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Updated: Sep 29, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
miR-195 Inhibits Proliferation and Enhances Apoptosis of OSCC Cells via Targeting TLR4
Jianguo Wang1, Renyou Song1, Chunmei Wang1
1Department of Oral and Maxillofacial Surgery, Jiamusi University Affiliated Stomatological Hospital, Jiamusi, China.
Abstract:
The aim of this research was to assess the function of microribonucleic acid (miR)-195 in the apoptosis and proliferation of oral squamous cell carcinoma (OSCC) cells as well as its action mechanism. The downstream target protein of miR-195 was predicted using the biological software. A quantitative polymerase chain reaction (qPCR) was implemented to examine the changes in expressions of miR-195 and its target protein toll-like receptor 4 (TLR4) in OSCC cell lines (TSCCA, Tca8223, Tb3.1, and CAL-27) and normal adult human gingival fibroblasts (HGFs), and the relation between their expressions was assessed. The expressions of phosphorylated proteins in nuclear factor-κB (NF-κB) pathway were determined through western blotting. miR-195 was expressed at a noticeably lower level in four OSCC cells than in HGFs, and the lowest level appeared in CAL-27 cells. Compared with miR-195 control, the miR-195 mimic could obviously raise the expression of miR-195. In CAL-27 cells with high expression of miR-195, the proliferation was inhibited and the apoptosis was evidently enhanced. OSCC cells exhibited evidently reduced protein and mRNA expression of TLR4, and miR-195 expression was inversely associated with TLR4 expression. It was uncovered from the dual-luciferase reporter assay that cells with wild-type TLR4 had prominently weakened luciferase activity relative to cells with mutant-type TLR4, revealing that the direct target of miR-195 is TLR4. The NF-κB pathway was impeded in cells that lowly expressed TLR4. miR-195 blocks the NF-κB pathway via inhibiting the expression of TLR4 in OSCC cells, thereby exerting an antitumor effect.
Insights
MicroRNA-195 (miR-195) suppresses oral squamous cell carcinoma (OSCC) growth by inhibiting toll-like receptor 4 (TLR4) and the NF-κB pathway. This study reveals miR-195 as a potential therapeutic target for OSCC treatment.
Area of Science:
- Molecular Biology
- Oncology
- Gene Regulation
Background:
- Oral squamous cell carcinoma (OSCC) is a prevalent malignancy with complex molecular underpinnings.
- Dysregulation of microRNAs (miRNAs) is implicated in various cancers, including OSCC.
- Understanding the role of specific miRNAs in OSCC pathogenesis is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the functional role of microRNA-195 (miR-195) in the apoptosis and proliferation of oral squamous cell carcinoma (OSCC) cells.
- To elucidate the molecular mechanism by which miR-195 exerts its effects in OSCC.
- To identify the downstream targets of miR-195 involved in OSCC progression.
Main Methods:
- Quantitative polymerase chain reaction (qPCR) to assess miR-195 and toll-like receptor 4 (TLR4) expression in OSCC cell lines and normal cells.
- Western blotting to analyze the expression of phosphorylated proteins in the nuclear factor-κB (NF-κB) pathway.
- Dual-luciferase reporter assay to confirm the direct interaction between miR-195 and TLR4.
Main Results:
- miR-195 expression was significantly downregulated in OSCC cells compared to normal human gingival fibroblasts (HGFs).
- Overexpression of miR-195 inhibited OSCC cell proliferation and promoted apoptosis.
- miR-195 directly targets TLR4, and its downregulation in OSCC leads to increased TLR4 expression and activation of the NF-κB pathway.
Conclusions:
- miR-195 functions as a tumor suppressor in OSCC by inhibiting cell proliferation and inducing apoptosis.
- miR-195 exerts its antitumor effect by downregulating TLR4 expression and subsequently suppressing the NF-κB signaling pathway.
- miR-195 represents a potential therapeutic target for the treatment of oral squamous cell carcinoma.
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