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Updated: Jun 9, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method
Published on: October 7, 2025
MicroRNA-24 targeting RNA-binding protein DND1 in tongue squamous cell carcinoma
Xiqiang Liu1, Anxun Wang, Caroline E Heidbreder
1Center for Molecular Biology of Oral Diseases, College of Dentistry, University of Illinois at Chicago, Chicago, IL 60612, USA.
Abstract:
Deregulations of microRNA have been frequently observed in tongue squamous cell carcinoma (TSCC), but their roles in tumorigenesis are not entirely clear. Here, we reported the up-regulation of miR-24 in TSCC. MiR-24 up-regulation reduced the expression of RNA-binding protein dead end 1 (DND1). Knockdown of miR-24 led to enhanced expression of DND1. The direct targeting of miR-24 to the DND1 mRNA was predicted bioinformatically and confirmed by luciferase reporter gene assays. Furthermore, the miR-24-mediated change in DND1 expression suppressed the expression of cyclin-dependent kinase inhibitor 1B (CDKN1B), and also led to enhanced proliferation and reduced apoptosis in TSCC cells.
Insights
MicroRNA-24 (miR-24) is upregulated in tongue squamous cell carcinoma (TSCC), reducing dead end 1 (DND1) expression. This impacts cell proliferation and apoptosis, offering potential therapeutic targets for TSCC.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA (miRNA) deregulation is common in tongue squamous cell carcinoma (TSCC), but their specific roles in cancer development remain unclear.
- This study focuses on the role of miR-24 in the context of TSCC tumorigenesis.
Purpose of the Study:
- To investigate the role of miR-24 in tongue squamous cell carcinoma (TSCC).
- To elucidate the molecular mechanisms by which miR-24 influences TSCC progression, including its targets and downstream effects on cell behavior.
Main Methods:
- Bioinformatic prediction and luciferase reporter gene assays were used to confirm the direct targeting of DND1 mRNA by miR-24.
- Experiments involved manipulating miR-24 levels (up-regulation and knockdown) in TSCC cells.
- Cell proliferation and apoptosis assays were performed to assess the functional consequences of altered miR-24 and DND1 expression.
Main Results:
- MiR-24 was found to be up-regulated in TSCC.
- Up-regulation of miR-24 led to decreased expression of the RNA-binding protein dead end 1 (DND1). Conversely, miR-24 knockdown enhanced DND1 expression.
- The miR-24/DND1 axis suppressed cyclin-dependent kinase inhibitor 1B (CDKN1B) expression, resulting in increased proliferation and reduced apoptosis in TSCC cells.
Conclusions:
- MiR-24 acts as an oncogenic microRNA in TSCC by targeting DND1.
- The miR-24/DND1 pathway influences key cellular processes like proliferation and apoptosis in TSCC.
- Targeting the miR-24/DND1 axis may represent a novel therapeutic strategy for tongue squamous cell carcinoma.
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