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Updated: May 7, 2026

A Syngeneic Orthotopic Osteosarcoma Sprague Dawley Rat Model with Amputation to Control Metastasis Rate
Published on: May 3, 2021
Surface proteomic analysis of osteosarcoma identifies EPHA2 as receptor for targeted drug delivery
J Posthumadeboer1, S R Piersma, T V Pham
1Department of Orthopaedic Surgery, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands.
Background:
Osteosarcoma (OS) is the most common bone tumour in children and adolescents. Despite aggressive therapy regimens, treatment outcomes are unsatisfactory. Targeted delivery of drugs can provide higher effective doses at the site of the tumour, ultimately improving the efficacy of existing therapy. Identification of suitable receptors for drug targeting is an essential step in the design of targeted therapy for OS.
Methods:
We conducted a comparative analysis of the surface proteome of human OS cells and osteoblasts using cell surface biotinylation combined with nano-liquid chromatography - tandem mass spectrometry-based proteomics to identify surface proteins specifically upregulated on OS cells. This approach generated an extensive data set from which we selected a candidate to study for its suitability as receptor for targeted treatment delivery to OS. First, surface expression of the ephrin type-A receptor 2 (EPHA2) receptor was confirmed using FACS analysis. Ephrin type-A receptor 2 expression in human tumour tissue was tested using immunohistochemistry. Receptor targeting and internalisation studies were conducted to assess intracellular uptake of targeted modalities via EPHA2. Finally, tissue micro arrays containing cores of human OS tissue were stained using immunohistochemistry and EPHA2 staining was correlated to clinical outcome measures.
Results:
Using mass spectrometry, a total of 2841 proteins were identified of which 156 were surface proteins significantly upregulated on OS cells compared with human primary osteoblasts. Ephrin type-A receptor 2 was highly upregulated and the most abundant surface protein on OS cells. In addition, EPHA2 was expressed in a vast majority of human OS samples. Ephrin type-A receptor 2 effectively mediates internalisation of targeted adenoviral vectors into OS cells. Patients with EPHA2-positive tumours showed a trend toward inferior overall survival.
Conclusion:
The results presented here suggest that the EPHA2 receptor can be considered an attractive candidate receptor for targeted delivery of therapeutics to OS.
Insights
Ephrin type-A receptor 2 (EPHA2) is highly expressed on osteosarcoma (OS) cells, making it a promising target for drug delivery. This receptor facilitates targeted therapy, potentially improving treatment outcomes for this common childhood bone cancer.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Osteosarcoma (OS) is a prevalent bone tumor in children and adolescents with poor treatment outcomes.
- Targeted drug delivery offers a strategy to enhance therapeutic efficacy by concentrating drugs at the tumor site.
- Identifying specific surface receptors on OS cells is crucial for developing effective targeted therapies.
Purpose of the Study:
- To identify surface proteins upregulated on OS cells for potential therapeutic targeting.
- To evaluate the suitability of Ephrin type-A receptor 2 (EPHA2) as a target for drug delivery in OS.
Main Methods:
- Comparative proteomic analysis of OS cells and osteoblasts using mass spectrometry.
- Validation of EPHA2 surface expression via FACS and immunohistochemistry.
- Assessment of EPHA2-mediated internalization of targeted vectors and correlation with clinical outcomes.
Main Results:
- 156 surface proteins were significantly upregulated on OS cells, with EPHA2 being the most abundant.
- EPHA2 is expressed in most human OS samples and mediates targeted adenoviral vector internalization.
- A trend towards inferior overall survival was observed in patients with EPHA2-positive tumors.
Conclusions:
- Ephrin type-A receptor 2 (EPHA2) is a highly promising candidate receptor for targeted therapeutic delivery in osteosarcoma.
- Targeting EPHA2 may improve drug delivery and treatment efficacy for OS patients.
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