O-GlcNAcylation in early stages of chronic lymphocytic leukemia: Protocol development for flow cytometry

Author:

Temesfői Viktória12,Molnár Kinga1,Kaltenecker Péter3,Réger Barbara1,Szomor Árpád4,Horváth-Szalai Zoltán1,Alizadeh Hussain4,Kajtár Béla5,Kőszegi Tamás12,Miseta Attila1,Nagy Tamás1,Faust Zsuzsanna16

Affiliation:

1. Department of Laboratory Medicine, Medical School, University of Pécs, Pécs, Hungary

2. Lab-on-a-Chip Research Group, János Szentágothai Research Center, University of Pécs, Pécs, Hungary

3. Laboratory of Actin Cytoskeleton Regulation, Institute of Genetics, Biological Research Centre, Eötvös Loránd Research Network (ELKH), Szeged, Hungary

4. Division of Hematology, 1st Department of Internal Medicine, Medical School, University of Pécs, Pécs, Hungary

5. Department of Pathology, Medical School, University of Pécs, Pécs, Hungary

6. Department of Transfusion Medicine, Medical School, University of Pécs, Pécs, Hungary

Abstract

BACKGROUND: Recent studies proved that metabolic changes in malignant disorders have an impact on protein glycosylation, however, only a few attempts have been made so far to use O-GlcNAc analysis as a prognostic tool. Glucose metabolism is reported to be altered in hematological malignancies thus, we hypothesized that monitoring intracellular O-GlcNAc levels in Rai stage 0-I (Binet A) CLL patients could give deeper insights regarding subtle metabolic changes of progression which are not completely detected by the routine follow-up procedures. OBJECTIVE: In this proof of concept study we established a flow cytometric detection method for the assessment of O-GlcNAcylation as a possible prognostic marker in CLL malignancy which was supported by fluorescence microscopy. METHODS: Healthy volunteers and CLL patients were recruited for this study. Lymphocytes were isolated, fixed and permeabilised by various methods to find the optimal experimental condition for O-GlcNAc detection by flow cytometry. O-GlcNAc levels were measured and compared to lymphocyte count and various blood parameters including plasma glucose level. RESULTS: The protocol we developed includes red blood cell lysis, formalin fixation, 0.1% Tween 20 permeabilisation and employs standardized cell number per sample and unstained controls. We have found significant correlation between O-GlcNAc levels and WBC (R2= 0.8535, p< 0.0029) and lymphocyte count (R2= 0.9225, p< 0.0006) in CLL patients. Interestingly, there was no such correlation in healthy individuals (R2= 0.05664 for O-GlcNAc vs WBC and R2= 0.04379 for O-GlcNAc vs lymphocytes). CONCLUSION: Analyzing O-GlcNAc changes in malignant disorders, specifically in malignant hematologic diseases such as CLL, could be a useful tool to monitor the progression of the disease.

Publisher

IOS Press

Subject

Cancer Research,Genetics,Oncology,General Medicine

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