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Updated: Nov 29, 2025

Describing a Transcription Factor Dependent Regulation of the MicroRNA Transcriptome
Published on: June 15, 2016
Long noncoding RNA ARRDC1-AS1 is activated by STAT1 and exerts oncogenic properties by sponging miR-432-5p/PRMT5 axis
Xiao-Dong Zou1, Qian Zang2, Zhen-Zhong Zhang1
1Department of Neurology, Tongde Hospital of Zhejiang Provience, Hangzhou, 310012, Zhejiang, China.
Abstract:
Dysfunction of long noncoding RNA (lncRNA) is associated with tumorigenesis of various malignancies, including glioma. Previously, lncRNA ARRDC1 antisense RNA 1(ARRDC1-AS1) has been reported to be dysregulated in several tumors. However, the roles of ARRDC1-AS1 in glioma have not been investigated. In this study, we firstly reported that ARRDC1-AS1 expression was distinctly increased in both glioma specimens and cell lines, and high ARRDC1-AS1 expression was associated with advanced clinical progression and poor prognosis of glioma patients. Additionally, STAT1 could activate the transcription of ARRDC1-AS1. Functional studies revealed that knockdown of ARRDC1-AS1 suppressed the proliferation, migration and invasion of glioma cells. Mechanisms exploration indicated ARRDC1-AS1 served as a sponge of miR-432-5p to upregulate PRMT5 expressions. Rescue experiments indicated that knockdown of miR-432-5p reversed the inhibiting effects of ARRDC1-AS1 knockdown on glioma cells. Overall, our findings highlighted the importance of STAT1/ARRDC1-AS1/miR-432-5p/PRMT5 axis in glioma progression and offered novel strategies for glioma treatments.
Insights
Long noncoding RNA ARRDC1-AS1 is upregulated in glioma and promotes tumor growth. Inhibiting ARRDC1-AS1 may offer new therapeutic strategies for glioma patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long noncoding RNAs (lncRNAs) are implicated in cancer development.
- Dysregulation of lncRNA ARRDC1-AS1 is observed in various tumors.
- The role of ARRDC1-AS1 in glioma remains unexplored.
Purpose of the Study:
- To investigate the expression and function of ARRDC1-AS1 in glioma.
- To elucidate the underlying molecular mechanisms of ARRDC1-AS1 in glioma progression.
- To explore potential therapeutic targets for glioma.
Main Methods:
- Quantitative real-time PCR to measure ARRDC1-AS1 expression in glioma tissues and cell lines.
- Analysis of the correlation between ARRDC1-AS1 expression and clinical parameters.
- In vitro functional assays (proliferation, migration, invasion) after ARRDC1-AS1 knockdown.
- Mechanism studies involving RNA immunoprecipitation and luciferase reporter assays.
- Rescue experiments to validate the role of the identified molecular axis.
Main Results:
- ARRDC1-AS1 expression is significantly increased in glioma and correlates with advanced stage and poor prognosis.
- STAT1 transcriptionally activates ARRDC1-AS1.
- Knockdown of ARRDC1-AS1 inhibits glioma cell proliferation, migration, and invasion.
- ARRDC1-AS1 acts as a molecular sponge for miR-432-5p, leading to PRMT5 upregulation.
- miR-432-5p knockdown reverses the inhibitory effects of ARRDC1-AS1 knockdown.
Conclusions:
- The STAT1/ARRDC1-AS1/miR-432-5p/PRMT5 axis plays a crucial role in glioma progression.
- ARRDC1-AS1 is a potential oncogene and therapeutic target in glioma.
- Targeting this axis may provide novel treatment strategies for glioma.
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