Background:- Lymphoid enhancer-binding factor 1 (LEF1) is a downstream
effector of the Wnt/β-catenin signaling pathway, which controls cell growth and
differentiation. Dysregulation of LEF1 expression may result in several disease
patterns and hematological malignancies, as the Wnt signaling plays a pivotal
role in development and cancerogenesis. Patients and methods:- We investigated
the influence of LEF1 expression in 72 adults with cytogenetically normal acute
myeloid leukemia (CN-AML) patients together with 30 healthy controls using a
Real-Time Quantitative Reverse-Transcriptase Polymerase Chain Reaction
(RTQ-PCR) to assess the possible relation, association or correlation between
LEF1 expression and CN-AML clinical and laboratory features at diagnosis and
follow up. Results:- We found that both the expression rate and expression
level of LEF-1 gene were significantly higher in AML patients than in controls
(p=˂0.001). LEF-1 high expressors had significantly lower WBCs and BM blasts
compared to LEF-1 Low expressors, the difference was statistically significant
(p=0.03, 0.02) respectively. Hepatosplenomegaly was more encountered in LEF-1
Low expressors compared to LEF-1 high expressors (p=0.05). LEF-1 high
expressors were associated with favorable treatment outcomes as they were
associated with significantly better overall survival (p=0.001), disease-free
survival ( p=0.04), and event-free survival ( p=0.008). Complete remission (CR)
were more achieved in LEF-1 high expressors than LEF-1 Low expressors; yet the
difference was not statistically significant (p=0.1). Conclusion:- Our study
has shown that LEF1 is a favorable prognostic factor in CN-AML. It could
therefore be useful to improve risk stratification and to develop better
treatment strategies and suggest the need of alternative regimens. - See moreat:
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