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Updated: Feb 22, 2026

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
Down-regulation of RPS9 Inhibits Osteosarcoma Cell Growth through Inactivation of MAPK Signaling Pathway
Dong-Dong Cheng1, Bin Zhu1, Shi-Jie Li1
1Department of Orthopedics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, 200233, China.
Abstract:
Objectives: Osteosarcoma is the most common malignant bone tumor in adolescents; however, the mechanisms involved in the pathogenesis and progression of osteosarcoma remain to be elucidated. Researchers have provided valuable insights into the tumorigenesis of Ribosomal protein S9 (RPS9) in some cancers. The purpose of this study was to elucidate the expression, functions, and mechanisms of RPS9 in human osteosarcoma. Methods: The expression of RPS9 in osteosarcoma tissues and cell lines was evaluated by qRT-PCR and western blotting. Knockdown of RPS9 induced by RNA interference (RNAi) method in three osteosarcoma cell lines (MNNG/HOS, MG63, and U2OS) was employed to analyze the effects of RPS9 on cell proliferation and cell cycle distribution. The host signaling pathways affected by RPS9 were detected using the intracellular signaling antibody array kit PathScan®. Results: The expression of RPS9 was found to be up-regulated in human osteosarcoma tissues and cell lines. Its expression was positively correlated with Enneking stage and the tumor recurrence. Down-regulation of RPS9 inhibited osteosarcoma cell proliferation, colony-forming ability, and cell cycle G1 phase in vitro. In addition, our data demonstrated that knockdown of RPS9 repressed the protein levels of phospho-SAPK/JNK and phospho-p38. Conclusion: RPS9 is up-regulated and has a pro-tumor effect in osteosarcoma through the activation of MAPK signaling pathway and thus can be used as a potential target for gene therapy.
Insights
Ribosomal protein S9 (RPS9) is elevated in osteosarcoma, promoting tumor growth and progression. Inhibiting RPS9 may offer a new therapeutic strategy for this bone cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma is a prevalent adolescent bone cancer with incompletely understood pathogenesis.
- Ribosomal protein S9 (RPS9) has been implicated in the tumorigenesis of various cancers.
Purpose of the Study:
- To investigate the expression, function, and underlying mechanisms of RPS9 in human osteosarcoma.
- To determine RPS9's role in osteosarcoma cell proliferation, cell cycle, and associated signaling pathways.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) and western blotting assessed RPS9 expression in osteosarcoma tissues and cell lines.
- RNA interference (RNAi) was used to knock down RPS9 in MNNG/HOS, MG63, and U2OS cell lines.
- Intracellular signaling antibody array identified pathways affected by RPS9 knockdown.
Main Results:
- RPS9 expression was significantly upregulated in osteosarcoma tissues and cell lines, correlating with tumor stage and recurrence.
- RPS9 knockdown inhibited osteosarcoma cell proliferation, colony formation, and induced G1 phase arrest.
- Knockdown of RPS9 reduced the protein levels of phospho-SAPK/JNK and phospho-p38, indicating MAPK pathway involvement.
Conclusions:
- RPS9 is upregulated in osteosarcoma and exhibits pro-tumor effects.
- RPS9 promotes osteosarcoma progression via activation of the MAPK signaling pathway.
- RPS9 represents a potential therapeutic target for osteosarcoma gene therapy.
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