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Updated: Nov 16, 2025

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
Circular RNA circ_0002137 regulated the progression of osteosarcoma through regulating miR-433-3p/ IGF1R axis
Meng Zhang1, Guang-Yang Yu1, Gang Liu1
1Department of Orthopedic, The Affiliated Huaian NO. 1 people's Hospital of Nanjing Medical University, Huaian, China.
Abstract:
Current clinical treatment targeting osteosarcoma (OS) are limited for OS patients with pulmonary metastasis or relapse, which led to high mortality (70%-85%) for advanced osteosarcoma patients. Although ongoing efforts have been made to illustrate the mechanisms of tumorigenesis and progression in OS; however, it was far for us to learn a comprehensive molecular mechanism implies in OS development. In our study, we implicated a circRNA hsa_circ_0002137, which was higher expressed in osteosarcoma tumours compared with paracancerous tissue. The dysregulated expression pattern was also found in osteosarcoma cell lines. The role of circ_0002137 was explored via down- or up-regulated experiments. It was proved that down-regulation of circ_0002137 suppressed the progress of OS, including cell invasion, cell cycle and cell apoptosis. Furthermore, the correlation between circ_0002137 and miR-433-3p was predicted using bioinformatic tools and verified utilizing RNA pull-down assay and luciferase reporter assay. Interestingly, we found that the inhibitory effect of circ_0002137 on OS was dependent of insulin-like growth factor-1 receptor (IGF1R). In conclusion, it was demonstrated that circ_0002137 could restrain the progression of OS through regulating miR-433-3p/IGF1R axis, providing a comprehensive landscape of circ_0002137 in the generation and development of OS.
Insights
Circular RNA hsa_circ_0002137 inhibits osteosarcoma progression by regulating the miR-433-3p/IGF1R axis. This finding offers a new therapeutic target for advanced osteosarcoma (OS) patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Current treatments for osteosarcoma (OS) are insufficient for patients with metastasis or relapse, leading to high mortality.
- Comprehensive molecular mechanisms underlying OS development remain largely unknown.
- Circular RNAs (circRNAs) are increasingly recognized for their roles in cancer progression.
Purpose of the Study:
- To investigate the role of circRNA hsa_circ_0002137 in osteosarcoma (OS) development and progression.
- To elucidate the molecular mechanism by which hsa_circ_0002137 influences OS.
- To identify potential therapeutic targets for advanced OS.
Main Methods:
- Expression analysis of hsa_circ_0002137 in OS tissues and cell lines.
- Functional experiments involving down-regulation and up-regulation of hsa_circ_0002137.
- Bioinformatic prediction, RNA pull-down, and luciferase reporter assays to verify interactions.
- Investigation of the regulatory axis involving hsa_circ_0002137, miR-433-3p, and insulin-like growth factor-1 receptor (IGF1R).
Main Results:
- hsa_circ_0002137 was significantly upregulated in osteosarcoma tissues and cell lines.
- Down-regulation of hsa_circ_0002137 suppressed OS cell invasion, cell cycle progression, and induced apoptosis.
- hsa_circ_0002137 was confirmed to interact with miR-433-3p and regulate IGF1R expression.
- The inhibitory effect of hsa_circ_0002137 on OS progression was dependent on the miR-433-3p/IGF1R axis.
Conclusions:
- hsa_circ_0002137 acts as a tumor promoter in osteosarcoma (OS).
- hsa_circ_0002137 restrains OS progression by regulating the miR-433-3p/IGF1R axis.
- hsa_circ_0002137 represents a potential therapeutic target for osteosarcoma.
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