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Updated: Feb 16, 2026

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
MicroRNA-30c functions as a tumor suppressor via targeting SNAI1 in esophageal squamous cell carcinoma
Teng Ma1, Ye Zhao2, Qitong Lu1
1Department of Cardiothoracic Surgery, Zhongda Hospital, Southeast University, Nanjing 210009, China.
Background:
Aberrant expression of miRNAs was involved in tumor initiation, progression and metastasis in multiple cancers. Many kinds of microRNAs in esophageal squamous cell carcinoma (ESCC) have been researched, whereas miR-30c has not been included.
Methods:
Firstly, we explored the expression of miR-30c in ESCC tissue and serum samples and its relations to the survival. To further investigate its effects on ESCC cells, we completed a series of experiments. We detected the effects of ectopic miR-30c expression on the proliferation, migration and invasion of ESCC cells in vitro. We identified the target role of SNAI1 in ESCC using Dual-luciferase reporter assay and western blot assay.
Results:
The results showed miR-30c was significant down-regulated in ESCC tissues and cell lines. Clinically, we found lower miR-30c expression was significantly correlated with worse ESCC progression and survival. Also we clarified that miR-30c suppressed cell proliferation, invasion and epithelial to mesenchymal transition (EMT) of ESCC cell lines. What's more, we figured out that miR-30c inhibits ESCC biological behaviors and EMT progress by directly binding to the 3'-UTR of SNAI1.
Conclusion:
This study provides new insight into the mechanism responsible for the development of human ESCC. Therefore, miR-30c could be a promising biomarker and a therapeutic target for ESCC in the future.
Insights
MicroRNA-30c (miR-30c) is significantly downregulated in esophageal squamous cell carcinoma (ESCC), correlating with poor survival. Restoring miR-30c inhibits ESCC progression and metastasis by targeting SNAI1.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- MicroRNAs (miRNAs) play crucial roles in cancer development.
- Aberrant miRNA expression is implicated in tumor initiation, progression, and metastasis.
- miR-30c's role in esophageal squamous cell carcinoma (ESCC) remained largely unexplored.
Purpose of the Study:
- To investigate the expression and function of miR-30c in ESCC.
- To determine the relationship between miR-30c levels and patient survival.
- To elucidate the molecular mechanism underlying miR-30c's action in ESCC.
Main Methods:
- Expression analysis of miR-30c in ESCC tissues and serum.
- In vitro experiments assessing the impact of miR-30c on ESCC cell proliferation, migration, and invasion.
- Dual-luciferase reporter and Western blot assays to identify miR-30c targets.
Main Results:
- miR-30c was significantly downregulated in ESCC tissues and cell lines.
- Lower miR-30c expression correlated with advanced ESCC progression and poorer survival.
- Ectopic miR-30c expression suppressed ESCC cell proliferation, invasion, and epithelial-to-mesenchymal transition (EMT).
- miR-30c directly targets SNAI1, inhibiting ESCC progression and EMT.
Conclusions:
- miR-30c acts as a tumor suppressor in ESCC.
- miR-30c inhibits ESCC cell proliferation, invasion, and EMT by targeting SNAI1.
- miR-30c represents a potential diagnostic biomarker and therapeutic target for ESCC.
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