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Updated: Mar 16, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
MicroRNA-140 represses glioma growth and metastasis by directly targeting ADAM9
Xiaogang Liu1, Shanjun Wang1, Aiqin Yuan1
1Department of Neurosurgery, Yidu Central Hospital of Weifang, Weifang, Shandong 262500, P.R. China.
Abstract:
Glioma is the most frequent primary malignant tumor of the human brain. Recently, great progress has been made in the combined therapy of glioma. However, the clinical effects of these treatments and prognosis for patients with glioma remains poor. MicroRNAs (miRNAs) have been demonstrated to play important roles in the initiation and progression of various types of human cancers, also including glioma. The present study investigated the expression patterns of microRNA‑140 (miR-140) in glioma, and the roles of miR-140 in glioma cell proliferation, migration and invasion. The results showed that miR-140 was significantly downreuglated in glioma tissues and cell lines, and low expression levels of miR-140 were correlated with World Health Organization (WHO) grade and Karnofsky performance score (KPS) of glioma patients. Restoration of miR-140 obviously suppressed glioma cell proliferation, migration and invasion. In addition, a disintegrin and metalloproteinase 9 (ADAM9) was identified as a novel direct target gene of miR-140 in glioma. Furthermore, knockdown of ADAM9 simulated the tumor suppressor functions of miR-140, while overexpression of ADAM9 abrogated these suppressive effects induced by miR-140 in glioma cells. In conclusion, the present study demonstrated the expression and clinical roles of miR-140 in glioma and suggested that miR-140 inhibited proliferation, migration and invasion of glioma cells, partially at least via suppressing ADAM9 expression. Therefore, miR-140 may be a novel candidate target for the development of therapeutic strategies for patients with glioma.
Insights
MicroRNA-140 (miR-140) is downregulated in glioma, a common brain tumor. Restoring miR-140 inhibits glioma cell growth and spread, offering a potential new therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Glioma is the most common primary malignant brain tumor with poor patient prognosis despite treatment advances.
- MicroRNAs (miRNAs) are implicated in cancer development, including glioma.
- The role of microRNA-140 (miR-140) in glioma remains largely unexplored.
Purpose of the Study:
- To investigate the expression patterns of miR-140 in glioma.
- To elucidate the functional roles of miR-140 in glioma cell proliferation, migration, and invasion.
- To identify potential molecular targets of miR-140 in glioma.
Main Methods:
- Quantitative real-time PCR to assess miR-140 expression in glioma tissues and cell lines.
- In vitro assays to evaluate the effects of miR-140 restoration on glioma cell proliferation, migration, and invasion.
- Western blotting and luciferase reporter assays to identify and validate direct target genes of miR-140.
Main Results:
- miR-140 was significantly downregulated in glioma tissues and cell lines.
- Low miR-140 expression correlated with higher World Health Organization (WHO) grade and lower Karnofsky performance score (KPS).
- Restoration of miR-140 suppressed glioma cell proliferation, migration, and invasion by targeting ADAM9 (a disintegrin and metalloproteinase 9).
Conclusions:
- miR-140 acts as a tumor suppressor in glioma.
- miR-140 inhibits glioma cell proliferation, migration, and invasion, partly through the suppression of ADAM9.
- miR-140 represents a promising therapeutic target for glioma treatment.
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