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Updated: May 10, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
miR-146b-5p inhibits glioma migration and invasion by targeting MMP16
1Dept. of Neuropathology, Tianjin Neurologic Institute, Tianjin Medical University General Hospital, Tianjin 300052, China; Tianjin Key Laboratory of Injuries, Variations and Regeneration of the Nervous System, Tianjin 300052, China; Key Laboratory of Post-trauma Neuro-repair and Regeneration in Central Nervous System, Ministry of Education, Tianjin 300052, China.
Abstract:
miR-146b-5p is frequently down-regulated in solid tumours, including prostate cancer, pancreatic cancer, and glioblastoma. However, the tumour-suppressive effects of miR-146b-5p in malignant gliomas have not been investigated thoroughly. Here, we found that decreased miR-146b-5p expression was strongly correlated with chromosome 10q loss in gliomas, especially glioblastomas. The overexpression of miR-146b-5p in glioblastoma cell lines led to MMP16 mRNA silencing, MMP2 inactivation, and the inhibition of tumour cell migration and invasion. Our results suggest that the restoration of miR-146b-5p expression may be a feasible approach for inhibiting the migration and invasion of malignant gliomas.
Insights
MicroRNA-146b-5p (miR-146b-5p) is often decreased in gliomas, correlating with chromosome 10q loss. Restoring miR-146b-5p inhibits glioblastoma cell migration and invasion by targeting MMP16 and MMP2.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA-146b-5p (miR-146b-5p) is frequently downregulated in various solid tumors.
- Its tumor-suppressive role in malignant gliomas remains underexplored.
- Glioblastomas often exhibit alterations on chromosome 10q.
Purpose of the Study:
- To investigate the role of miR-146b-5p in glioblastoma.
- To explore the correlation between miR-146b-5p expression and chromosome 10q loss in gliomas.
- To determine the impact of miR-146b-5p restoration on glioblastoma cell behavior.
Main Methods:
- Analysis of miR-146b-5p expression levels in gliomas.
- Correlation study with chromosome 10q loss.
- Overexpression of miR-146b-5p in glioblastoma cell lines.
- Assessment of MMP16 mRNA and MMP2 activity.
- Evaluation of tumor cell migration and invasion assays.
Main Results:
- Decreased miR-146b-5p expression strongly correlates with chromosome 10q loss in gliomas, particularly glioblastomas.
- Overexpression of miR-146b-5p resulted in MMP16 mRNA silencing.
- miR-146b-5p restoration led to MMP2 inactivation.
- Inhibition of glioblastoma cell migration and invasion was observed.
Conclusions:
- miR-146b-5p plays a tumor-suppressive role in malignant gliomas.
- Restoring miR-146b-5p expression may be a potential therapeutic strategy.
- Targeting miR-146b-5p could inhibit glioblastoma progression by affecting MMP16 and MMP2 pathways.
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