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Updated: May 5, 2026

Modeling Oral-Esophageal Squamous Cell Carcinoma in 3D Organoids
Published on: December 23, 2022
Silencing Dicer expression enhances cellular proliferative and invasive capacities in human tongue squamous cell
Shuguang Zeng1, Jing Yang1, Jianjiang Zhao1
1Stomatological Hospital of Guangdong Province Affiliated to Southern Medical University, Guangzhou, Guangdong 510280, P.R. China.
Abstract:
microRNAs (miRNAs) are aberrantly expressed in cancer. An enzyme essential for miRNA processing is Dicer, whose expression is deregulated in diverse types of cancer and correlates with tumor progression. However, whether the regulation of Dicer expression affects tongue squamous cell carcinoma is unknown. In the present study, we investigated how silencing the expression of Dicer alters cell proliferation, cell cycle patterns, and cell migration and invasion in the Tca-8113 tongue squamous cell carcinoma cell line. Dicer expression levels were determined using quantitative PCR and western blot analysis in normal oral gingival epithelial cells and in two tongue squamous cell carcinoma lines, Tca-8113 and UM-1. Tca-8113 cells were transfected with Dicer siRNA or a negative control siRNA. Cell proliferation was determined using the MTT assay and the cell cycle was examined using flow cytometry. Cell migration and invasion changes were evaluated using wound-healing, adherence and Transwell assays. Dicer was expressed at lower levels in the tongue squamous cell carcinoma cell lines Tca-8113 and UM-1 compared to normal gingival epithelial cells, and less Dicer was expressed in UM-1 cells compared to Tca-8113 cells. Notably, Tca-8113 cells transfected with Dicer siRNA had significantly higher proliferative and invasive abilities than cells transfected with the negative control siRNA or non-transfected cells. Silencing Dicer may promote the progression of tongue squamous cell carcinoma. Dicer could serve a promising biomarker and a potential therapeutic target for tongue squamous cell carcinoma.
Insights
Dicer enzyme levels are lower in tongue squamous cell carcinoma. Silencing Dicer in cancer cells increased proliferation and invasion, suggesting Dicer may inhibit tumor progression.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- MicroRNAs (miRNAs) are crucial in cancer development.
- Dicer, an enzyme vital for miRNA processing, shows altered expression in various cancers, impacting tumor progression.
- The role of Dicer in tongue squamous cell carcinoma (TSCC) remains unclear.
Purpose of the Study:
- To investigate the effect of Dicer silencing on the biological behavior of Tca-8113 tongue squamous cell carcinoma cells.
- To determine Dicer expression levels in normal oral cells and TSCC cell lines.
- To explore Dicer's potential as a biomarker and therapeutic target for TSCC.
Main Methods:
- Quantitative PCR and Western blot to assess Dicer expression in normal and TSCC cell lines (Tca-8113, UM-1).
- Transfection of Tca-8113 cells with Dicer siRNA to silence Dicer expression.
- MTT assay for cell proliferation, flow cytometry for cell cycle analysis.
- Wound-healing, adherence, and Transwell assays for cell migration and invasion.
Main Results:
- Dicer expression was significantly lower in TSCC cell lines (Tca-8113, UM-1) compared to normal oral gingival epithelial cells.
- Tca-8113 cells with silenced Dicer exhibited significantly increased proliferation, migration, and invasion.
- UM-1 cells showed lower Dicer expression than Tca-8113 cells.
Conclusions:
- Reduced Dicer expression correlates with enhanced proliferation and invasion in tongue squamous cell carcinoma.
- Dicer silencing appears to promote TSCC progression.
- Dicer represents a potential diagnostic biomarker and therapeutic target for tongue squamous cell carcinoma.
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