| Literature DB >> 34616866 |
Arvind Singh Mer1,2, Mark D Minden1, Benjamin Haibe-Kains1,2,3,4,5, Aaron D Schimmer1,2,4.
Abstract
Acute myeloid leukemia (AML) is heterogeneous with one common subtype recognized by the presence of recurrent mutation of nucleophosmin-1 (NPM1). Emerging evidence indicates that within NPM1 mutated AML there is variation in outcome which challenges how best to characterize and treat the individual patient. Our recent findings show that there are two distinct (primitive and committed) subtypes within NPM1 mutated AML patients. These subtypes exhibit specific molecular characteristics, disease differentiation states, patient survival, and differential drug responses.Entities:
Keywords: Acute myeloid leukemia; biomarkers; machine learning; subtype; systems biology
Year: 2021 PMID: 34616866 PMCID: PMC8489904 DOI: 10.1080/23723556.2021.1924600
Source DB: PubMed Journal: Mol Cell Oncol ISSN: 2372-3556