NPM1-mutated acute myeloid leukemia: from bench to bedside

B Falini, L Brunetti, P Sportoletti… - Blood, The Journal of …, 2020 - ashpublications.org
The nucleophosmin (NPM1) gene encodes for a multifunctional protein with prominent
nucleolar localization that shuttles between nucleus and cytoplasm. NPM1 mutations …

Hematopoietic stem cells and the immune system in development and aging

D Shevyrev, V Tereshchenko, TN Berezina… - International Journal of …, 2023 - mdpi.com
Hematopoietic stem cells (HSCs) support haematopoiesis throughout life and give rise to the
whole variety of cells of the immune system. Developing in the early embryo, passing …

Data-driven modeling of core gene regulatory network underlying leukemogenesis in IDH mutant AML

A Katebi, X Chen, D Ramirez, S Li, M Lu - npj Systems Biology and …, 2024 - nature.com
Acute myeloid leukemia (AML) is characterized by uncontrolled proliferation of poorly
differentiated myeloid cells, with a heterogenous mutational landscape. Mutations in IDH1 …

Tumor-derived neomorphic mutations in ASXL1 impairs the BAP1-ASXL1-FOXK1/K2 transcription network

YK Xia, YR Zeng, ML Zhang, P Liu, F Liu… - Protein & …, 2021 - academic.oup.com
Additional sex combs-like 1 (ASXL1) interacts with BRCA1-associated protein 1 (BAP1)
deubiquitinase to oppose the polycomb repressive complex 1 (PRC1)-mediated histone …

Integrated N- and O-Glycomics of Acute Myeloid Leukemia (AML) Cell Lines

C Blöchl, D Wang, K Madunić… - Cells, 2021 - mdpi.com
Acute myeloid leukemia (AML) is characterized by a dysregulated expansion of poorly
differentiated myeloid cells. Although patients are usually treated effectively by …

Prognostic impact of FLT3‐ITD mutation on NPM1+ acute myeloid leukaemia patients and related molecular mechanisms

X Pan, Y Chang, G Ruan, F Wei, H Jiang… - British Journal of …, 2023 - Wiley Online Library
The prognosis of acute myeloid leukaemia (AML) patients carrying NPM1 mutations is
significantly worse when accompanied by FLT3‐ITD mutations. However, accurate …

Functions of the native NPM1 protein and its leukemic mutant

B Falini, D Sorcini, VM Perriello, P Sportoletti - Leukemia, 2024 - nature.com
The nucleophosmin (NPM1) gene encodes for the most abundant nucleolar protein. Thanks
to its property to act as histone chaperone and to shuttle between the nucleus and …

ARPIR: automatic RNA-Seq pipelines with interactive report

G Spinozzi, V Tini, A Adorni, B Falini, MP Martelli - BMC bioinformatics, 2020 - Springer
Background RNA-Seq is an increasing used methodology to study either coding and non-
coding RNA expression. There are many software tools available for each phase of the RNA …

Bcor deficiency perturbs erythro-megakaryopoiesis and cooperates with Dnmt3a loss in acute erythroid leukemia onset in mice

P Sportoletti, D Sorcini, AG Guzman, JM Reyes… - Leukemia, 2021 - nature.com
Recurrent loss-of-function mutations of BCL6 co-repressor (BCOR) gene are found in about
4% of AML patients with normal karyotype and are associated with DNMT3a mutations and …

Nucleophosmin 1: from its pathogenic role to a tantalizing therapeutic target in acute myeloid leukemia

Y Shi, Y Xue, C Wang, L Yu - Hematology, 2022 - Taylor & Francis
ABSTRACT Nucleophosmin 1 (NPM1, also known as B23) is a multifunctional protein
involved in a variety of cellular processes, including ribosomal maturation, centrosome …