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The Oncolytic Adenovirus VCN-01 as Therapeutic Approach Against Pediatric Osteosarcoma.
Martínez-Vélez, Naiara; Xipell, Enric; Vera, Beatriz; Acanda de la Rocha, Arlet; Zalacain, Marta; Marrodán, Lucía; Gonzalez-Huarriz, Marisol; Toledo, Gemma; Cascallo, Manel; Alemany, Ramón; Patiño, Ana; Alonso, Marta M.
Afiliación
  • Martínez-Vélez N; The Health Research Institute of Navarra (IDISNA), Pamplona, Spain. Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain. Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
  • Xipell E; The Health Research Institute of Navarra (IDISNA), Pamplona, Spain. Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain. Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
  • Vera B; The Health Research Institute of Navarra (IDISNA), Pamplona, Spain. Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain. Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
  • Acanda de la Rocha A; The Health Research Institute of Navarra (IDISNA), Pamplona, Spain. Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain. Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
  • Zalacain M; The Health Research Institute of Navarra (IDISNA), Pamplona, Spain. Department of Pediatrics, University Hospital of Navarra, Pamplona, Spain.
  • Marrodán L; The Health Research Institute of Navarra (IDISNA), Pamplona, Spain. Department of Pediatrics, University Hospital of Navarra, Pamplona, Spain.
  • Gonzalez-Huarriz M; The Health Research Institute of Navarra (IDISNA), Pamplona, Spain. Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain. Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain.
  • Toledo G; Department of Pathology, MD Anderson Cancer Center, Madrid, Spain.
  • Cascallo M; VCN Biosciences, Sant Cugat del Vallés, Barcelona, Spain.
  • Alemany R; Translational Research Laboratory, IDIBELL-Institut Catalá d'Oncologia, L'Hospitalet de Llobregat, Barcelona, Spain.
  • Patiño A; The Health Research Institute of Navarra (IDISNA), Pamplona, Spain. Department of Pediatrics, University Hospital of Navarra, Pamplona, Spain.
  • Alonso MM; The Health Research Institute of Navarra (IDISNA), Pamplona, Spain. Program in Solid Tumors and Biomarkers, Foundation for the Applied Medical Research, Pamplona, Spain. Department of Medical Oncology, University Hospital of Navarra, Pamplona, Spain. mmalonso@unav.es.
Clin Cancer Res ; 22(9): 2217-25, 2016 05 01.
Article en En | MEDLINE | ID: mdl-26603261
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Óseas / Osteosarcoma / Adenoviridae / Virus Oncolíticos Límite: Animals / Female / Humans Idioma: En Revista: Clin Cancer Res Asunto de la revista: NEOPLASIAS Año: 2016 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Óseas / Osteosarcoma / Adenoviridae / Virus Oncolíticos Límite: Animals / Female / Humans Idioma: En Revista: Clin Cancer Res Asunto de la revista: NEOPLASIAS Año: 2016 Tipo del documento: Article País de afiliación: España
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