Establishment and characterization of new orthotopic and metastatic neuroblastoma models

Treatment of metastatic neuroblastoma remains a challenge in pediatric oncology. Relevant preclinical models may improve exploration of oncogenesis and new therapies. We developed new orthotopic and metastatic models derived from stage 4 neuroblastoma. Orthotopic and systemic models were established...

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Bibliographic Details
Published in:In vivo (Athens) Vol. 28; no. 4; pp. 425 - 434
Main Authors: Daudigeos-Dubus, Estelle, LE Dret, Ludivine, Rouffiac, Valérie, Bawa, Olivia, Leguerney, Ingrid, Opolon, Paule, Vassal, Gilles, Geoerger, Birgit
Format: Journal Article
Language:English
Published: Greece 01-07-2014
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Summary:Treatment of metastatic neuroblastoma remains a challenge in pediatric oncology. Relevant preclinical models may improve exploration of oncogenesis and new therapies. We developed new orthotopic and metastatic models derived from stage 4 neuroblastoma. Orthotopic and systemic models were established in BalbC Rag2(-/-)gammaC(-/-) mice following adrenal and intravenous injection of luciferase-transfected IMR-32 and IGR-N91 cells, respectively. All four models exhibited 100% tumor take rate. Metastatic spread of orthotopic IMR-32-Luc cells was observed mainly to the lung, liver and bone; that of IGR-N91-Luc cells to liver, spleen and adrenals. Interestingly, systemic IMR-32-Luc cells metastasized rather to the lung, liver and bone, and IGR-N91-Luc to liver, lung, spleen and adrenals. Feasibility of non-invasive, real-time antitumor response evaluation was validated in the systemic models. These neuroblastoma models with distinct patterns of metastatic spread represent relevant tools for exploring local and metastatic tumor cell tropism, mechanisms of spread and evaluating new cancer therapeutics.
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ISSN:1791-7549