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TBRG4 Knockdown Suppresses Proliferation and Growth of Human Osteosarcoma Cell Lines MG63 Through PI3K/Akt Pathway
Fei Huang1, Faxue Liao1, Guangwen Ma1
1Department of Orthopaedics, The Fourth Affiliated Hospital of Anhui Medical University, Hefei, Anhui, People's Republic of China.
Background:
The transforming growth factor β regulator 4 (TBRG4) has been proved to be involved in various types of tumor. However, its contribution in human osteosarcoma (OS) is still unclear.
Patients And Methods:
In the present study, immunohistochemistry and quantitative real-time PCR were performed to investigate the expression of TBRG4 in OS tissues obtained from patients and three types of cell lines. The effect of TBRG4 knockdown using lentivirus on tumorigenesis was detected by CCK8, high-content screening analysis, colony formation assay and flow cytometric analysis. Bioinformatics analysis was operated to investigate related signaling pathways following TBRG4 knockdown.
Results:
The results showed that the expression of TBRG4 increased significantly in OS tissues and MG63 cell line. TBRG4 knockdown inhibited cell proliferation, colony and tumor formation, while activating cell apoptosis. Ingenuity Pathway Analysis and Western blot assay further indicated that TBRG4 knockdown may regulate the proliferation of human MG63 cells through PI3K/Akt signaling pathway.
Conclusion:
Our results suggest that TBRG4 may become a promising therapeutic target for the treatment of human OS.
Insights
Transforming growth factor β regulator 4 (TBRG4) is upregulated in osteosarcoma (OS). Inhibiting TBRG4 suppresses OS cell growth and promotes apoptosis, suggesting TBRG4 as a potential therapeutic target for OS.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Transforming growth factor β regulator 4 (TBRG4) is implicated in various cancers.
- The role of TBRG4 in human osteosarcoma (OS) remains largely unknown.
Purpose of the Study:
- To investigate the expression and function of TBRG4 in human osteosarcoma.
- To explore TBRG4 as a potential therapeutic target for osteosarcoma.
Main Methods:
- Immunohistochemistry and quantitative real-time PCR to assess TBRG4 expression in OS tissues and cell lines.
- TBRG4 knockdown using lentivirus to evaluate its effects on cell proliferation, colony formation, and apoptosis.
- Bioinformatics analysis and Western blot to identify associated signaling pathways.
Main Results:
- TBRG4 expression was significantly elevated in OS tissues and the MG63 cell line.
- TBRG4 knockdown inhibited cell proliferation, colony formation, and tumor growth.
- TBRG4 knockdown promoted apoptosis and was found to regulate the PI3K/Akt signaling pathway.
Conclusions:
- TBRG4 plays a crucial role in osteosarcoma progression.
- TBRG4 represents a promising therapeutic target for human osteosarcoma treatment.
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