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Updated: Dec 3, 2025

Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
Published on: October 4, 2019
LINC00210 exerts oncogenic roles in glioma by sponging miR-328
Zhifei Wang1, Hao Wu1, Hui Yan1
1Department of Neurosurgery, Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
Abstract:
Long non-coding RNAs (lncRNAs) have been reported to serve key roles in human cancer types, including glioma. However, to the best of our knowledge, the expression and function of lncRNA LINC00210 in glioma have not previously been investigated. The present study was conducted to explore the regulatory role of LINC00210 in glioma cells. The present study demonstrated that LINC00210 was significantly upregulated in glioma tissues, and high expression of LINC00210 was significantly associated with advanced clinical stage and poor prognosis in patients with glioma. It was found that LINC00210 knockdown significantly inhibited the proliferation and migration of U251 and T98G cells. The results of luciferase reporter assays indicated that LINC00210 could directly target microRNA (miR)-328 in glioma cells, and miR-328 expression was negatively correlated with LINC00210 expression in glioma tissues. LINC00210 knockdown significantly promoted the expression of miR-328 in U251 and T98G cells. Moreover, silencing miR-328 impaired the inhibitory effects of LINC00210 knockdown on the proliferation and migration of U251 and T98G cells. Therefore, the present results suggested that LINC00210 may exert an oncogenic role in glioma via sponging miR-328.
Insights
Long non-coding RNA LINC00210 is upregulated in glioma, promoting cancer progression by sponging microRNA-328. This finding offers potential therapeutic targets for glioma treatment.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) play critical roles in human cancers, including glioma.
- The specific role of lncRNA LINC00210 in glioma remains largely unexplored.
Purpose of the Study:
- To investigate the expression and regulatory function of lncRNA LINC00210 in glioma cells.
- To elucidate the underlying molecular mechanism of LINC00210 in glioma progression.
Main Methods:
- Quantitative real-time PCR to assess LINC00210 expression in glioma tissues and cell lines.
- Cell proliferation and migration assays (e.g., U251, T98G cells) following LINC00210 knockdown.
- Luciferase reporter assays to confirm direct targeting of microRNA (miR)-328 by LINC00210.
- MiR-328 mimic transfection to assess its role in modulating LINC00210 knockdown effects.
Main Results:
- LINC00210 expression was significantly upregulated in glioma tissues compared to normal tissues.
- High LINC00210 expression correlated with advanced clinical stage and poor prognosis in glioma patients.
- LINC00210 knockdown inhibited glioma cell proliferation and migration.
- LINC00210 directly targets miR-328, with inverse correlation in glioma tissues.
- LINC00210 knockdown increased miR-328 expression, and miR-328 inhibition reversed the anti-tumor effects of LINC00210 knockdown.
Conclusions:
- LINC00210 acts as an oncogenic lncRNA in glioma.
- LINC00210 promotes glioma progression by sponging miR-328.
- LINC00210-miR-328 axis represents a potential therapeutic target for glioma.
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