Characterization of CRLF2 Expression in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia

BACKGROUND: Acute lymphoblastic leukemia (ALL) is a heterogeneous disease with several underlying genetic ab-normalities. Several studies have tried to elucidate the prognostic significance of cytokine receptor-like factor 2 (CRLF2) overexpression in pediatric B-cell precursor (BCP)-ALL; however, it is still controversial.

METHODS: CRLF2 expression was assessed by flow cytometry in 87 newly diagnosed BCP-ALL pediatric patients, and 80 age and gender-matched control group. Janus Kinase2 (JAK2) (R683) mutation analysis was also performed in those identified to have CRLF2 overexpression with adequate DNA samples by direct sequencing.

RESULTS: CRLF2 overexpression was identified in 26/87 (29.9%) of our patients with cutoff set at mean fluorescence intensity (MFI = 3.8) using the Receiver Operating Characteristic (ROC) curve. There were no significant differences in the clinical and laboratory features between patients with high and low-CRLF2 expression, apart from thrombocytopenia which showed statistically significant association with the low-expression group (p = 0.041). Sequence analysis of samples with high CRLF2 expression (n = 23) revealed that 2/23 (8.7%) cases harbored the mutation JAK2 (R683). CRLF2 levels did not have a significant impact on either overall survival (OS) or disease free survival (DFS) (p = 0.601; p = 0.212, respectively).

CONCLUSIONS: CRLF2 overexpression was not an adverse parameter in pediatric BCP-ALL patients. However, patients with CRLF2 overexpression may harbor the JAK2 mutation presenting a group that can benefit from targeted therapy by kinase inhibitors. The usage of CRLF2 expression to monitor minimal residual disease of BCP-ALL would be an area of interest for further evaluation.

Medienart:

E-Artikel

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:67

Enthalten in:

Clinical laboratory - 67(2021), 1 vom: 01. Jan.

Sprache:

Englisch

Beteiligte Personen:

Rasekh, Eman O [VerfasserIn]
Atef, Asmaa M [VerfasserIn]
Khalil, Mohamed [VerfasserIn]
Ebeid, Emad [VerfasserIn]
Madney, Youssef [VerfasserIn]
Hamdy, Nayera [VerfasserIn]

Links:

Volltext

Themen:

CRLF2 protein, human
Journal Article
Receptors, Cytokine

Anmerkungen:

Date Completed 21.06.2021

Date Revised 31.05.2022

published: Print

Citation Status MEDLINE

doi:

10.7754/Clin.Lab.2020.200414

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM320535029