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Updated: Oct 9, 2025

Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
Published on: October 4, 2019
CircularLRRC7 is a Potential Tumor Suppressor Associated With miR-1281 and PDXP Expression in Glioblastoma
Xue Kong1,2,3,4, Ruiting Xu4, Wei Wang3,4
1School of Medicine, Shandong University, Jinan, China.
Abstract:
Circular RNAs (circRNAs) are usually enriched in neural tissues, yet about 80% circRNAs have lower expression in gliomas relative to normal brains, highlighting the importance of circRNAs as tumor suppressors. However, the clinical impact as well as the pathways regulated by the tumor-suppressive circRNAs remain largely unknown in glioblastoma (GBM). Through bioinformatic analysis followed by experimental validation, we found that hsa_circ_0114014 (circLRRC7) was dramatically down-regulated in GBM when compared with normal brain tissues (p < 0.0001). GBM patients with a lower circLRRC7 expression had poorer progression-free survival (PFS, p < 0.05) and overall survival (OS, p < 0.05). Analyses of the predicted target miRNAs of circLRRC7 in CSCD and CRI databases, in combination with the miRNA expression data in GBMs and normal brains from GSE database, revealed miR-1281 as a potential downstream target of circLRRC7. Subsequently, the target genes of hsa-mir-1281 were predicted by TargetScan, miRDB and miRNATAR databases. Intersection analysis and correlation test indicated that PDXP was a potential target of miR-1281. In summary, circLRRC7 may be a tumor suppressor that associated with miR-1281 and PDXP expression in GBM, which may provide novel therapeutic targets for GBM treatment.
Insights
Circular RNAs (circRNAs) function as tumor suppressors in glioblastoma. Lower expression of circLRRC7 correlates with poor patient survival and suggests a novel therapeutic pathway involving miR-1281 and PDXP.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are prevalent in neural tissues.
- Many circRNAs act as tumor suppressors, with reduced expression observed in gliomas.
- The specific roles and clinical implications of tumor-suppressive circRNAs in glioblastoma (GBM) are not well understood.
Purpose of the Study:
- To investigate the role of circLRRC7 as a potential tumor suppressor in glioblastoma.
- To identify the clinical significance of circLRRC7 expression in GBM patients.
- To elucidate the molecular pathway regulated by circLRRC7 in GBM.
Main Methods:
- Bioinformatic analysis of circRNA expression in GBM and normal brain tissues.
- Experimental validation of circLRRC7 expression levels.
- Survival analysis (progression-free and overall survival) based on circLRRC7 expression.
- Prediction and validation of miRNA and mRNA targets using bioinformatic databases and correlation analysis.
Main Results:
- circLRRC7 was significantly downregulated in GBM tissues compared to normal brain tissues (p < 0.0001).
- Low circLRRC7 expression was associated with poorer progression-free survival (PFS) and overall survival (OS) in GBM patients (p < 0.05).
- miR-1281 was identified as a potential downstream target of circLRRC7, and PDXP was predicted as a target of miR-1281.
Conclusions:
- circLRRC7 exhibits tumor-suppressive properties in glioblastoma.
- The circLRRC7/miR-1281/PDXP axis represents a potential regulatory pathway in GBM.
- circLRRC7 may serve as a novel therapeutic target for glioblastoma treatment.
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