MicroRNA-539 inhibits glioma cell proliferation and invasion by targeting DIXDC1

Biomedicine & Pharmacotherapy = Biomédecine & Pharmacothérapie
Junjie QuanLe Zhou

Abstract

Dysregulation of microRNAs (miRNAs) has been suggested to contribute to malignant progression of glioma. Previous studies have demonstrated that miR-539 is dysregulated in malignant progression of cancers. However, the potential role and mechanism of miR-539 in the progression of glioma remains unclear. In this study, we aimed to investigate the expression status and functional significance of miR-539 in glioma. We found that miR-539 expression was significantly decreased in glioma cell lines and tissues. Overexpression of miR-539 markedly inhibited glioma cell proliferation and invasion, while miR-539 suppression exhibited the opposite effect. Bioinformatics analysis and dual-luciferase reporter assays showed that miR-539 directly targeted the 3'-untranslated region of Disheveled-axin domain containing 1 (DIXDC1). DIXDC1 expression was negatively regualted by miR-539 overexpression. An inverse correlation between DIXDC1 mRNA expression and miR-539 expression was found in glioma specimens. Furthermore, knockdown of DIXC1 significantly inhibited proliferation, invasion and Wnt signaling in glioma cells. Overexpression of DIXDC1 partially reversed the inhibitory effect of miR-539 on glioma cell proliferation and invasion. Overall...Continue Reading

Citations

May 29, 2018·Journal of Cellular and Molecular Medicine·Zhiyong XiongYe Yuan
Dec 22, 2017·Journal of Cellular Biochemistry·Xianzheng GaoMingzhi Zhang
Nov 20, 2019·Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire·Fenglin CaiJinhai Tang
Dec 12, 2018·Cancer Biomarkers : Section a of Disease Markers·Hailong SuJuan Meng
Sep 24, 2017·Biomedicine & Pharmacotherapy = Biomédecine & Pharmacothérapie·Dacheng WenShutao Zhao

Related Concepts

S-DIXDC1 protein, human
Brain Tumor, Recurrent
Cell Motility
Mixed Gliomas
Microfilament Proteins
Neoplasm Invasiveness
Signal Transduction
Gene Expression Regulation, Neoplastic
3' Untranslated Regions
RNA, Small Temporal

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