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- W4224949063 endingPage "2169" @default.
- W4224949063 startingPage "2169" @default.
- W4224949063 abstract "T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological malignancy with no well-established prognostic biomarkers. We examined the expression of protein arginine methyltransferases across hematological malignancies and discovered high levels of PRMT7 mRNA in T-ALL, particularly in the mature subtypes of T-ALL. The genetic deletion of PRMT7 by CRISPR-Cas9 reduced the colony formation of T-ALL cells and changed arginine monomethylation patterns in protein complexes associated with the RNA and DNA processing and the T-ALL pathogenesis. Among them was RUNX1, whose target gene expression was consequently deregulated. These results suggest that PRMT7 plays an active role in the pathogenesis of T-ALL." @default.
- W4224949063 created "2022-04-28" @default.
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- W4224949063 date "2022-04-26" @default.
- W4224949063 modified "2023-10-18" @default.
- W4224949063 title "Arginine Methyltransferase PRMT7 Deregulates Expression of RUNX1 Target Genes in T-Cell Acute Lymphoblastic Leukemia" @default.
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- W4224949063 doi "https://doi.org/10.3390/cancers14092169" @default.