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Original Research Article | OPEN ACCESS

MicroRNA-16 inhibits the migration and invasion of glioma cell by targeting Bcl-2 gene

Baochang Luo1, Jing Zhang2

1Department of Neurosurgery,; 2Department of Clinical Laboratory, Hanchuan People’s Hospital, Hanchuan City, Hubei Province, China.

For correspondence:-  Jing Zhang   Email: ejkbv6@163.com

Accepted: 2 December 2020        Published: 29 December 2020

Citation: Luo B, Zhang J. MicroRNA-16 inhibits the migration and invasion of glioma cell by targeting Bcl-2 gene. Trop J Pharm Res 2020; 19(12):2499-2504 doi: 10.4314/tjpr.v19i12.3

© 2020 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the effect of microRNA-16 (miR-16) on glioma cell migration and invasiveness, and the mechanism involved.
Methods: MicroRNA-16 mimic or inhibitor was transfected into human glioma (SHG44) cells. Cell migration, invasiveness and morphology were determined using scratch test, Transwell invasion assay, and immunohistochemical staining, respectively. expressions of bcl-2, MMP-9 and MMP-2, and NF-κB1 proteins were measured using Western blotting.   
Results: Overexpression of MicroRNA-16 significantly down-regulated MMP-9 protein in SHG44 cells (p < 0.05), but MMP-2 protein expressions in the 2 groups were comparable (p > 0.05). Protein expressions of MMP-9 and NF-κB1 were significantly down-regulated in human glioma positive cells, relative to negative control.          
Conclusion: MiR-16 overexpression suppresses the migration and invasiveness of SHG44 cells via the regulation of NF-κB1/MMP-9 signaling pathway, and it directly targets bcl-2 gene by inhibiting its protein expression. This finding affords a new target for developing new anti-glioma drugs.

Keywords: Bcl-2, expression, Glioma, MicroRNA-16, NF-?B1signaling pathway

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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