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Long non-coding RNA TUSC7 acts a molecular sponge for miR-10a and suppresses EMT in hepatocellular carcinoma
Yufeng Wang1, Zhikui Liu1, Bowen Yao1
1Department of Hepatobiliary Surgery, First Affiliated Hospital of Medical College of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China.
Abstract:
Despite advances in the roles of long non-coding RNA (lncRNA) tumor suppressor candidate 7 (TUSC7) in cancer biology, which has been identified as a tumor suppressor by regulating cell proliferation, apoptosis, migration, invasion, cell cycle, and tumor growth, the function of TUSC7 in hepatocellular carcinoma (HCC) remains unknown. In this study, we observed that the expression of TUSC7 was immensely decreased in HCC. Clinically, the lower expression of TUSC7 predicted poorer survival and may be an independent risk factor for HCC patients. Moreover, TUSC7 inhibited cell metastasis, invasion, and epithelial-to-mesenchymal transformation (EMT) through competitively binding miR-10a. Furthermore, we found that TUSC7 could decrease the expression of Eph tyrosine kinase receptor A4 (EphA4), a downstream target of miR-10a as well as an EMT suppressor, through TUSC7-miR-10a-EphA4 axis. Taken together, we demonstrate that TUSC7 suppresses EMT through the TUSC7-miR-10a-EphA4 axis, which may be a potential target for therapeutic intervention in HCC.
Insights
Long non-coding RNA TUSC7 acts as a tumor suppressor in hepatocellular carcinoma (HCC). Its decreased expression correlates with poor survival, and it inhibits cancer progression via the TUSC7-miR-10a-EphA4 axis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long non-coding RNA tumor suppressor candidate 7 (TUSC7) is a known tumor suppressor in various cancers.
- The specific role of TUSC7 in hepatocellular carcinoma (HCC) has not been previously elucidated.
Purpose of the Study:
- To investigate the function and mechanism of TUSC7 in hepatocellular carcinoma (HCC).
- To determine if TUSC7 can serve as a prognostic biomarker or therapeutic target for HCC.
Main Methods:
- Quantitative real-time PCR to assess TUSC7 expression in HCC tissues and cell lines.
- Bioinformatic analysis and luciferase reporter assays to confirm the interaction between TUSC7, miR-10a, and EphA4.
- Cell-based assays to evaluate the effects of TUSC7 on cell migration, invasion, and epithelial-to-mesenchymal transition (EMT).
Main Results:
- TUSC7 expression was significantly downregulated in HCC tissues compared to normal tissues.
- Lower TUSC7 expression was associated with poorer patient survival and identified as an independent risk factor for HCC.
- TUSC7 suppressed HCC cell metastasis, invasion, and EMT by competitively binding to miR-10a.
- TUSC7 downregulated Eph tyrosine kinase receptor A4 (EphA4) expression via the TUSC7-miR-10a-EphA4 axis.
Conclusions:
- TUSC7 functions as a tumor suppressor in HCC by inhibiting EMT through the TUSC7-miR-10a-EphA4 pathway.
- TUSC7 holds potential as a prognostic biomarker and therapeutic target for hepatocellular carcinoma.
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