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Updated: Jan 30, 2026

Development of Compendium for Esophageal Squamous Cell Carcinoma
Published on: April 12, 2024
miR-34a inhibits esophageal squamous cell carcinoma progression via regulation of FOXM1
Haibo Zhou1, Li Yang2, Xinhua Xu1
1Institute of Oncology, The First College of Clinical Medical Science, Yichang Central People's Hospital Affiliated to China Three Gorges University, Yichang, Hubei 443000, P.R. China.
Abstract:
Downregulation of microRNA-34a (miR-34a) has frequently been observed in esophageal squamous cell carcinoma (ESCC). However, the underlying role and molecular mechanism of miR-34a in ESCC remains largely unknown. In the current study, it was demonstrated that miR-34a was downregulated and forkhead box M1 (FOXM1), a target gene of miR-34a, was upregulated in ESCC tumor tissues. Overexpression of miR-34a decreased FOXM1 mRNA and protein expression in the ESCC cell lines tested (TE-1 and TE-8). Inhibition of miR-34a increased FOXM1 mRNA and protein levels in human esophageal epithelial cells (HEEC). In addition, miR-34a mimics reduced the relative luciferase activity of ESCC cells transfected with FOXM1 3'UTR-WT, but not FOXM1 3'UTR-Mut. The CCK8 assay and scratch wound healing assay showed that overexpression of miR-34a induced inhibition of cell proliferation and cell migration. Additionally, transfection with miR-34a mimics reduced the expression of key genes involved in cell migration (MMP2 and MMP9) in ESCC cells. Thus, the present data demonstrated that miR-34a suppressed ESCC progression by directly targeting FOXM1.
Insights
MicroRNA-34a (miR-34a) suppresses esophageal squamous cell carcinoma (ESCC) progression. This study shows miR-34a targets FOXM1, inhibiting ESCC cell proliferation and migration.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- MicroRNA-34a (miR-34a) is frequently downregulated in esophageal squamous cell carcinoma (ESCC).
- The specific role and molecular mechanisms of miR-34a in ESCC remain largely unelucidated.
- Forkhead box M1 (FOXM1) is a known oncogene and a potential target of miR-34a.
Purpose of the Study:
- To investigate the functional role of miR-34a in ESCC.
- To elucidate the molecular mechanism underlying miR-34a's function in ESCC.
- To determine if miR-34a directly targets FOXM1 in ESCC.
Main Methods:
- Quantitative real-time PCR and Western blotting to assess miR-34a and FOXM1 expression.
- Luciferase reporter assays to validate direct targeting of FOXM1 by miR-34a.
- Cell proliferation (CCK8 assay) and migration (scratch wound healing assay) assays to evaluate miR-34a's functional impact.
Main Results:
- miR-34a was significantly downregulated, while FOXM1 was upregulated in ESCC tissues.
- Overexpression of miR-34a reduced FOXM1 mRNA and protein levels in ESCC cell lines.
- miR-34a directly targeted FOXM1, inhibiting ESCC cell proliferation, migration, and invasion by downregulating MMP2 and MMP9.
Conclusions:
- miR-34a acts as a tumor suppressor in ESCC.
- The miR-34a/FOXM1 axis is a critical regulator of ESCC progression.
- Targeting the miR-34a/FOXM1 pathway may offer a therapeutic strategy for ESCC.
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