NOTCH1 dimeric signaling is essential for T-cell leukemogenesis and leukemia maintenance

T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive malignancy that is characterized by an expansion of T-cell progenitors and DNA mutations that lead to overactive NOTCH1 signaling in >50% of T-ALL cases. Using synthetic models of human T-ALL, we report that NOTCH1 dimeric signaling was crucial for the leukemogenesis of human hematopoietic stem/progenitor cells (HSPCs) from cord blood. We also identified a Notch dimerization-dependent gene signature, including the HES4 transcription factor, which induced a proliferative advantage in human HSPCs and in Notch dimerization-dependent, patient-derived xenografts of T-ALL. Interestingly, in human T-ALL cells, HES4 enforced the expression of the Δ133p53 isoform with the concomitant block of proapoptotic p53 target genes and the induction of BCL2L1 gene expression and antiapoptotic B-cell lymphoma extra-large protein. In addition, through an integrated experimental approach that included genetically modified cell lines, RNA/chromatin immunoprecipitation sequencing, and single-cell RNA sequencing profiles of primary T-ALL samples, we revealed cell subsets with Notch dimerization-dependent gene signatures, which indirectly correlated with proapoptotic genes and directly associated with cell markers of poor clinical outcome in primary T-ALL samples. Taken together, these findings highlight the crucial role of NOTCH1 dimeric signaling in human T-cell leukemogenesis and T-ALL maintenance, suggesting that a possible benefit can be obtained with a therapeutic strategy that target NOTCH1 dimer signaling or its downstream effectors.

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Journal
Blood
Published
2025-02-26
DOI
https://doi.org/10.1182/blood.2024027020
Primary Topic
Acute Lymphoblastic Leukemia research
Type
article
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article

NOTCH1 dimeric signaling is essential for T-cell leukemogenesis and leukemia maintenance

Michele Santodirocco, Francesco Tamiro, Mattia Colucci, Chiara Di Nunzio et al.
Blood
Acute Lymphoblastic Leukemia research
article

NOTCH1 dimeric signaling is essential for T-cell leukemogenesis and leukemia maintenance

Michele Santodirocco, Francesco Tamiro, Mattia Colucci, Chiara Di Nunzio, Costanzo Padovano, Francesca Sansico, Andrew P. Weng, Antonio Totaro, Elisabetta De Santis, Vincenzo Giambra, Serena Di Iasio, Gaja Bruno, Kashish Doshi, Eric Gu, Valentina Canistro
article en

Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive malignancy that is characterized by an expansion of T-cell progenitors and DNA mutations that lead to overactive NOTCH1 signaling in >50% of T-ALL cases. Using synthetic models of human T-ALL, we report that NOTCH1 dimeric signaling was crucial for the leukemogenesis of human hematopoietic stem/progenitor cells (HSPCs) from cord blood. We also identified a Notch dimerization-dependent gene signature, including the HES4 transcription factor, which induced a proliferative advantage in human HSPCs and in Notch dimerization-dependent, patient-derived xenografts of T-ALL. Interestingly, in human T-ALL cells, HES4 enforced the expression of the Δ133p53 isoform with the concomitant block of proapoptotic p53 target genes and the induction of BCL2L1 gene expression and antiapoptotic B-cell lymphoma extra-large protein. In addition, through an integrated experimental approach that included genetically modified cell lines, RNA/chromatin immunoprecipitation sequencing, and single-cell RNA sequencing profiles of primary T-ALL samples, we revealed cell subsets with Notch dimerization-dependent gene signatures, which indirectly correlated with proapoptotic genes and directly associated with cell markers of poor clinical outcome in primary T-ALL samples. Taken together, these findings highlight the crucial role of NOTCH1 dimeric signaling in human T-cell leukemogenesis and T-ALL maintenance, suggesting that a possible benefit can be obtained with a therapeutic strategy that target NOTCH1 dimer signaling or its downstream effectors.

BloodVol. 145(24)
BC Cancer Agency (CA), University of Miami (US), Casa Sollievo della Sofferenza (IT), Terry Fox Research Institute (CA), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Sylvester Comprehensive Cancer Center (US)
No poverty
Openalex Percentile: Top 95%
Acute Lymphoblastic Leukemia research
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