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Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
Published on: October 4, 2019
MiR-330-3p functions as a tumor suppressor that regulates glioma cell proliferation and migration by targeting CELF1
Hongbin Wang1, Guijing Liu2, Tao Li1
1Department of Neurosurgery, Affiliated Hospital of Hebei University of Engineering, Handan, Hebei, China.
Introduction:
Glioma is a common type of neoplasm that occurs in the central nervous system. miRNAs have been demonstrated to act as critical regulators of carcinogenesis and tumor progression in multiple cancers, but the molecular mechanism of miR-330-3p in glioma remained unclear. The purpose of the study was to explore the role of miR-330-3p in glioma cell reproduction and migration.
Material And Methods:
The expression levels of miR-330-3p and CELF1 in 27 glioma tissue specimens and human glioma cell lines were examined by qRT-PCR and western blot. The TargetScan database was used to predict the relationship between miR-330-3p and CELF1. Then the target relationship was verified using dual-luciferase reporter assay. The effects of miR-330-3p/CELF1 on glioma cell proliferation were evaluated by MTT and colony formation assay. Wound healing assay was employed to measure the migration ability of glioma cells.
Results:
MiR-330-3p was found lowly expressed in glioma tissues and cells compared with adjacent tissues and normal astrocytes, while CELF1 expression was relatively high in the glioma tissues and cells. Dual-luciferase reporter assay confirmed that miR-330-3p could directly target CELF1. Furthermore, miR-330-3p could down-regulate the expression of CELF1, therefore suppressing glioma cell reproduction and migration.
Conclusions:
MiR-330-3p inhibited the propagation and migration of glioma cells by repressing CELF1 expression.
Insights
MicroRNA-330-3p (miR-330-3p) suppresses glioma cell growth and migration. This study found miR-330-3p targets and downregulates CELF1, offering a potential therapeutic target for glioma.
Area of Science:
- Neuro-oncology
- Molecular biology
- Cancer research
Background:
- Glioma is a prevalent central nervous system neoplasm.
- MicroRNAs (miRNAs) are key regulators in cancer development.
- The specific role of miR-330-3p in glioma was previously undetermined.
Purpose of the Study:
- To investigate the function of miR-330-3p in glioma cell proliferation and migration.
- To elucidate the molecular mechanism of miR-330-3p in glioma.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) and Western blot to assess expression levels.
- Dual-luciferase reporter assay to confirm direct targeting.
- MTT, colony formation, and wound healing assays to evaluate cellular effects.
Main Results:
- miR-330-3p expression was significantly lower in glioma tissues and cells compared to normal tissues.
- CELF1 expression was inversely correlated with miR-330-3p levels.
- miR-330-3p directly targets CELF1 and suppresses glioma cell proliferation and migration.
Conclusions:
- miR-330-3p acts as a tumor suppressor in glioma.
- Inhibition of glioma cell propagation and migration by miR-330-3p is mediated through CELF1 repression.
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