Article ; Online: Generation of Orthotopic and Subcutaneous Patient-Derived Xenograft Models from Diverse Clinical Tissue Samples of Pediatric Extracranial Solid Tumors.
Methods in molecular biology (Clifton, N.J.)
2024 Volume 2806, Page(s) 55–74
Abstract: Realistic and renewable laboratory models that accurately reflect the distinct clinical features of childhood cancers have enormous potential to speed research progress. These models help us to understand disease biology, develop new research methods, ... ...
Abstract | Realistic and renewable laboratory models that accurately reflect the distinct clinical features of childhood cancers have enormous potential to speed research progress. These models help us to understand disease biology, develop new research methods, advance new therapies to clinical trial, and implement personalized medicine. This chapter describes methods to generate patient-derived xenograft models of neuroblastoma and rhabdomyosarcoma, two tumor types for which children with high-risk disease have abysmal survival outcomes and survivors have lifelong-debilitating effects from treatment. Further, this protocol addresses model development from diverse clinical tumor tissue samples, subcutaneous and orthotopic engraftment, and approaches to avoid model loss. |
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MeSH term(s) | Humans ; Animals ; Mice ; Neuroblastoma/pathology ; Neuroblastoma/genetics ; Rhabdomyosarcoma/pathology ; Xenograft Model Antitumor Assays/methods ; Child ; Disease Models, Animal ; Heterografts ; Precision Medicine/methods ; Cell Line, Tumor |
Language | English |
Publishing date | 2024-04-27 |
Publishing country | United States |
Document type | Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural |
ISSN | 1940-6029 |
ISSN (online) | 1940-6029 |
DOI | 10.1007/978-1-0716-3858-3_6 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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