然而,NEDD4-1并不影响胶质瘤细胞的增殖和凋亡。NEDD4-1与CNrasGEF发生物理相互作用,并促进其多聚泛素化和降解。与NEDD4-1的作用相反,CNrasGEF的下调促进细胞迁移和侵袭,而其过表达则抑制这些过程。重要的是,CNrasGEF的下调促进了NEDD4-1诱导的细胞迁移和侵袭作用。有趣的是,在胶质瘤组织中,异常上调的NEDD4-1与CNrasGEF蛋白水平呈负相关,而与其mRNA水平无关。结合体外实验结果,胶质瘤组织的结果表明NEDD4-1对CNrasGEF具有翻译后修饰作用。我们的研究表明,NEDD4-1在体外通过对CNrasGEF的泛素化来调节细胞迁移和侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a838/3858320/4629baed07f0/pone.0082789.g001.jpg

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