Current status and future perspectives in targeted therapy of NPM1-mutated AML

R Ranieri, G Pianigiani, S Sciabolacci, VM Perriello… - Leukemia, 2022 - nature.com
Abstract Nucleophosmin 1 (NPM1) is a nucleus-cytoplasmic shuttling protein which is
predominantly located in the nucleolus and exerts multiple functions, including regulation of …

Biological and clinical consequences of NPM1 mutations in AML

EM Heath, SM Chan, MD Minden, T Murphy, LI Shlush… - Leukemia, 2017 - nature.com
Acute myeloid leukemia (AML) is characterized by accumulation of myeloid cells in the bone
marrow because of impaired differentiation and proliferation, resulting in hematopoietic …

Acute myeloid leukemia with mutated nucleophosmin (NPM1): is it a distinct entity?

B Falini, MP Martelli, N Bolli… - Blood, The Journal …, 2011 - ashpublications.org
After the discovery of NPM1-mutated acute myeloid leukemia (AML) in 2005 and its
subsequent inclusion as a provisional entity in the 2008 World Health Organization …

Altered nucleophosmin transport in acute myeloid leukaemia with mutated NPM1: molecular basis and clinical implications

B Falini, N Bolli, A Liso, MP Martelli, R Mannucci… - Leukemia, 2009 - nature.com
Nucleophosmin (NPM1) is a highly conserved nucleo-cytoplasmic shuttling protein that
shows a restricted nucleolar localization. Mutations of NPM1 gene leading to aberrant …

Nucleophosmin (NPM1) mutations in adult and childhood acute myeloid leukaemia: towards definition of a new leukaemia entity

R Rau, P Brown - Hematological oncology, 2009 - Wiley Online Library
Nucleophosmin (NPM) is a ubiquitously expressed chaperone protein that shuttles rapidly
between the nucleus and cytoplasm, but predominantly resides in the nucleolus. It plays key …

AML with mutated NPM1 carrying a normal or aberrant karyotype show overlapping biologic, pathologic, immunophenotypic, and prognostic features

C Haferlach, C Mecucci, S Schnittger… - Blood, The Journal …, 2009 - ashpublications.org
Acute myeloid leukemia (AML) with mutated NPM1 usually carries normal karyotype (NK),
but it may harbor chromosomal aberrations whose significance remains unclear. We …

Mutational landscape of AML with normal cytogenetics: biological and clinical implications

MP Martelli, P Sportoletti, E Tiacci, MF Martelli, B Falini - Blood reviews, 2013 - Elsevier
Acute myeloid leukemia (AML) is a molecularly heterogeneous disease. Based on
cytogenetics and FISH, AML patients are stratified into three major risk categories …

NPM1‐mutated acute myeloid leukemia: New pathogenetic and therapeutic insights and open questions

B Falini - American journal of hematology, 2023 - Wiley Online Library
The nucleophosmin (NPM1) gene encodes for a multifunctional chaperone protein that is
localized in the nucleolus but continuously shuttles between the nucleus and cytoplasm …

Multilineage dysplasia has no impact on biologic, clinicopathologic, and prognostic features of AML with mutated nucleophosmin (NPM1)

B Falini, K Macijewski, T Weiss… - Blood, The Journal …, 2010 - ashpublications.org
NPM1-mutated acute myeloid leukemia (AML) is a provisional entity in the 2008 World
Health Organization (WHO) classification of myeloid neoplasms. The significance of …

Diagnostic and therapeutic pitfalls in NPM1-mutated AML: notes from the field

B Falini, S Sciabolacci, L Falini, L Brunetti, MP Martelli - Leukemia, 2021 - nature.com
Mutations of Nucleophosmin (NPM1) are the most common genetic abnormalities in adult
acute myeloid leukaemia (AML), accounting for about 30% of cases. NPM1-mutated AML …