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A Syngeneic Orthotopic Osteosarcoma Sprague Dawley Rat Model with Amputation to Control Metastasis Rate
Published on: May 3, 2021
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EMMPRIN expression is associated with metastatic progression in osteosarcoma.
Han-Soo Kim1,2, Ha Jeong Kim1, Mi Ra Lee1
1Department of Orthopaedic Surgery, Seoul National University Hospital, 101 Daehak-ro Jongno-gu, Seoul, 03080, South Korea.
BMC Cancer
|September 27, 2021
Summary
Extracellular matrix metalloproteinase inducer (EMMPRIN) promotes osteosarcoma metastasis by increasing MMP and VEGF. Targeting EMMPRIN may offer a new therapeutic strategy for osteosarcoma patients.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Extracellular matrix metalloproteinase inducer (EMMPRIN) is a cell-surface glycoprotein overexpressed in various cancers.
- EMMPRIN drives a metastatic phenotype by stimulating matrix metalloproteinase (MMP) and vascular endothelial growth factor (VEGF) production.
- Its role in osteosarcoma, a primary bone cancer, requires further investigation.
Purpose of the Study:
- To investigate the expression levels of EMMPRIN in osteosarcoma.
- To elucidate the functional role of EMMPRIN in osteosarcoma progression and metastasis.
- To assess the prognostic significance of EMMPRIN in osteosarcoma patients.
Main Methods:
- EMMPRIN mRNA expression was quantified using RT-PCR in osteosarcoma cell lines and normal osteoblasts.
- Immunohistochemistry was employed to evaluate EMMPRIN expression in patient tumor biopsies.
- siRNA-mediated knockdown of EMMPRIN and in vivo metastasis models were utilized to determine its functional role.
Main Results:
- EMMPRIN mRNA was significantly upregulated in most osteosarcoma cell lines compared to normal cells.
- High EMMPRIN expression in patient samples correlated with shorter metastasis-free survival.
- EMMPRIN knockdown reduced invasion, MMP production, VEGF expression, and lung metastasis in vivo.
Conclusions:
- EMMPRIN significantly contributes to osteosarcoma metastasis by modulating MMP and VEGF.
- EMMPRIN is a potential therapeutic target for inhibiting osteosarcoma progression and metastasis.

