T-cell acute lymphoblastic leukemia (T-ALL) is a hematological malignancy, characterized by frequent loss-of-function mutations in EZH2 gene. EZH2 is a histone-lysine N- methyltransferase enzyme and in mouse, its inactivation leads to the initiation and progression of T-cell leukemia. Here, we characterized the in vitro phenotypes associated with a long-term expansion of human CD34+ hematopoietic stem and progenitor cells (HSPCs) in response to CRISPR/Cas9-mediated inactivation of EZH2 alone or in combination with the constitutive expression of known T-ALL oncogenes after lentiviral transduction. It is known that early T cell leukemias with inactivating EZH2 mutations are closely associated with the upregulation of HOXA9 and LYL1 oncogenes. In our in vitro model EZH2 knockout in LYL1 or HOXA9- transduced HSPCs, expanded in vitro up to 31 days, exhibited an increased leukemia clonogenic capacity and promoted an enrichment of early progenitor T cells at the double negative 1 (DN1) development stage. Furthermore, EZH2-null LYL1 and EZH2-null HOXA9- transduced cells demonstrated high penetrance leukemia in vivo experiments. RNA-seq data from ETP-ALL-like LOUCY cells revealed that EZH2 knockout overexpressing HOXA9 or LYL1 resulted in a gene expression signature of immature T-ALL, stem/immature immunophenotypic stage, increased replication status, and enhanced dependency on the inflammation response. Lastly, RNA-seq data analysis from a large pediatric cohort of T-ALLs revealed that patients with Loss of Function (LoF) mutations in EZH2 gene shared a stem cell- associated transcriptional program and were statistically enriched for the immature HOXA cluster and ETP subtype in human T-ALL leukemia.

The functional role of EZH2 inactivation in the pathogenesis of T-cell acute lymphoblastic leukemia / Colucci, Mattia. - (2024 May 09).

The functional role of EZH2 inactivation in the pathogenesis of T-cell acute lymphoblastic leukemia

Colucci, Mattia
09/05/2024

Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is a hematological malignancy, characterized by frequent loss-of-function mutations in EZH2 gene. EZH2 is a histone-lysine N- methyltransferase enzyme and in mouse, its inactivation leads to the initiation and progression of T-cell leukemia. Here, we characterized the in vitro phenotypes associated with a long-term expansion of human CD34+ hematopoietic stem and progenitor cells (HSPCs) in response to CRISPR/Cas9-mediated inactivation of EZH2 alone or in combination with the constitutive expression of known T-ALL oncogenes after lentiviral transduction. It is known that early T cell leukemias with inactivating EZH2 mutations are closely associated with the upregulation of HOXA9 and LYL1 oncogenes. In our in vitro model EZH2 knockout in LYL1 or HOXA9- transduced HSPCs, expanded in vitro up to 31 days, exhibited an increased leukemia clonogenic capacity and promoted an enrichment of early progenitor T cells at the double negative 1 (DN1) development stage. Furthermore, EZH2-null LYL1 and EZH2-null HOXA9- transduced cells demonstrated high penetrance leukemia in vivo experiments. RNA-seq data from ETP-ALL-like LOUCY cells revealed that EZH2 knockout overexpressing HOXA9 or LYL1 resulted in a gene expression signature of immature T-ALL, stem/immature immunophenotypic stage, increased replication status, and enhanced dependency on the inflammation response. Lastly, RNA-seq data analysis from a large pediatric cohort of T-ALLs revealed that patients with Loss of Function (LoF) mutations in EZH2 gene shared a stem cell- associated transcriptional program and were statistically enriched for the immature HOXA cluster and ETP subtype in human T-ALL leukemia.
9-mag-2024
Giambra,Vincenzo
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1710180
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