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IKZF1 gene deletions drive resistance to cytarabine in B-cell precursor acute lymphoblastic leukemia

Title: IKZF1 gene deletions drive resistance to cytarabine in B-cell precursor acute lymphoblastic leukemia
Authors: Vervoort,Britt M.T.; Butler,Miriam; Grünewald,Kari J.T.; van Ingen Schenau,Dorette S.; Tee,Trisha M.; Lucas,Luc; Huitema, Alwin D.R.; Boer, Judith M.; Bornhauser,Beat C.; Bourquin,Jean Pierre; Hoogerbrugge, Peter M.; van der Velden,Vincent H.J.; Kuiper, Roland P.; van der Meer,Laurens T.; van Leeuwen,Frank N.; Apotheek O&O&O; Cancer; MS Radiologie; Genetica
Publication Year: 2024
Subject Terms: Hematology
Description: IKZF1 deletions occur in 10-15% of patients with B-cell precursor acute lymphoblastic leukemia (BCP-ALL) and predict a poor outcome. However, the impact of IKZF1 loss on sensitivity to drugs used in contemporary treatment protocols has remained underexplored. Here we show in experimental models and in patients that loss of IKZF1 promotes resistance to cytarabine (AraC), a key component of both upfront and relapsed treatment protocols. We attribute this resistance, in part, to diminished import and incorporation of AraC due to reduced expression of the solute carrier hENT1. Moreover, we found elevated mRNA expression of Evi1, a known driver of therapy resistance in myeloid malignancies. Finally, a kinase directed CRISPR/Cas9-screen identified that inhibition of either mediator kinases CDK8/19 or casein kinase 2 can restore response to AraC. We conclude that this high-risk group of patients could benefit from alternative antimetabolites, or targeted therapies that re-sensitize leukemic cells to AraC.
Document Type: article in journal/newspaper
File Description: text/plain
Language: English
ISSN: 0390-6078
Relation: https://dspace.library.uu.nl/handle/1874/459561
Availability: https://dspace.library.uu.nl/handle/1874/459561
Rights: info:eu-repo/semantics/OpenAccess
Accession Number: edsbas.AB37F963
Database: BASE