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A Model for Perineural Invasion in Head and Neck Squamous Cell Carcinoma
Published on: January 5, 2017
MicroRNA-340 inhibits squamous cell carcinoma cell proliferation, migration and invasion by downregulating RhoA
Huina Wang1, Weinan Guo1, Qiang Jian1
1Department of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Background:
MicroRNAs are reported to play an important role in tumor growth and metastasis, including squamous cell carcinoma (SCC). Accumulative evidence has revealed that dysregulated miR-340 expression contributed to the carcinogenesis and development of various cancers.
Objective:
The aim of the current study was to investigate the role and the underlying mechanism of miR-340 in SCC cell proliferation, migration and invasion.
Methods:
Quantitative real-time PCR was performed to examine the expression of miR-340 in SCC tissues and cell lines. The function of miR-340 in SCC was investigated through Cell Counting Kit-8, wound healing, transwell migration and invasion assays. Bioinformatics analysis, luciferase reporter assay, western blotting and immunohistochemical analysis were conducted to predict and confirm the target gene of miR-340.
Results:
In the present study, we first found that miR-340 was significantly decreased in both SCC tissues and cell lines. Moreover, ectopic expression of miR-340 remarkably attenuated SCC cell proliferation, migration and invasion, whereas inhibition of endogenous miR-340 promoted SCC cell proliferation, migration and invasion in vitro. Our subsequent bioinformatics analysis and luciferase reporter assay showed that RhoA was a novel direct target of miR-340 in SCC cells, and the knockdown of RhoA expression rescued the effects of miR-340 inhibition on SCC cell proliferation, migration and invasion. More importantly, the expression of RhoA and miR-340 was negatively correlated in SCC tissues.
Conclusion:
Our findings demonstrate the tumor suppressor role of miR-340 in SCC by directly regulating RhoA. Therefore, restoration of miR-340 expression can be a potential therapeutic approach for SCC treatment.
Insights
MicroRNA-340 (miR-340) acts as a tumor suppressor in squamous cell carcinoma (SCC) by inhibiting cell proliferation, migration, and invasion. This study identifies RhoA as a direct target, suggesting miR-340 restoration as a potential SCC therapy.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- MicroRNAs (miRNAs) are crucial in tumor progression and metastasis, particularly in squamous cell carcinoma (SCC).
- Dysregulated miR-340 expression is implicated in the development of various cancers, including SCC.
Purpose of the Study:
- To elucidate the role and underlying mechanism of miR-340 in SCC cell proliferation, migration, and invasion.
- To identify the direct molecular targets of miR-340 in SCC.
Main Methods:
- Quantitative real-time PCR to assess miR-340 expression in SCC tissues and cell lines.
- In vitro assays (Cell Counting Kit-8, wound healing, transwell) to evaluate miR-340's functional impact.
- Bioinformatics, luciferase reporter assays, western blotting, and immunohistochemistry to identify and validate miR-340 targets.
Main Results:
- miR-340 expression was significantly downregulated in SCC tissues and cell lines.
- Overexpression of miR-340 suppressed SCC cell proliferation, migration, and invasion; conversely, inhibition promoted these processes.
- RhoA was identified as a direct target of miR-340, and its knockdown reversed the effects of miR-340 inhibition.
- A negative correlation was observed between RhoA and miR-340 expression in SCC tissues.
Conclusions:
- miR-340 functions as a tumor suppressor in SCC by directly targeting RhoA.
- Restoring miR-340 expression presents a potential therapeutic strategy for SCC treatment.
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