2025
Robust acute myeloid leukemia engraftment in humanized scaffolds using injectable biomaterials and intravenous xenotransplantation
BUŠA, Daniel; Zdeňka HERUDKOVÁ; Jan HÝL; Jakub VLAŽNÝ; Filip SOKOL et. al.Basic information
Original name
Robust acute myeloid leukemia engraftment in humanized scaffolds using injectable biomaterials and intravenous xenotransplantation
Authors
BUŠA, Daniel; Zdeňka HERUDKOVÁ; Jan HÝL; Jakub VLAŽNÝ; Filip SOKOL; Květoslava MATULOVÁ; Adam FOLTA; Jakub HYNŠT; Lucy VOJTOVA; Leoš KŘEN; Martin REPKO; Zdeněk RÁČIL; Jiří MAYER and Martin ČULEN
Edition
Molecular oncology, HOBOKEN, WILEY, 2025, 1574-7891
Other information
Language
English
Type of outcome
Article in a journal
Field of Study
30205 Hematology
Country of publisher
United States of America
Confidentiality degree
is not subject to a state or trade secret
References:
Impact factor
Impact factor: 5.000 in 2023
Organization unit
Faculty of Medicine
UT WoS
001401325000001
EID Scopus
999
Keywords in English
AML; collagen; mouse model; ossicles; patient-derived xenografts; T-cell
Tags
International impact, Reviewed
Changed: 4/2/2025 12:49, Mgr. Tereza Miškechová
Abstract
V originále
Patient-derived xenografts (PDXs) can be improved by implantation of a humanized niche. Nevertheless, the overall complexity of the current protocols, as well as the use of specific biomaterials and procedures, limits the wider adoption of this approach. Here, we identify the essential minimum steps required to create the humanized scaffolds and achieve successful acute myeloid leukemia (AML) engraftment. We compared seven biomaterials, which included both published and custom-designed materials. The highest level of bone marrow niche was achieved with extracellular matrix gels and custom collagen fiber, both of which allowed for a simple non-surgical implantation. The biomaterial selection did not influence the following AML infiltration. Regarding xenotransplantation, standard intravenous administration produced the most robust engraftment, even for two out of four otherwise non-engrafting AML samples. In contrast, direct intra-scaffold xenotransplantation did not offer any advantage. In summary, we demonstrate that the combination of an injectable biomaterial for scaffold creation plus an intravenous route for AML xenotransplantation provide the most convenient and robust approach to produce AML PDX using a humanized niche.
Links
LX22NPO5102, research and development project |
| ||
MUNI/A/1558/2023, interní kód MU |
|