MassIVE MSV000097461

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Ferroptotic Cell Death upon BCL2 Inhibition

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Description

B-cell acute lymphoblastic leukemia (B-ALL) is a leading cause of death in childhood and outcomes in adults remain dismal. There is therefore an urgent clinical need for therapies that target the highest risk cases. Mutations in the histone acetyltransferase CREBBP confer high-risk and increased chemoresistance in ALL. Performing a targeted drug-screen in isogenic human cell lines, we identified a number of small molecules that specifically targeted CREBBP-mutated B-ALL, with the most potent the BCL2-inhibitor Venetoclax. Of note, this acted through a non-canonical mechanism resulting in ferroptotic rather than apoptotic cell death. CREBBP-mutated cell lines showed differences in cell-cycle, metabolism, lipid composition and response to oxidative stress, predisposing them to ferroptosis, which were further dysregulated upon acquisition of Venetoclax resistance. Lastly, small-molecule inhibition of CREBBP pharmacocopies CREBBP-mutation, sensitizing B-ALL cells, regardless of genotype, to Venetoclax-induced ferroptosis in-vitro and in-vivo, providing a potential novel drug combination for broader clinical translation in B-ALL. [doi:10.25345/C5VQ2SP36] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: B-cell acute lymphoblastic leukemia (B-ALL) ; lipidomics, ferroptosis ; DatasetType:Metabolomics

Contact

Principal Investigators:
(in alphabetical order) 		Albert Koulman, University of Cambridge, United Kingdom
Submitting User: akoulman
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