鼻咽癌
罗亚
基因敲除
埃兹林
细胞骨架
生物
细胞生物学
癌症研究
下调和上调
细胞迁移
非翻译区
信使核糖核酸
细胞
细胞培养
基因
信号转导
遗传学
医学
内科学
放射治疗
作者
Chunmei Fan,Hongke Qu,Fang Xiong,Yue Tang,Ting Tang,Lishen Zhang,Yongzhen Mo,Xiayu Li,Can Guo,Shanshan Zhang,Zhaojian Gong,Zheng Li,Bo Xiang,Hao Deng,Ming Zhou,Qianjin Liao,Yujuan Zhou,Xiaoling Li,Yong Li,Guiyuan Li,Fuyan Wang,Zhaoyang Zeng
标识
DOI:10.1016/j.canlet.2020.09.006
摘要
An increasing number of studies have shown that circular RNAs (circRNAs) play important roles in malignant tumor initiation and progression; however, many circRNAs are yet unidentified, and the role of circRNAs in nasopharyngeal carcinoma (NPC) is unclear. Using RNA sequencing, we discovered a novel circRNA, termed circARHGAP12, that was processed from the pre-mRNA of the ARHGAP12 gene. CircARHGAP12 was significantly upregulated in NPC tissues and cell lines and promoted NPC cell migration and invasion. Overexpression or knockdown experiments revealed that circARHGAP12 regulates the expression of cytoskeletal remodeling-related proteins EZR, TPM3, and RhoA. CircARHGAP12 was found to bind directly to the 3′ UTR of EZR mRNA and promote its stability; moreover, EZR protein interacted with TPM3 and RhoA and formed a complex to promote NPC cell invasion and metastasis. This study identified the novel circRNA circARHGAP12, characterized its biological function and mechanism, and increased our understanding of circRNAs in NPC pathogenesis. In particular, circARHGAP12 was found to promote the malignant biological phenotype of NPC via cytoskeletal remodeling, thus providing a clue for targeted therapy of NPC.
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