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Updated: Apr 25, 2026

Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
Published on: October 4, 2019
MicroRNA-184 promotes proliferation ability of glioma cells by regulating FOXO3
Qing-Ke Cui1, Wei-Dong Liu2, Jian-Xin Zhu2
1Department of Neurosurgery, The Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P. R. China; Liaocheng People's Hospital, Liaocheng, Shandong, 252000, P. R. China.
Objectives:
To investigate the effect of microRNA (miR-184) on regulating the genesis, development and proliferation of glioma cells.
Methods:
Lipidosome was used to transfect miR-184 mimic and inhibitor to glioma cell line, and the cell proliferation ability changes were determined by MTT and plate cloning experiment after the transfection. WB test was used to measure the levels of cyclinD1, p27 and FOXO3. Meanwhile, QPCR was used to detect miR-184 expression in glioma cell line, glioma tissues and adjacent tissues. Luciferase experiment was used to test 3'UTR gene targeting regulation of miR-184 and FOXO3.
Results:
QPCR results showed a significant lower miR-184 expression level in glioma cell line and glioma tissues than that in juxtacancerous tissue. MTT and plate cloning experiments have shown that after over-expressing of miR-184, the cell proliferation capacity of glioma U87 and T98G was significantly increased, which was significantly inhibited after the inhibition of miR-184. WB results showed a lower expression level of p27 in U87 and T98G cells, and a higher expression level of cyclinD1 after over-expressing of miR-184 was observed. However, a lower expression level of cyclinD1 and a higher expression level of p27 after the inhibition of miR-184. The luciferase activity was inhibited after the over-expressing of miR-184.
Conclusions:
MiR-184 can affect the proliferation abilities of glioma cells and regulate the cell cycle related protein. It plays an important role in the occurrence and development of gliomas.
Insights
MicroRNA-184 (miR-184) plays a crucial role in glioma development. Lower miR-184 levels correlate with increased glioma cell proliferation, impacting cell cycle proteins and tumor growth.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Gliomas are primary brain tumors with complex molecular underpinnings.
- MicroRNAs (miRNAs) are key regulators of gene expression implicated in various cancers.
- Dysregulation of specific miRNAs, like miR-184, may contribute to glioma pathogenesis.
Purpose of the Study:
- To investigate the regulatory role of microRNA-184 (miR-184) in glioma cell genesis, development, and proliferation.
- To elucidate the impact of miR-184 on cell cycle-related proteins in glioma.
Main Methods:
- Transfection of glioma cell lines with miR-184 mimic and inhibitor using lipidosomes.
- Assessment of cell proliferation via MTT and plate cloning assays.
- Western blot (WB) analysis for cyclinD1, p27, and FOXO3 expression.
- Quantitative PCR (QPCR) for miR-184 expression in cell lines and tissues.
- Luciferase reporter assays to confirm direct targeting of FOXO3 by miR-184.
Main Results:
- Significantly lower miR-184 expression was observed in glioma cell lines and tissues compared to adjacent tissues.
- Overexpression of miR-184 increased glioma cell proliferation (U87, T98G), while inhibition decreased it.
- miR-184 modulated cell cycle proteins: increased cyclinD1 and decreased p27 upon overexpression; decreased cyclinD1 and increased p27 upon inhibition.
- Luciferase assays confirmed miR-184 targets the 3'UTR of FOXO3, inhibiting its activity.
Conclusions:
- MicroRNA-184 significantly influences glioma cell proliferation and regulates key cell cycle proteins.
- miR-184 plays a critical role in the occurrence and progression of gliomas.
- These findings highlight miR-184 as a potential therapeutic target for glioma treatment.
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