Hsa_circ_0097271 Knockdown Attenuates Osteosarcoma Progression via Regulating miR-640/MCAM Pathway
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Updated: Aug 22, 2025

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
1Joint Surgery, Puren Hospital Affiliated to Wuhan University of Science and Technology, Wuhan, 430081 Hubei, China.
Background:
The dysregulation of circular RNAs (circRNAs) participates in the malignant progression of multiple cancers, including osteosarcoma (OS). However, the role of circ_0097271 in OS development remains unclear. We thus aimed at unveiling the functional role and mechanism of circ_0097271 in OS.
Methods:
The expressions of circ_0097271, miR-640, and MCAM in OS were analyzed by qPCR. Cell proliferation and migration were inspected by CCK-8 assay, colony formation assay, and Transwell assay. Circ_0097271's role in vivo was assayed by establishing animal models. The predicted binding relationship between miR-640 and circ_0097271 or MCAM was verified by dual-luciferase reporter or RIP assay.
Results:
Circ_0097271's expression was enhanced in OS samples and cells. The knockdown of circ_0097271 restrained OS cell growth and migration, and its downregulation also blocked solid tumor growth in vivo. Circ_0097271 targeted miR-640 and negatively modulated miR-640 expression. MiR-640 was poorly expressed in OS, and its depletion recovered OS cell growth and migration that were repressed by circ_0097271 knockdown. MiR-640 bound to MCAM 3'UTR and thus suppressed MCAM expression. MCAM knockdown repressed OS cell growth and migration, while additional miR-640 depletion partially abolished the anticancer effects of MCAM knockdown in OS cells.
Conclusion:
Circ_0097271 is an oncogenic driver and contributes to OS development via targeting the miR-640/MCAM pathway, which provides a potential opinion for OS treatment.
Insights
Circular RNA circ_0097271 promotes osteosarcoma (OS) development by targeting the miR-640/MCAM pathway. Downregulating circ_0097271 inhibits OS cell growth and tumor progression, offering a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are implicated in the malignant progression of various cancers, including osteosarcoma (OS).
- The specific role and mechanism of circ_0097271 in OS development have not been fully elucidated.
- Understanding circ_0097271's function is crucial for developing novel therapeutic strategies for OS.
Purpose of the Study:
- To investigate the functional role of circ_0097271 in osteosarcoma (OS) development.
- To elucidate the underlying molecular mechanism of circ_0097271 in OS progression.
- To explore circ_0097271 as a potential therapeutic target for OS treatment.
Main Methods:
- Quantitative real-time PCR (qPCR) to analyze the expression of circ_0097271, miR-640, and MCAM in OS tissues and cells.
- Cellular assays (CCK-8, colony formation, Transwell) to assess the impact of circ_0097271 on OS cell proliferation and migration.
- In vivo animal models to evaluate the effect of circ_0097271 on tumor growth.
- Dual-luciferase reporter and RIP assays to confirm the binding interactions between circ_0097271, miR-640, and MCAM.
Main Results:
- Circ_0097271 expression was significantly upregulated in OS samples and cells.
- Knockdown of circ_0097271 inhibited OS cell proliferation, migration, and in vivo tumor growth.
- Circ_0097271 acted as a sponge for miR-640, leading to decreased miR-640 levels. MiR-640 targeted MCAM, suppressing its expression.
- MCAM knockdown mimicked the inhibitory effects of circ_0097271 knockdown, and miR-640 depletion partially reversed these effects.
Conclusions:
- Circ_0097271 functions as an oncogenic driver in osteosarcoma.
- The circ_0097271/miR-640/MCAM axis plays a critical role in OS development and progression.
- Circ_0097271 represents a promising therapeutic target for osteosarcoma treatment.
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