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miR-17-5p and miR-20a-5p suppress postoperative metastasis of hepatocellular carcinoma via blocking HGF/ERBB3-NF-κB
Dong-Li Liu1, Li-Li Lu1, Li-Li Dong1
1Liver Cancer Institute, Zhongshan Hospital, Fudan University, Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai 200032, China.
Abstract:
Dysregulation of microRNA (miRNA) is a frequent event in hepatocellular carcinoma (HCC), but little is known whether it is a bystander or an actual player on residual HCC metastasis during liver microenvironment remodeling initiated by hepatectomy. Methods: The differently expressed miRNAs and mRNAs were identified from RNA-seq data. Western blot, qRT-PCR, fluorescence in situ hybridization, immunofluorescence and immunohistochemical were used to detect the expression of miRNA and mRNA in cell lines and patient tissues. The biological functions were investigated in vitro and in vivo. Chromatin immunoprecipitation, proximity ligation and luciferase reporter assay were used to explore the specific binding of target genes. The expression of HGF/ERBB3 signaling was detected by Western blot. Results: In this study, HGF induced by hepatectomy was shown to promote metastasis of residual HCC cells. miR-17-5p and miR-20a-5p were confirmed to play inhibitory roles on HCC metastasis. And ERBB3 was found to be the common target of miR-17-5p and miR-20a-5p. HCC cells with lower levels of miR-17-5p and miR-20a-5p or higher level of ERBB3 were often more sensitive to response HGF stimuli and to facilitate metastatic colonization both in vitro and in vivo experimental systems. Furthermore, HGF reinforced ERBB3 expression by NF-κB transcriptional activity in a positive feedback loop. Of particular importance, HCC patients with lower levels of miR-17-5p and miR-20a-5p or higher level of ERBB3 had significantly shorter OS and PFS survivals after surgical resection. Conclusion: miR-17-5p and miR-20a-5p could suppress postoperative metastasis of hepatocellular carcinoma via blocking HGF/ERBB3-NF-κB positive feedback loop and offer a new probable strategy for metastasis prevention after HCC resection.
Insights
MicroRNAs miR-17-5p and miR-20a-5p suppress hepatocellular carcinoma (HCC) metastasis by inhibiting the HGF/ERBB3-NF-κB pathway. Lower levels of these miRNAs or higher ERBB3 correlate with poorer patient survival after surgery.
Area of Science:
- Oncology
- Molecular Biology
- Hepatology
Background:
- MicroRNA (miRNA) dysregulation is common in hepatocellular carcinoma (HCC).
- The role of miRNAs in HCC metastasis following hepatectomy remains unclear.
- Liver microenvironment remodeling after surgery can influence residual tumor cells.
Purpose of the Study:
- To investigate the role of specific miRNAs in hepatocellular carcinoma (HCC) metastasis post-hepatectomy.
- To elucidate the molecular mechanisms underlying miRNA-mediated regulation of HCC metastasis.
- To identify potential therapeutic targets for preventing HCC recurrence and metastasis.
Main Methods:
- RNA sequencing to identify differentially expressed miRNAs and mRNAs.
- Quantitative real-time PCR, Western blot, and in situ hybridization for expression analysis.
- In vitro and in vivo functional assays, chromatin immunoprecipitation, and luciferase reporter assays to determine molecular interactions.
Main Results:
- Hepatocyte growth factor (HGF) induced by hepatectomy promotes HCC metastasis.
- miR-17-5p and miR-20a-5p inhibit HCC metastasis by targeting ERBB3.
- A positive feedback loop involving HGF, ERBB3, and NF-κB enhances metastasis; low miR-17-5p/miR-20a-5p or high ERBB3 correlates with shorter patient survival (OS and PFS).
Conclusions:
- miR-17-5p and miR-20a-5p suppress postoperative HCC metastasis by blocking the HGF/ERBB3-NF-κB positive feedback loop.
- These miRNAs represent potential biomarkers for predicting patient outcomes after HCC resection.
- Targeting this pathway offers a novel strategy for preventing metastasis in HCC patients.
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