| Literature DB >> 30972186 |
Tuoye Xu1,2, Wan Yu3, Qingquan Li1, Xiaojian Li4, Yan Shi4, Boqiang Cao1, Yaxuan Zhang1, Seng Wang1, Yan Zhang1, Tianlu Wang1, Baosheng Huang1.
Abstract
In recent years, a large amount of research has reported that microRNA (miRNA) dysregulation is closely related to glioma progression. miR-524, a member of the miRNA family, has been confirmed to be involved in many human diseases, including glioma. However, the role and molecular mechanism of miR-524 in glioma have not been clarified. In our study, we showed that miR-524 expression was significantly decreased in glioma and was associated with glioma recurrence. Next, we performed a series of assays and confirmed that the upregulation of miR-524 suppressed glucose uptake, proliferation, migration and invasion in glioma cell lines. Then, through bioinformatics software and a dual luciferase assay, we demonstrated that NCF2 was a target gene of miR-524. In addition, we found that NCF2 reintroduction restored the inhibitor effect of miR-524 on glioma progression. These results elucidate the mechanism of miR-524 in glioma development and provide a potential therapeutic strategy for glioma patients.Entities:
Keywords: NCF2; glioma; glucose uptake; miR-524
Year: 2019 PMID: 30972186 PMCID: PMC6456563
Source DB: PubMed Journal: Am J Transl Res Impact factor: 4.060