AUTHOR=Holtzman Noa G. , Lebowitz Michael S. , Koka Rima , Baer Maria R. , Malhotra Kanam , Shahlaee Amir , Ghanbari Hossein A. , Bentzen Søren M. , Emadi Ashkan 

TITLE=Aspartate β-Hydroxylase (ASPH) Expression in Acute Myeloid Leukemia: A Potential Novel Therapeutic Target

JOURNAL=Frontiers in Oncology

VOLUME=11

YEAR=2021

URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.783744

DOI=10.3389/fonc.2021.783744

ISSN=2234-943X

ABSTRACT=<sec><title>Background</title><p>Aspartate β-hydroxylase (ASPH) is an embryonic transmembrane protein aberrantly upregulated in cancer cells, associated with malignant transformation and, in some reports, with poor clinical prognosis.</p></sec><sec><title>Objective</title><p>To report the expression patterns of ASPH in acute myeloid leukemia (AML).</p></sec><sec><title>Methods</title><p>Cell surface expression of ASPH was measured <italic>via</italic> 8-color multiparameter flow cytometry in 41 AML patient samples (31 bone marrow, 10 blood) using fluorescein isothiocyanate (FITC)-conjugated anti-ASPH antibody, SNS-622. A mean fluorescent intensity (MFI) of 10 was used as a cutoff for ASPH surface expression positivity. Data regarding patient and disease characteristics were collected.</p></sec><sec><title>Results</title><p>ASPH surface expression was found on AML blasts in 16 samples (39%). Higher ASPH expression was seen in myeloblasts of African American patients (p=0.02), but no correlation was found between ASPH expression and other patient or disease characteristics. No association was found between ASPH status and CR rate (p=0.53), EFS (p=0.87), or OS (p=0.17).</p></sec><sec><title>Conclusions</title><p>ASPH is expressed on blasts in approximately 40% of AML cases, and may serve as a new therapeutically targetable leukemia-associated antigen.</p></sec>