MiR-4782-3p suppresses glioma migration and invasion by regulating p-cadherin

被引:0
|
作者
Yan, Yan [1 ]
Yan, Hua [1 ]
Liu, Xiao-Zhi [3 ]
Yang, Ping [1 ]
Wang, Qin [1 ]
Zhang, Le [1 ]
Liu, Ying [1 ]
Tang, Hua [2 ]
机构
[1] Tianjin Huan Hu Hosp, Dept Clin Lab, Tianjin Key Lab Cerebral Vasc & Neurodegenerat Di, 6 Jizhao Rd, Tianjin 300350, Peoples R China
[2] Tianjin Med Univ, Sch Basic Med Sci, Dept Microbiol, Tianjin Life Sci Res Ctr, 22 Qixiangtai Rd, Tianjin 300070, Peoples R China
[3] Fifth Cent Hosp, Dept Neurosurg, Tianjin, Peoples R China
关键词
MicroRNA; glioma; p-cadherin; migration; invasion; EPITHELIAL-MESENCHYMAL TRANSITION; RHO-FAMILY GTPASES; P120; CATENIN; BREAST-CANCER; PANCREATIC-CANCER; CELLS; EXPRESSION; ACTIVATION; ADHESION; PROLIFERATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs), a class of non-coding endogenous RNAs, were found to be involved in the regulation of tumor progression with post-transcriptional function. The aim of present study was to explore the role of miR-4782-3p in the development of glioma migration and invasion. Our findings indicated that the expression of miR-4782-3p was significantly repressed in glioma tissues compared to the adjacent normal tissues. In addition, our results demonstrated that miR-4782-3p could suppress the migration and invasion ability of U251 and U87 glioma cells. We also validated P-Cadherin (CDH3) as the potential target gene of miR-4782-3p using an enhanced green fluorescence protein (EGFP) reporter assay. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and Western blot analysis were employed and confirmed that miR-4782-3p suppressed CDH3 mRNA and protein levels. The results suggested that miR-4782-3p could negatively regulate the expression of CDH3 by directly binding to the 3'-UTR of CDH3. We further found that CDH3-dependent cell mobility was associated with p120 catenin (p120ctn) transition from the membrane to the cytoplasm. In conclusion, our findings indicated that a miR-47823p/CDH3/p120ctn pathway was strongly related to the regulation of glioma cell migration and invasion.
引用
收藏
页码:4035 / 4046
页数:12
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