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Updated: Jan 31, 2026

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
MiR-490-3p inhibited the proliferation and metastasis of esophageal squamous cell carcinoma by targeting HMGA2
1Department of Thoracic Surgery, 1st Affiliated Hospital of Anhui Medical University, Hefei, China. zbvz92@163.com.
Objective:
To identify the potential role of miR-490-3p in the development of esophageal squamous cell carcinoma (ESCC), and to explore the possible underlying mechanism.
Patients And Methods:
Human ESCC tissues and cancer-adjacent normal tissues were collected. The mRNA expression level of miR-490-3p was detected by quantitative reverse transcription-polymerase chain reaction (qRT-PCR). On-line target gene prediction software was applied to screen high-mobility group AT-hook 2 (HMGA2). Subsequently, MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide), qRT-PCR, Western blotting, transwell and scratch-wound assays were conducted to analyze the effect of miR-490-3p on the biological function of the ESCC cell line (EC-109).
Results:
In our study, the mRNA expression level of miR-490-3p was remarkably reduced in ESCC tissues and cells. Molecular mechanism analysis confirmed that miR-490-3p could act on the 3'-UTR of HMGA2 and regulate its expression. Subsequent functional experiments indicated that decreased expression of HMGA2 resulting from the up-regulation of miR-490-3p could inhibit the proliferation, invasion, migration and epithelial-mesenchymal transition (EMT) of ESCC cells.
Conclusions:
We discovered the inhibitory effect of miR-490-3p on ESCC by targeting HMGA2, and revealed that miR-490-3p could be a potential therapeutic target for ESCC.
Insights
MicroRNA-490-3p (miR-490-3p) is downregulated in esophageal squamous cell carcinoma (ESCC). Upregulating miR-490-3p inhibits ESCC cell proliferation and metastasis by targeting HMGA2, suggesting its therapeutic potential.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Esophageal squamous cell carcinoma (ESCC) is a significant global health concern.
- MicroRNAs (miRNAs) play crucial roles in cancer development and progression.
- Dysregulation of specific miRNAs can contribute to ESCC pathogenesis.
Purpose of the Study:
- To investigate the role of miR-490-3p in ESCC development.
- To elucidate the underlying molecular mechanism of miR-490-3p in ESCC.
- To explore miR-490-3p as a potential therapeutic target for ESCC.
Main Methods:
- Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) to measure miR-490-3p expression.
- Bioinformatic analysis to predict targets of miR-490-3p, identifying HMGA2.
- In vitro assays including MTT, qRT-PCR, Western blotting, Transwell, and scratch-wound assays to assess functional effects on ESCC cells.
Main Results:
- miR-490-3p expression was significantly reduced in ESCC tissues and cells compared to normal tissues.
- miR-490-3p directly targets the 3'-UTR of HMGA2, regulating its expression.
- Upregulation of miR-490-3p inhibited ESCC cell proliferation, invasion, migration, and epithelial-mesenchymal transition (EMT) by decreasing HMGA2 expression.
Conclusions:
- miR-490-3p exerts an inhibitory effect on ESCC progression.
- The mechanism involves targeting and downregulating HMGA2.
- miR-490-3p represents a promising therapeutic target for esophageal squamous cell carcinoma.
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