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Updated: Jun 23, 2026

Subcellular Fractionation of Primary Chronic Lymphocytic Leukemia Cells to Monitor Nuclear/Cytoplasmic Protein Trafficking
Published on: October 23, 2019
High FOXO3a expression is associated with a poorer prognosis in AML with normal cytogenetics
Carlos M Santamaría1, Maria C Chillón, Ramón García-Sanz
1Hospital Universitario, Salamanca, Spain; Centro de Investigación Del Cáncer-IBMCC (USAL-CSIC) of Salamanca, Spain. cmsantamaria@usal.es
Abstract:
The PI3/AKT pathway is up-regulated in acute myeloid leukemia (AML), but its prognostic relevance in cytogenetically normal AML (CN-AML) is unclear. We evaluated RNA levels of AKT and two downstream substrates (FOXO3a-p27) in 110 de novo CN-AML, included in the Spanish PETHEMA therapeutic protocols. Patients with high FOXO3a gene expression displayed shorter OS (p=0.015) and RFS (p=0.048) than low FOXO3a expressers. Features selected in the multivariate analysis as having an independent prognostic value for a shorter survival were WBC>50x10(9)/L, age >65 years and high FOXO3a expression. We concluded that FOXO3a assessment could contribute to improve the molecular-based risk stratification in CN-AML.

