In vivoechographic evidence of tumoral vascularization and microenvironment interactions in metastatic orthotopic human neuroblastoma xenografts
Open Access
- 28 October 2004
- journal article
- research article
- Published by Wiley in International Journal of Cancer
- Vol. 113 (6) , 881-890
- https://doi.org/10.1002/ijc.20681
Abstract
Human neuroblastoma (NB) is the second most frequent solid tumor of childhood and represents a highly heterogeneous disease at clinical and biologic levels. Little progress has been made to improve the poor prognosis of patients with high‐stage NB. Tumor progression and metastatic dissemination still represent major obstacles to the successful treatment of advanced stage disease. In order to develop and evaluate new, targeted, therapeutic strategies, fully defined and biologically relevant in vivo models of NB are strongly needed. We have developed an orthotopic model of metastatic human NB in the nude mouse, using 2 well‐characterized NB cell lines. Tumor growth, vascular properties and metastatic patterns were investigated using a sensitive and newly developed in vivo echographic technology in addition to immunohistochemistry and PCR analyses. Results show that implantation of low numbers of NB cells directly into the adrenal gland of nude mice resulted in rapid and homogeneous tumor growth without tumor morbidity. Nude mice were shown to rapidly develop highly vascularized adrenal tumors that selectively metastasized to the liver and bone marrow. In addition, the newly formed mouse vessels in orthotopic but not in heterotopic tumors, were found to express the highly angiogenic αvβ3 integrin marker, indicating the development of a truly malignant neovasculature in orthotopic conditions only. This observation confirms the impact of the regional microenvironment on tumor biology and suggests the existence of cross‐talk with the tumor cells. In conclusion, such model faithfully reproduces the growth, vascular and metastatic patterns as observed in patients. It therefore represents a powerful and biologically relevant tool to improve our understanding of the biology of NB and to develop and assess new antiangiogenic and metastasis‐targeted therapies.Keywords
Funding Information
- Emma Muschamp Foundation
- FORCE Foundation
- ICRETT Award, International Union against Cancer
This publication has 39 references indexed in Scilit:
- High level of stabilized angiostatin mediated by adenovirus delivery does not impair the growth of human neuroblastoma xenograftsCancer Gene Therapy, 2003
- Enhanced pathological angiogenesis in mice lacking β3 integrin or β3 and β5 integrinsNature Medicine, 2002
- Transfer of the murine interleukin-12 gene in vivo by a Semliki Forest virus vector induces B16 tumor regression through inhibition of tumor blood vessel formation monitored by Doppler ultrasonographyGene Therapy, 1999
- New Hemodynamic Approach to AngiogenesisInvestigative Radiology, 1999
- A metastatic neuroblastoma model in SCID miceInternational Journal of Cancer, 1996
- A murine model for bone marrow metastasis established by an i.v. injection of C-1300 neuroblastoma in A/J miceClinical & Experimental Metastasis, 1994
- Retroperitoneal inoculation of murine neuroblastoma results in a reliable model for evaluation of the antitumor immune responseJournal of Pediatric Surgery, 1994
- Requirement of Vascular Integrin α v β 3 for AngiogenesisScience, 1994
- Importance of orthotopic implantation for human tumors as model systems: relevance to metastasis and invasionClinical & Experimental Metastasis, 1993
- Role of Microvascular Endothelial Cells in InflammationJournal of Investigative Dermatology, 1993