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Updated: May 14, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
The RON receptor tyrosine kinase is a potential therapeutic target in Burkitt lymphoma
Xiangmin Tong1, Xuewu Zhang, Jian Fan
1Department of Hematology, First Affiliated Hospital, Zhejiang University College of Medicine, Hangzhou, China.
Background:
Aberrant expression of the RON receptor tyrosine kinase is associated with tumor progression and carcinogenesis. The aims of this study were to determine the role and functional mechanisms of RON in Burkitt lymphoma (BL) and to document its potential as a therapeutic target.
Methods:
RON expression was determined in BL cell lines by western blot analysis and examined in human lymphoma specimens by both western blotting and immunohistochemistry. The correlation between RON expression and Epstein-Barr virus (EBV) infection was investigated. Raji cells were treated with the Zt/f2 anti-RON mAb and cell viability, colony formation, apoptosis and cell cycle arrest were measured in vitro using cell proliferation assays, colony-forming assays and flow cytometry. Downregulation of RON by Zt/f2 was validated in mice bearing Raji cell xenografts.
Results:
Immunohistostaining showed a high frequency of RON (+) cells in BL tissues and RON expression strongly correlated with EBV positivity. RON downregulation significantly decreased cell proliferation and colony formation via promotion of apoptosis and cell cycle arrest in Raji cells. The in vivo study showed that RON knockdown inhibits the tumorigenic potential of Raji cells in nude mice.
Conclusions:
RON acts as an oncogene in the carcinogenesis and progression of BL and is therefore a potential target for therapeutic intervention.
Insights
The RON receptor tyrosine kinase drives Burkitt lymphoma (BL) progression and cancer development. Inhibiting RON can decrease tumor growth by promoting cell death and halting cell cycle, making it a potential therapeutic target for BL.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- Aberrant expression of the RON receptor tyrosine kinase is linked to tumor progression and carcinogenesis.
- Understanding RON's role in Burkitt lymphoma (BL) is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the role and functional mechanisms of RON in Burkitt lymphoma.
- To evaluate RON as a potential therapeutic target for BL.
Main Methods:
- Western blot and immunohistochemistry were used to assess RON expression in BL cell lines and tissues.
- Correlation between RON expression and Epstein-Barr virus (EBV) infection was examined.
- In vitro and in vivo studies using anti-RON monoclonal antibody (mAb) assessed effects on cell viability, proliferation, apoptosis, cell cycle arrest, and tumor growth.
Main Results:
- High frequency of RON expression observed in BL tissues, strongly correlating with EBV positivity.
- Downregulation of RON significantly reduced cell proliferation and colony formation by inducing apoptosis and cell cycle arrest in Raji cells.
- In vivo studies confirmed that RON knockdown inhibits the tumorigenic potential of BL cells.
Conclusions:
- RON functions as an oncogene in the carcinogenesis and progression of Burkitt lymphoma.
- RON represents a promising therapeutic target for intervention in BL.
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