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Updated: Sep 28, 2025

Use of Alu Element Containing Minigenes to Analyze Circular RNAs
Published on: March 10, 2020
Circular RNA circStag1 promotes bone regeneration by interacting with HuR
Gaoyang Chen1,2, Canling Long1,2, Shang Wang1,2
1Department of Spine Surgery and Institute for Orthopaedic Research, the Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen Key Laboratory of Musculoskeletal Tissue Reconstruction and Function Restoration, Shenzhen, 518020, China.
Circular RNAs (circRNAs) like circStag1 are crucial for bone health. Downregulated circStag1 in osteoporosis suggests it can promote bone regeneration via the HuR/Wnt pathway, offering new therapeutic strategies.
Area of Science:
- Biochemistry
- Molecular Biology
- Orthopedics
Background:
- Postmenopausal osteoporosis is a metabolic bone disorder increasing fracture risk.
- Circular RNAs (circRNAs) regulate bone metabolism, but their role in osteoporosis is unclear.
- Osteoporosis involves bone microarchitecture deterioration.
Purpose of the Study:
- Investigate the function of circRNAs in postmenopausal osteoporosis.
- Identify specific circRNAs involved in bone metabolism regulation.
- Explore the molecular mechanisms underlying circRNA action in osteoporosis.
Main Methods:
- Quantified circStag1 expression in osteoporotic bone marrow mesenchymal stem cells (BMSCs) and patient samples.
- Overexpressed circStag1 in BMSCs and assessed osteogenic capability.
- Investigated circStag1 interaction with Human Antigen R (HuR) and its effect on Wnt signaling.
- Utilized circStag1-loaded adeno-associated virus (circStag1-AAV) in an ovariectomized rat model.
Main Results:
- circStag1 expression was significantly downregulated in osteoporotic BMSCs and tissues.
- Overexpression of circStag1 enhanced BMSC osteogenic differentiation.
- circStag1 promoted HuR cytoplasmic translocation, activating the Wnt pathway by stabilizing Lrp5/6 and β-catenin.
- In vivo circStag1-AAV administration promoted bone formation and prevented bone loss in rats.
Conclusions:
- circStag1 is a critical regulator of bone metabolism and osteogenesis.
- circStag1 promotes bone regeneration by modulating the HuR/Wnt signaling pathway.
- circStag1 represents a potential therapeutic target for postmenopausal osteoporosis.
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