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Título

Human T-ALL Xenografts

AutorFuentes, Patricia; Toribio, María Luisa CSIC ORCID; González-García, Sara CSIC ORCID
Palabras claveT-ALL
Patient-derived xenograft (PDX)
Lentiviral transduction
Immunodeficient mice
Bone marrow aspiration
Bioluminescence imaging
Fecha de publicación2020
EditorSpringer
CitaciónLeukemia Stem Cells: 215-239 (2020)
SerieMethods in Molecular Biology
2185
ResumenIntense chemotherapy regimens of patients diagnosed with T cell acute lymphoblastic leukemia (T-ALL) have proved successful for improving patient’s overall survival, especially in children. But still T-ALL treatment remains challenging, since side effects of chemotherapeutic drugs often worsen patient’s quality of life, and relapse rates remain significant. Hence, the availability of experimental animal models capable of recapitulating the biology of human T-ALL is obligatory as a critical tool to explore novel promising therapies directed against specific targets that have been previously validated in in vitro assays. For this purpose, patient-derived xenografts (PDX) of primary human T-ALL are currently of great interest as preclinical models for novel therapeutic strategies toward transition into clinical trials. In this chapter, we describe the lab workflow to perform PDX assays, from the initial processing of patient T-ALL samples, genetic in vitro modifications of leukemic cells by lentiviral transduction, inoculation routes, monitoring for disease development, and mouse organ examination, to administration of several treatments.
Versión del editorhttps://doi.org/10.1007/978-1-0716-0810-4_13
URIhttp://hdl.handle.net/10261/343575
DOI10.1007/978-1-0716-0810-4_13
ISBN978-1-0716-0809-8
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