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Updated: Jun 3, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
MicroRNA-10b induces glioma cell invasion by modulating MMP-14 and uPAR expression via HOXD10
Lihua Sun1, Wei Yan, Yingyi Wang
1Department of Neurosurgery, the First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, PR China.
Abstract:
MicroRNAs are small endogenous noncoding RNAs, which modulate target gene expression by binding with target mRNA sequences in the 3'untranslated region (UTR) with an imperfect complementarity that inhibits the mRNA translation. Many microRNAs have been reported to function as tumor oncogenes or anti-oncogenes. Recently, more and more microRNAs have been reported to contribute to a tumor's invasive potential. Here, we show that microRNA-10b (miR-10b) was over-expressed in glioma samples and directly associated with the glioma's pathological grade and malignancy. We also found that miR-10b induced glioma cell invasion by modulating tumor invasion factors MMP-14 and uPAR expression via the direct target HOXD10. The miR-10b/HOXD10/MMP-14/uPAR signaling pathway might contribute to the invasion of glioma. Accordingly, glioma cells lost their invasive ability when treated with specific antisense oligonucleotides (miR-10b inhibitors), suggesting that miR-10b could be used as a new bio-target to cure glioma.
Insights
MicroRNA-10b (miR-10b) promotes glioma invasion by regulating HOXD10, MMP-14, and uPAR. Inhibiting miR-10b reduced glioma cell invasion, suggesting it as a potential therapeutic target for glioma.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- MicroRNAs (miRNAs) are small noncoding RNAs regulating gene expression.
- Aberrant miRNA expression is linked to various cancers, including glioma.
- Specific miRNAs can influence tumor invasion and malignancy.
Purpose of the Study:
- To investigate the role of microRNA-10b (miR-10b) in glioma.
- To elucidate the molecular mechanisms underlying miR-10b-mediated glioma invasion.
- To evaluate miR-10b as a potential therapeutic target for glioma.
Main Methods:
- Analysis of miR-10b expression in glioma samples.
- Investigating the correlation between miR-10b levels and glioma pathological grade.
- Luciferase reporter assays and Western blotting to confirm target interactions.
- In vitro cell invasion assays using miR-10b inhibitors.
Main Results:
- miR-10b was significantly over-expressed in glioma tissues and correlated with higher pathological grades.
- miR-10b directly targets HOXD10, leading to increased expression of invasion factors MMP-14 and uPAR.
- Inhibition of miR-10b using antisense oligonucleotides reduced glioma cell invasion.
- The miR-10b/HOXD10/MMP-14/uPAR pathway was identified as crucial for glioma invasion.
Conclusions:
- miR-10b plays a critical role in promoting glioma cell invasion and malignancy.
- The miR-10b/HOXD10/MMP-14/uPAR pathway is a key regulator of glioma invasion.
- Targeting miR-10b represents a promising therapeutic strategy for glioma treatment.
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