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Updated: Jul 29, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Circular non-coding RNA circ_0072088 serves as a ceRNA, targeting the miR-1225-5p/WT1 axis to regulate non-small cell
Xiaofang Zhu1, Jing Wan1, Xu You1
1Emergency Department, Jingzhou Hospital Affiliated to Yangtze University, Jingzhou, China.
Background:
Circular RNA (circRNA) circ_0072088 has been reported to be associated with NSCLC cell growth, migration, and invasion. However, the role and mechanism of circ_0072088 on NSCLC development have not yet been determined.
Methods:
Circ_0072088, microRNA-1225 (miR-1225-5p), and Wilms' tumor (WT1) suppressor gene level was detected by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Migration, invasion, and apoptosis were detected using transwell and flow cytometry assays. Matrix metallopeptidase 9 (MMP9), hexokinase 2 (HK2), and WT1 were examined using western blot assay. The biological role of circ_0072088 on NSCLC tumor growth was examined by the xenograft tumor model in vivo. Circular RNA Interactome and TargetScan were used to predict the binding between miR-1225-5p and circ_0072088 or WT1, followed by confirmation using a dual-luciferase reporter.
Results:
Circ_0072088 and WT1 were highly expressed in NSCLC tissues and cells, and miR-1225-5p was decreased. Knockdown of circ_0072088 might repress migration, invasion, and glycolysis, and facilitate apoptosis of NSCLC cells in vitro. Circ_0072088 silencing also blocked NSCLC tumor growth in vivo. Mechanistically, circ_0072088 acted as a sponge of miR-1225-5p to regulate WT1 expression.
Conclusion:
Circ_0072088 knockdown could inhibit cell growth, migration, invasion, and glycolysis partially by regulating the miR-1225-5p/WT1 axis, thus providing a promising therapeutic target for NSCLC treatment.
Insights
Circular RNA circ_0072088 promotes non-small cell lung cancer (NSCLC) progression by sponging miR-1225-5p to upregulate WT1. Silencing circ_0072088 inhibits NSCLC growth, migration, and invasion, offering a potential therapeutic strategy.
Area of Science:
- Molecular Biology
- Oncology
- Gene Regulation
Background:
- Circular RNA (circRNA) circ_0072088 is implicated in non-small cell lung cancer (NSCLC) cell proliferation, migration, and invasion.
- The precise role and underlying mechanisms of circ_0072088 in NSCLC development remain largely undetermined.
Purpose of the Study:
- To elucidate the functional role and molecular mechanism of circ_0072088 in non-small cell lung cancer (NSCLC).
- To investigate the potential of circ_0072088 as a therapeutic target for NSCLC.
Main Methods:
- Quantitative reverse transcription-polymerase chain reaction (RT-qPCR) to measure circ_0072088, microRNA-1225-5p (miR-1225-5p), and Wilms' tumor 1 (WT1) gene expression.
- Transwell and flow cytometry assays to assess cell migration, invasion, and apoptosis.
- Western blot analysis for MMP9, HK2, and WT1 protein levels.
- In vivo xenograft models and dual-luciferase reporter assays to confirm mechanism.
Main Results:
- Circ_0072088 and WT1 were upregulated, while miR-1225-5p was downregulated in NSCLC tissues and cells.
- Knockdown of circ_0072088 suppressed NSCLC cell migration, invasion, glycolysis, and promoted apoptosis in vitro.
- Circ_0072088 silencing inhibited NSCLC tumor growth in vivo.
- Mechanistically, circ_0072088 functions as a molecular sponge for miR-1225-5p, thereby regulating WT1 expression.
Conclusions:
- Circ_0072088 knockdown inhibits NSCLC cell growth, migration, invasion, and glycolysis.
- The observed effects are partially mediated through the regulation of the miR-1225-5p/WT1 axis.
- Circ_0072088 represents a promising therapeutic target for non-small cell lung cancer treatment.
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