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Updated: Feb 26, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Overexpression miR-211-5p hinders the proliferation, migration, and invasion of thyroid tumor cells by downregulating
Lei Wang1, Yan-Feng Shen2, Zhi-Min Shi1
1Department of Pathology, Medical College of Hebei University of Engineering, Handan, Hebei Province, China.
Purpose:
This study was aimed to investigate the relationship between miR-211-5p and SOX11, and the effects of their interaction on the proliferation, viability, and invasion of human thyroid cancer (TC) cells.
Methods:
We used quantitative real-time PCR (qRT-PCR) to determine the expression of miR-211-5p and SOX11mRNA in the thyroid tumorous and the adjacent tissues. The target relationship between miR-211-5p and SOX11 was confirmed using dual luciferase reporter gene assay. Flow cytometry, colony formation assay, Transwell assay, and MTT assay were performed to determine the cell-cycle progression, cell apoptosis, proliferation and invasion, respectively. In addition, the tumor formation assay in nude mice was done to assess the effect of miR-211-5p on TC development in vivo.
Results:
MiR-211-5p was underexpressed, whereas SOX11 was overexpressed in TC. The overexpression of miR-211-5p inhibited the expression of SOX11. The cell cycle was arrested and the proliferation as well as invasiveness was suppressed by exogenous miR-211-5p in TC cell line. The antitumor role of miR-211-5p was proved by the animal experiment.
Conclusion:
MiR-211-5p affected the viability, proliferation and invasion of TC by negatively regulating SOX11 expression.
Insights
MicroRNA-211-5p (miR-211-5p) suppresses thyroid cancer (TC) growth by inhibiting SOX11. This study reveals miR-211-5p as a potential therapeutic target for TC, impacting cell viability, proliferation, and invasion.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Thyroid cancer (TC) remains a significant health concern.
- Understanding the molecular mechanisms driving TC progression is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the relationship between microRNA-211-5p (miR-211-5p) and SOX11 in human thyroid cancer (TC) cells.
- To determine the impact of their interaction on TC cell proliferation, viability, and invasion.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) for gene expression analysis.
- Dual luciferase reporter gene assay to confirm target interaction.
- Flow cytometry, colony formation, Transwell, and MTT assays for cellular functions.
- In vivo tumor formation assay in nude mice.
Main Results:
- miR-211-5p was underexpressed, while SOX11 was overexpressed in TC tissues.
- Overexpression of miR-211-5p inhibited SOX11 expression.
- miR-211-5p suppressed TC cell cycle progression, proliferation, and invasion.
- In vivo experiments confirmed the antitumor role of miR-211-5p.
Conclusions:
- miR-211-5p negatively regulates SOX11 expression in TC.
- This interaction significantly affects TC cell viability, proliferation, and invasion.
- miR-211-5p demonstrates potential as a therapeutic agent for thyroid cancer.
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