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Updated: Jul 15, 2026

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
Expression of major vault protein gene in osteosarcoma patients
Cristiane Arruda Dalla-Torre1, Silvia Regina Caminada de Toledo, Maisa Yoshimoto
1Department of Pediatrics, Instituto de Oncologia Pediátrica, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, Brazil, and Applied Molecular Oncology, Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada.
Abstract:
Osteosarcoma (OS) is a primary malignant tumor of bone. Despite the successful use of multiple chemotherapeutic agents in the treatment of OS, more than 30% of OS tumors remain resistant to treatment. Elucidation of cellular resistance mechanisms may lead to better treatments for cancer patients. In this study, we used the low-density expression cDNA array, GEArray Q Series Human Cancer Drug Resistance and Metabolism Gene Array to screen genes related to drug resistance in 15 OS tumors. Expression patterns of the MPV gene were validated by real time PCR on 45 OS patient tumor samples and correlated with clinical and pathological data. Major vault protein (MVP) expression was present in 24 (53%) tumor samples and absent in 21 (47%). Samples from surgery showed correlation between the expression of MVP, metastatic disease at diagnosis and event free survival (EFS). The MVP gene expression correlates with metastatic disease at diagnosis after neoadjuvant chemotherapy (p=0.048), and is also associated with worse EFS (p=0.036). These findings suggest that MVP expression is involved in one of the mechanisms of drug resistance in OS and is induced by chemotherapy.
Insights
Major vault protein (MVP) expression in osteosarcoma (OS) tumors correlates with metastasis and poorer event-free survival (EFS) after chemotherapy, suggesting MVP is involved in drug resistance mechanisms.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma (OS) is a primary bone cancer with significant treatment resistance.
- Over 30% of OS tumors are resistant to current chemotherapeutic agents.
- Understanding drug resistance mechanisms is crucial for improving patient outcomes.
Purpose of the Study:
- To screen for genes involved in drug resistance in osteosarcoma.
- To investigate the role of Major Vault Protein (MVP) in OS chemoresistance.
- To correlate MVP expression with clinical and pathological features.
Main Methods:
- Utilized GEArray Q Series Human Cancer Drug Resistance and Metabolism Gene Array for gene screening.
- Validated MVP gene expression using real-time PCR on 45 OS patient tumor samples.
- Correlated MVP expression with clinical data, including metastatic status and event-free survival (EFS).
Main Results:
- MVP expression was detected in 53% of OS tumor samples.
- MVP expression correlated with metastatic disease at diagnosis after neoadjuvant chemotherapy (p=0.048).
- MVP expression was associated with worse event-free survival (EFS) (p=0.036).
Conclusions:
- MVP expression is implicated as a mechanism of drug resistance in osteosarcoma.
- Chemotherapy appears to induce MVP expression in OS.
- MVP may serve as a potential biomarker for predicting treatment response and prognosis in OS patients.
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