Overexpression of microRNA-448 inhibits osteosarcoma cell proliferation and invasion through targeting of astrocyte elevated gene-1

被引:15
作者
Jiang, Weibo [1 ]
Wang, Shu [2 ]
Sun, Yang [1 ]
Jiang, Ying [3 ]
Yu, Tao [1 ]
Wang, Jincheng [1 ]
机构
[1] Jilin Univ, Hosp 2, Dept Orthopaed, 218 Ziqiang St, Changchun 130041, Jilin, Peoples R China
[2] Jilin Univ, Hosp 2, Dept Radiotherapy, Changchun 130041, Jilin, Peoples R China
[3] Jilin Univ, Hosp 2, Dept Thyroid Surg, Changchun 130041, Jilin, Peoples R China
关键词
astrocyte elevated gene-1; miR-448; osteosarcoma; cell proliferation; cell invasion; EPITHELIAL-MESENCHYMAL TRANSITION; HEPATOCELLULAR-CARCINOMA; BREAST-CANCER; AEG-1; EXPRESSION; PROMOTES; PROGRESSION; METASTASIS; PATHWAYS; IDENTIFICATION;
D O I
10.3892/mmr.2017.7249
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs/ miRs) have been implicated in the development and progression of osteosarcoma. miR-448 is emerging as a tumor-associated miRNA in many human cancers. However, the role of miR-448 in osteosarcoma remains unknown. The present study aimed to identify the potential role of miR-448 in osteosarcoma. It was demonstrated that miR-448 was significantly downregulated in osteosarcoma cell lines, as detected by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). miR-448 mimics were transfected into osteosarcoma cells to overexpress miR-448. Overexpression of miR-448 markedly inhibited cell proliferation and invasion in osteosarcoma cells. Bioinformatics and luciferase reporter assays demonstrated that astrocyte elevated gene-1 (AEG-1) was a target gene of miR-448. RT-qPCR and western blot analysis revealed that miR-448 inhibited AEG-1 expression. Further data revealed that miR-448 overexpression impeded the Wnt and nuclear factor-kappa B signaling pathways. However, restoration of AEG-1 expression could abolish the miR-448-mediated antitumor effects. Taken together, these findings suggested that miR-448 may inhibit osteosarcoma development by targeting AEG-1, providing a novel candidate miRNA for development of miRNA-targeted therapies for osteosarcoma.
引用
收藏
页码:5713 / 5721
页数:9
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