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In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNA-346 inhibits the growth of glioma by directly targeting NFIB
Yangyang Li1, Jia Xu1, Jiale Zhang1
1Department of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029 Jiangsu China.
Background:
Glioma is considered one of the most common tumors and has a poor prognosis. Recently, microRNAs (miRNAs) have been reported to be strongly linked to various human tumors including glioma. In this study, we investigated a new anticancer miRNA, miR-346, to determine the effects and mechanism of miR-346 and its downstream target gene NFIB on tumors.
Methods:
Lentivirus transfection, real-time PCR, western blotting, immunohistochemistry, cell proliferation assays, and mouse experiments were used to examine the relationship between miR-346 and its regulation of NFIB in glioma cells.
Results:
The expression of miR-346 was downregulated in glioma cells. Overexpression of miR-346 arrested the cell cycle of glioma cells and inhibited their proliferation in vitro and in vivo. NFIB was a direct target of miR-346, whose expression was reduced by the miRNA. Overexpression of NFIB reversed all tested functions of miR-346.
Conclusion:
miR-346 inhibited the growth of glioma cells by targeting NFIB and may be a new prognostic and diagnostic biomarker for glioma.
Insights
MicroRNA-346 (miR-346) inhibits glioma cell growth by targeting NFIB. This microRNA may serve as a novel biomarker for glioma diagnosis and prognosis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Glioma is a prevalent and aggressive brain tumor with a poor patient prognosis.
- MicroRNAs (miRNAs) play a crucial role in the development and progression of various human cancers, including glioma.
Purpose of the Study:
- To investigate the potential anticancer role of a novel microRNA, miR-346, in glioma.
- To elucidate the mechanism by which miR-346 affects glioma growth, focusing on its downstream target gene, NFIB.
Main Methods:
- Utilized lentivirus transfection for gene manipulation in glioma cells.
- Employed real-time PCR and western blotting to assess gene and protein expression levels.
- Conducted cell proliferation assays and in vivo mouse experiments to evaluate functional effects.
- Performed immunohistochemistry to analyze protein localization and expression.
Main Results:
- miR-346 expression was found to be significantly downregulated in glioma cells.
- Overexpression of miR-346 led to cell cycle arrest and inhibited glioma cell proliferation both in vitro and in vivo.
- NFIB was identified as a direct target of miR-346, with its expression being suppressed by the miRNA.
- Restoration of NFIB expression counteracted the tumor-suppressive effects of miR-346.
Conclusions:
- miR-346 effectively inhibits glioma cell growth through the direct targeting of NFIB.
- miR-346 holds promise as a potential novel biomarker for glioma diagnosis and prognosis.
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