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Published on: March 30, 2019
circ-RANGAP1/MicroRNA-542-3p/Myosin Regulatory Light Chain Interacting Protein Axis Modulates the Osteosarcoma Cell
Jundong Sheng1, Jin Liu1, Junwang Du2
1Department of Orthopedics, First People's Hospital of Tianshui, Tianshui, 741000 Gansu, China.
Objective:
This study is aimed at exploring the influence of circular RNA- (circRNA-) RANGAP1 targeting microRNA- (miR-) 542-3p/myosin regulatory light chain interacting protein (MYLIP) on the biological function of osteosarcoma (OS) cells.
Methods:
Tumor tissues and normal tissues were collected from OS patients and circ-RANGAP1, miR-542-3p, and MYLIP expression was tested by RT-qPCR. The correlation between the clinicopathology/prognosis of patients with OS and circ-RANGAP1 expression was observed. Human OS cell line MG-63 was screened to determine the influences of circ-RANGAP1 and miR-542-3p on OS cell progression. The targeting relation of circ-RANGAP1, miR-542-3p, and MYLIP was probed.
Results:
circ-RANGAP1 expression was elevated in tumor tissues from OS patients, which was correlated to the poor clinicopathology. circ-RANGAP1 expression was augmented in males or patients younger than 20 years old or patients with advanced OS. Higher circ-RANGAP1 expression indicated a poor prognosis in OS patients. After silencing circ-RANGAP1 or elevating miR-542-3p in MG63 cells, cell progression was limited. miR-542-3p downregulation reduced the therapeutic efficacy of silenced circ-RANGAP1. circ-RANGAP1 bound with miR-542-3p to target MYLIP.
Conclusion:
Silenced circ-RANGAP1 boosts MYLIP expression via competitive binding of miR-542-3p to facilitate OS cell progression.
Insights
Circular RNA RANGAP1 (circRNA-RANGAP1) promotes osteosarcoma progression by targeting miR-542-3p to upregulate MYLIP. Silencing circRNA-RANGAP1 inhibits tumor growth, offering a potential therapeutic strategy for osteosarcoma.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Osteosarcoma (OS) is a primary bone malignancy with a poor prognosis.
- Circular RNAs (circRNAs) play crucial roles in various cancers, including OS.
- Understanding the molecular mechanisms underlying OS progression is vital for developing effective treatments.
Purpose of the Study:
- To investigate the role of circRNA-RANGAP1 in osteosarcoma.
- To explore the regulatory network involving circRNA-RANGAP1, miR-542-3p, and MYLIP in OS cells.
- To determine the impact of this pathway on OS cell biological functions.
Main Methods:
- Expression analysis of circRNA-RANGAP1, miR-542-3p, and MYLIP in OS tissues and cell lines using RT-qPCR.
- Correlation analysis between circRNA-RANGAP1 expression and clinicopathological features/prognosis.
- Functional studies in MG-63 cells involving circRNA-RANGAP1 silencing and miR-542-3p manipulation.
- Investigation of the targeting relationship between circRNA-RANGAP1, miR-542-3p, and MYLIP.
Main Results:
- circRNA-RANGAP1 was upregulated in OS tissues and associated with poor clinicopathology and prognosis.
- Elevated circRNA-RANGAP1 expression was observed in male patients, those younger than 20, and patients with advanced OS.
- Silencing circRNA-RANGAP1 or overexpressing miR-542-3p inhibited OS cell progression.
- circRNA-RANGAP1 directly targets miR-542-3p, leading to increased MYLIP expression.
Conclusions:
- circRNA-RANGAP1 promotes osteosarcoma progression by sponging miR-542-3p and upregulating MYLIP.
- circRNA-RANGAP1 serves as a potential diagnostic biomarker and therapeutic target for osteosarcoma.
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