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Updated: Dec 31, 2025

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
Circular RNA circ_001621 promotes osteosarcoma cells proliferation and migration by sponging miR-578 and regulating
Xianglu Ji1, Liping Shan2, Peng Shen1
1Department of Orthopedic Surgery, Shengjing Hospital of China Medical University, Shenyang, Liaoning, PR China.
Abstract:
Strategies targeted vascular endothelial growth factor (VEGF)-dependent osteosarcoma progression are limited although important progress has been made in illustrating the mechanisms. Here we identified circ_001621 as one of the significantly upregulated circular RNAs (circRNAs) by circRNAs microarrays. We found that patients with high circ_001621 expression had a shorter survival time. Moreover, we found several potential sponge micro RNAs (miRNA) of circ_001621 with Circular RNA Interactome database. Among the candidate sponge, we elucidated the association of circ_001621 and miR-578. In addition, we demonstrated that miR-578 targeted circ_001621 directly. Functionally, we set up the experimental system to investigate the effects of circ_001621/miR-578/VEGF interaction in vitro and in vivo. Results indicated circ_001621-promoted osteosarcoma proliferation and migration via attenuating the inhibition of cyclin-dependent kinase 4 (CDK4) and matrix metallopeptidase 9 (MMP9) by miR-578, respectively. Nude mice experiment was further performed to estimate the promotion of metastasis by circ_001621. The present study evaluated the mechanisms underlying circ_001621 enhanced osteosarcoma progression and provided novel therapeutic targets for advanced osteosarcoma.
Insights
Circular RNA circ_001621 promotes osteosarcoma progression and metastasis by sponging miR-578, leading to increased vascular endothelial growth factor (VEGF) signaling. This study identifies circ_001621 as a potential therapeutic target for osteosarcoma.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma progression is linked to vascular endothelial growth factor (VEGF).
- Understanding the regulatory mechanisms of osteosarcoma is crucial for developing targeted therapies.
- Circular RNAs (circRNAs) are emerging as key players in cancer development.
Purpose of the Study:
- To investigate the role of circ_001621 in osteosarcoma progression.
- To elucidate the interaction between circ_001621, miR-578, and VEGF in osteosarcoma.
- To identify novel therapeutic targets for advanced osteosarcoma.
Main Methods:
- CircRNA microarrays were used to identify upregulated circRNAs.
- Bioinformatic analysis (Circular RNA Interactome) predicted potential miRNA targets.
- In vitro and in vivo experiments assessed the functional impact of the circ_001621/miR-578/VEGF axis.
- Nude mice xenografts were used to evaluate metastasis.
Main Results:
- Circ_001621 was significantly upregulated in osteosarcoma and correlated with shorter survival.
- Circ_001621 directly sponges miR-578, leading to the release of its target genes, CDK4 and MMP9.
- Circ_001621 promotes osteosarcoma proliferation, migration, and metastasis in vitro and in vivo.
Conclusions:
- Circ_001621 enhances osteosarcoma progression and metastasis by inhibiting miR-578.
- The circ_001621/miR-578/VEGF pathway represents a novel therapeutic strategy for osteosarcoma.
- Circ_001621 is a potential biomarker for osteosarcoma prognosis and a therapeutic target.
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