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Long Non-coding RNA TUSC7, a Target of miR-23b, Plays Tumor-Suppressing Roles in Human Gliomas
Chao Shang1, Yan Guo2, Yang Hong3
1Department of Neurobiology, College of Basic Medical Sciences, China Medical University Shenyang, China.
Abstract:
Tumour suppressor candidate 7 (TUSC7) is a novel tumor suppressor gene generating long non-coding RNA (lncRNAs) in several types of human cancers. The expression and function of TUSC7 in human brain glioma has yet to be elucidated. In this study, TUSC7 was poorly expressed in tissues and cell lines of glioma, and the lower expression was correlated with glioma of the worse histological grade. Moreover, TUSC7 is a prognostic biomarker of glioma patients. Up-regulation of TUSC7 suppressed cellular proliferation and invasion of glioma cells, and accelerated cellular apoptosis. Bioinformatics analysis showed that TUSC7 specifically binds to miR-23b. MiR-23b was up-regulated in glioma and negatively correlated with the expression of TUSC7. The miR-23b expression was inhibited remarkably by the upregulation of TUSC7 and the reciprocal inhibition was determined between TUSC7 and miR-23b.RNA pull-down and luciferase reporter assays were used to validate the sequence-specific correlation between miR-23b and TUSC7. TUSC7 inhibited the proliferation, migration and invasion of glioma cells and promoted cellular apoptosis largely bypassing miR-23b. We conclude that the lncRNA TUSC7 acted as a tumor suppressor gene negatively regulated by miR-23b, suggesting a novel therapeutic strategy against gliomas.
Insights
Tumour suppressor candidate 7 (TUSC7) acts as a tumor suppressor in glioma by inhibiting cell proliferation and invasion. This long non-coding RNA (lncRNA) is downregulated in glioma and suggests a new therapeutic strategy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The role of the novel tumor suppressor gene, Tumour suppressor candidate 7 (TUSC7), and its long non-coding RNA (lncRNA) in human brain glioma remains unclear.
- Glioma is a significant cause of cancer-related mortality, necessitating research into novel therapeutic targets and biomarkers.
Purpose of the Study:
- To investigate the expression and function of TUSC7 in human brain glioma.
- To determine the relationship between TUSC7 and miR-23b in glioma.
- To evaluate TUSC7 as a prognostic biomarker for glioma patients.
Main Methods:
- Quantitative real-time PCR to assess TUSC7 and miR-23b expression in glioma tissues and cell lines.
- Bioinformatics analysis to predict interactions between TUSC7 and microRNAs.
- Cell proliferation, apoptosis, and invasion assays to determine TUSC7 function.
- RNA pull-down and luciferase reporter assays to validate TUSC7-miR-23b interaction.
Main Results:
- TUSC7 expression was significantly lower in glioma tissues and cell lines compared to normal controls, correlating with higher histological grade.
- TUSC7 upregulation suppressed glioma cell proliferation and invasion while promoting apoptosis.
- TUSC7 directly binds to miR-23b, and miR-23b is upregulated in glioma, showing a negative correlation with TUSC7 expression.
- TUSC7 inhibited glioma cell progression largely independent of miR-23b.
Conclusions:
- TUSC7 functions as a tumor suppressor lncRNA in glioma, negatively regulated by miR-23b.
- TUSC7 serves as a potential prognostic biomarker for glioma.
- Targeting TUSC7 represents a promising novel therapeutic strategy for glioma treatment.
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