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Metabolic Biomarkers Affecting Cell Proliferation and Prognosis in Polycythemia Vera

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2022 Oct 14
PMID 36230834
Authors
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Abstract

Polycythemia vera (PV) is a malignant clonal hematological disease of hematopoietic stem cells characterized by the proliferation of peripheral blood cells, and JAK2 mutation is one of the main causes of PV peripheral blood cell proliferation. Abnormal cell metabolism is a new feature of malignant proliferation of tumor cells, but the role of metabolism in the pathogenesis and prognosis of PV remains unclear. We analyzed metabolic differences of peripheral blood sera between 32 PV patients and 20 healthy controls (HCs) by liquid chromatography-mass spectrometry (LC-MS) to investigate their relationship with cell proliferation and to screen for prognosis-related metabolic biomarkers. Compared to HC, 33 endogenous metabolites were significantly changed in PV and were involved in fatty acid metabolism, glucose metabolism, sphingolipid metabolism, and amino acid metabolism pathways. Among them, seven metabolites were closely associated with JAK2 mutations, 2 of which may contribute to the proliferation of peripheral blood cells in PV patients. A set of potential prognostic metabolic biomarkers containing four metabolites was identified by a receiver operating characteristic (ROC) curve according to the risk stratification of the PV patients and their combined AUC value of 0.952, with a sensitivity of 90.905% and specificity of 90.909% at the optimal cutoff point. Metabonomics is an important tool for the study of the pathogenesis of PV and the relationship between JAK2 gene mutation. Furthermore, the potential biomarkers of this study may provide a reference for the prognosis of PV.

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References
1.
Maziere C, Conte M, Maziere J . Activation of the JAK/STAT pathway by ceramide in cultured human fibroblasts. FEBS Lett. 2001; 507(2):163-8. DOI: 10.1016/s0014-5793(01)02977-5. View

2.
Li X, Jiang Y, Meisenhelder J, Yang W, Hawke D, Zheng Y . Mitochondria-Translocated PGK1 Functions as a Protein Kinase to Coordinate Glycolysis and the TCA Cycle in Tumorigenesis. Mol Cell. 2016; 61(5):705-719. PMC: 4888784. DOI: 10.1016/j.molcel.2016.02.009. View

3.
Lukey M, Katt W, Cerione R . Targeting amino acid metabolism for cancer therapy. Drug Discov Today. 2016; 22(5):796-804. PMC: 5429979. DOI: 10.1016/j.drudis.2016.12.003. View

4.
Batchuluun B, Al Rijjal D, Prentice K, Eversley J, Burdett E, Mohan H . Elevated Medium-Chain Acylcarnitines Are Associated With Gestational Diabetes Mellitus and Early Progression to Type 2 Diabetes and Induce Pancreatic β-Cell Dysfunction. Diabetes. 2018; 67(5):885-897. PMC: 5910003. DOI: 10.2337/db17-1150. View

5.
Jung J, Shin K, Lee Y, Shin J, Park E, Jeong J . Anti-inflammatory mechanism of exogenous C2 ceramide in lipopolysaccharide-stimulated microglia. Biochim Biophys Acta. 2013; 1831(6):1016-26. DOI: 10.1016/j.bbalip.2013.01.020. View