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Cancer Therapy: Preclinical

The Oncolytic Adenovirus VCN-01 as Therapeutic Approach Against Pediatric Osteosarcoma

Naiara Martínez-Vélez, Enric Xipell, Beatriz Vera, Arlet Acanda de la Rocha, Marta Zalacain, Lucía Marrodán, Marisol Gonzalez-Huarriz, Gemma Toledo, Manel Cascallo, Ramón Alemany, Ana Patiño and Marta M. Alonso
Naiara Martínez-Vélez
1The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
2Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain.
3Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
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Enric Xipell
1The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
2Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain.
3Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
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Beatriz Vera
1The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
2Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain.
3Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
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Arlet Acanda de la Rocha
1The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
2Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain.
3Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
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Marta Zalacain
1The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
4Department of Pediatrics, University Hospital of Navarra, Pamplona, Spain.
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Lucía Marrodán
1The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
4Department of Pediatrics, University Hospital of Navarra, Pamplona, Spain.
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Marisol Gonzalez-Huarriz
1The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
2Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain.
3Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
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Gemma Toledo
5Department of Pathology, MD Anderson Cancer Center, Madrid, Spain.
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Manel Cascallo
6VCN Biosciences, Sant Cugat del Vallés, Barcelona, Spain.
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Ramón Alemany
7Translational Research Laboratory, IDIBELL-Institut Catalá d'Oncologia, L'Hospitalet de Llobregat, Barcelona, Spain.
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Ana Patiño
1The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
4Department of Pediatrics, University Hospital of Navarra, Pamplona, Spain.
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Marta M. Alonso
1The Health Research Institute of Navarra (IDISNA), Pamplona, Spain.
2Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain.
3Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
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  • For correspondence: mmalonso@unav.es
DOI: 10.1158/1078-0432.CCR-15-1899 Published May 2016
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Abstract

Purpose: Osteosarcoma is the most common malignant bone tumor in children and adolescents. Despite aggressive chemotherapy, more than 30% of patients do not respond and develop bone or lung metastasis. Oncolytic adenoviruses engineered to specifically destroy cancer cells are a feasible option for osteosarcoma treatment. VCN-01 is a replication-competent adenovirus specifically engineered to replicate in tumors with a defective RB pathway, presents an enhanced infectivity through a modified fiber and an improved distribution through the expression of a soluble hyaluronidase. The aim of this study is to elucidate whether the use of VCN-01 would be an effective therapeutic strategy for pediatric osteosarcoma.

Experimental Design: We used osteosarcoma cell lines established from patients with metastatic disease (531MII, 678R, 588M, and 595M) and a commercial cell line (143B). MTT assays were carried out to evaluate the cytotoxicity of VCN-01. Hexon assays were used to evaluate the replication of the virus. Western blot analysis was performed to assess the expression levels of viral proteins and autophagic markers. The antitumor effect of VCN-01 was evaluated in orthotopic and metastatic osteosarcoma murine animal models.

Results: This study found that VCN-01, a new generation genetically modified oncolytic adenovirus, administered locally or systemically, had a potent antisarcoma effect in vitro and in vivo in mouse models of intratibial and lung metastatic osteosarcoma. Moreover, VCN-01 administration showed a safe toxicity profile.

Conclusions: These results uncover VCN-01 as a promising strategy for osteosarcoma, setting the bases to propel a phase I/II trial for kids with this disease. Clin Cancer Res; 22(9); 2217–25. ©2015 AACR.

Footnotes

  • Note: Supplementary data for this article are available at Clinical Cancer Research Online (http://clincancerres.aacrjournals.org/).

  • Received August 7, 2015.
  • Revision received October 19, 2015.
  • Accepted November 12, 2015.
  • ©2015 American Association for Cancer Research.
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Clinical Cancer Research: 22 (9)
May 2016
Volume 22, Issue 9
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The Oncolytic Adenovirus VCN-01 as Therapeutic Approach Against Pediatric Osteosarcoma
Naiara Martínez-Vélez, Enric Xipell, Beatriz Vera, Arlet Acanda de la Rocha, Marta Zalacain, Lucía Marrodán, Marisol Gonzalez-Huarriz, Gemma Toledo, Manel Cascallo, Ramón Alemany, Ana Patiño and Marta M. Alonso
Clin Cancer Res May 1 2016 (22) (9) 2217-2225; DOI: 10.1158/1078-0432.CCR-15-1899

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The Oncolytic Adenovirus VCN-01 as Therapeutic Approach Against Pediatric Osteosarcoma
Naiara Martínez-Vélez, Enric Xipell, Beatriz Vera, Arlet Acanda de la Rocha, Marta Zalacain, Lucía Marrodán, Marisol Gonzalez-Huarriz, Gemma Toledo, Manel Cascallo, Ramón Alemany, Ana Patiño and Marta M. Alonso
Clin Cancer Res May 1 2016 (22) (9) 2217-2225; DOI: 10.1158/1078-0432.CCR-15-1899
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