Integrated drug profiling and CRISPR screening identify BCR::ABL1-independent vulnerabilities in chronic myeloid leukemia.
BCR::ABL1-independent resistance
CML
CRISPR-Cas9 screening
KCTD5
TKI
drug combination
drug repurposing
drug screening
progenitor
stem cell
Journal
Cell reports. Medicine
ISSN: 2666-3791
Titre abrégé: Cell Rep Med
Pays: United States
ID NLM: 101766894
Informations de publication
Date de publication:
10 Apr 2024
10 Apr 2024
Historique:
received:
20
09
2023
revised:
10
01
2024
accepted:
27
03
2024
medline:
24
4
2024
pubmed:
24
4
2024
entrez:
23
4
2024
Statut:
aheadofprint
Résumé
BCR::ABL1-independent pathways contribute to primary resistance to tyrosine kinase inhibitor (TKI) treatment in chronic myeloid leukemia (CML) and play a role in leukemic stem cell persistence. Here, we perform ex vivo drug screening of CML CD34
Identifiants
pubmed: 38653245
pii: S2666-3791(24)00190-3
doi: 10.1016/j.xcrm.2024.101521
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
101521Informations de copyright
Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests S.A.A. has received research funding from Incyte. S.M. has received honoraria and research funding from Novartis, Pfizer, and Bristol-Myers Squibb and honoraria from DrenBio (all not related to this study).