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Updated: Jun 1, 2026

Evaluation of Substrate Ubiquitylation by E3 Ubiquitin-ligase in Mammalian Cell Lysates
Published on: May 10, 2022
An E3 ubiquitin ligase: c-Cbl: a new therapeutic target of lung cancer
Fang-Yi Lo1, Yi-Hung Carol Tan, Hung-Chi Cheng
1Department of Pharmacology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Background:
Casitas B-lineage lymphoma (Cbl) is an E3 ubiquitin ligase of many tyrosine kinase receptors. The authors previously detected c-Cbl mutation and low protein expression in non-small cell lung cancer (NSCLC). Therefore, it was hypothesized that overexpression of wild-type c-Cbl (c-Cbl WT) exhibits tumor growth inhibition.
Methods:
Wound healing and transwell assays were conducted to examine cell motility after c-Cbl WT transfection in NSCLC cell lines. The cell cycle was investigated by flow cytometry. A549 and H1299-Luc c-Cbl WT-transfected xenografts and experimental metastasis models were performed to investigate tumor growth and metastasis inhibition in vivo.
Results:
Wound healing and transwell assays demonstrated inhibition of migration in the A549 and H226br cells 4 to 24 hours after transfection. Ectopic c-Cbl WT expression was found to reduce cell proliferation at 48 hours in A549 cells. It is important to note that A549 and H1299-Luc cells with ectopic c-Cbl WT expression demonstrated inhibition of tumor growth in vivo. A549 cells overexpressing c-Cbl WT inhibited tumor metastasis in animal models.
Conclusions:
To the best of the authors' knowledge, the current study is the first to demonstrate that c-Cbl WT protein overexpression inhibits tumor metastasis and tumor growth in lung cancer xenograft models. These results provide evidence that ectopic expression of c-Cbl WT protein can be potentially applied as targeted therapy for the treatment of lung cancer.
Insights
Overexpressing wild-type Casitas B-lineage lymphoma (c-Cbl WT) protein inhibits non-small cell lung cancer (NSCLC) cell migration, proliferation, and tumor growth. This suggests c-Cbl WT as a potential targeted therapy for lung cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Casitas B-lineage lymphoma (Cbl) is an E3 ubiquitin ligase crucial for tyrosine kinase receptor regulation.
- Previous studies identified c-Cbl mutations and low expression in non-small cell lung cancer (NSCLC).
Purpose of the Study:
- To investigate the hypothesis that wild-type c-Cbl (c-Cbl WT) overexpression inhibits tumor growth in NSCLC.
- To evaluate the therapeutic potential of c-Cbl WT in lung cancer models.
Main Methods:
- Cell migration was assessed using wound healing and transwell assays post-c-Cbl WT transfection.
- Cell cycle progression was analyzed via flow cytometry.
- Tumor growth and metastasis were evaluated in vivo using NSCLC xenograft and experimental metastasis models.
Main Results:
- c-Cbl WT expression significantly inhibited NSCLC cell migration within 4–24 hours.
- Ectopic c-Cbl WT expression reduced A549 cell proliferation at 48 hours.
- In vivo studies demonstrated that c-Cbl WT overexpression suppressed tumor growth and metastasis in lung cancer models.
Conclusions:
- This study provides the first evidence that c-Cbl WT protein overexpression inhibits tumor growth and metastasis in lung cancer xenograft models.
- Ectopic expression of c-Cbl WT shows promise as a potential targeted therapy for lung cancer treatment.
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