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Updated: Feb 2, 2026

Intratibial Osteosarcoma Cell Injection to Generate Orthotopic Osteosarcoma and Lung Metastasis Mouse Models
Published on: October 28, 2021
miR-423-5p Inhibits Osteosarcoma Proliferation and Invasion Through Directly Targeting STMN1
Xuesong Wang1, Lei Peng2, Xiaojin Gong1
1Spinal Department of Qingdao Central Hospital, Qingdao Central Hospital, Qingdao, China.
Background/Aims:
Increasing evidences suggest that dysregulated expression of miRNAs contributes to the progression of various tumors. However, the underlying function of miR-423-5p in osteosarcoma remains unexplored.
Methods:
The expression of miR-423-5p and STMN1 were determined in osteosarcoma samples and cell lines via quantitative real-time PCR. Colony formation and Cell Counting Kit-8 (CCK-8) assays were performed to measure cell proliferation ability and transwell analysis was used to detect cell invasion, and dual luciferase reporter assay was perform to analysis the interaction between the miR-423-5p and STMN1.
Results:
The expression levels of miR-423-5p and STMN1 in the osteosarcoma tissues and cell lines were measured by qRT-PCR. Cell viability was determined using the clone formation and CCK-8 assays. A dual-luciferase reporter and Western blot were performed to stdudy the target gene of miR-423-5p. Here, we showed that miR-423-5p expression was downregulated in osteosarcoma tissues and cell lines. However, the expression of stathmin1 (STMN1) was downregulated in osteosarcoma tissues and cell lines. Moreover, STMN1 expression level was negatively correlated with the miR-423-5p expression in the osteosarcoma tissues. We identified STMN1 was a direct target gene of miR-423-5p in osteosarcoma cell. Overexpression of miR-423-5p inhibited osteosarcoma cell proliferation, colony formation and invasion. Furthermore, we demonstrated that STMN1 was involved in miR-423-5p-mediated cell behavior such as cell proliferation, colony formation and invasion in the osteosarcoma cell.
Conclusion:
Our present study indicated that miR-423-5p acted as a tumor suppressor gene in osteosarcoma partly through inhibiting STMN1 expression.
Insights
MicroRNA-423-5p acts as a tumor suppressor in osteosarcoma by inhibiting cell proliferation and invasion. This microRNA targets stathmin1, suggesting a novel therapeutic pathway for osteosarcoma treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Dysregulated microRNA (miRNA) expression is implicated in tumor progression.
- The specific role of miR-423-5p in osteosarcoma pathogenesis is currently unknown.
Purpose of the Study:
- To investigate the function of miR-423-5p in osteosarcoma.
- To explore the relationship between miR-423-5p and its potential target gene, stathmin1 (STMN1).
Main Methods:
- Quantitative real-time PCR (qRT-PCR) to assess miR-423-5p and STMN1 expression.
- Cell proliferation assays (colony formation, CCK-8) and invasion assays (Transwell).
- Dual-luciferase reporter assay to confirm the interaction between miR-423-5p and STMN1.
Main Results:
- miR-423-5p was downregulated in osteosarcoma tissues and cell lines.
- STMN1 expression was also downregulated and inversely correlated with miR-423-5p levels.
- Overexpression of miR-423-5p suppressed osteosarcoma cell proliferation, colony formation, and invasion, identifying STMN1 as a direct target.
Conclusions:
- miR-423-5p functions as a tumor suppressor in osteosarcoma.
- Inhibition of STMN1 expression by miR-423-5p contributes to its tumor-suppressive role.
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