Assessment of Total Antioxidant Capacity, 8-Hydroxy-2'-deoxy-guanosine, the Genetic Landscape, and Their Associations in BCR::ABL-1 -Negative Chronic and Blast Phase Myeloproliferative Neoplasms.

Autor: Găman MA; Faculty of Medicine, 'Carol Davila' University of Medicine and Pharmacy, 010221 Bucharest, Romania.; Department of Hematology, Centre of Hematology and Bone Marrow Transplantation, Fundeni Clinical Institute, 022328 Bucharest, Romania.; Department of Cellular and Molecular Pathology, Stefan S. Nicolau Institute of Virology, Romanian Academy, 030304 Bucharest, Romania., Mambet C; Faculty of Medicine, 'Carol Davila' University of Medicine and Pharmacy, 010221 Bucharest, Romania.; Department of Cellular and Molecular Pathology, Stefan S. Nicolau Institute of Virology, Romanian Academy, 030304 Bucharest, Romania., Neagu AI; Department of Cellular and Molecular Pathology, Stefan S. Nicolau Institute of Virology, Romanian Academy, 030304 Bucharest, Romania., Bleotu C; Department of Cellular and Molecular Pathology, Stefan S. Nicolau Institute of Virology, Romanian Academy, 030304 Bucharest, Romania., Gurban P; Department of Cellular and Molecular Pathology, Stefan S. Nicolau Institute of Virology, Romanian Academy, 030304 Bucharest, Romania., Necula L; Department of Cellular and Molecular Pathology, Stefan S. Nicolau Institute of Virology, Romanian Academy, 030304 Bucharest, Romania., Botezatu A; Department of Cellular and Molecular Pathology, Stefan S. Nicolau Institute of Virology, Romanian Academy, 030304 Bucharest, Romania., Ataman M; Department of Cellular and Molecular Pathology, Stefan S. Nicolau Institute of Virology, Romanian Academy, 030304 Bucharest, Romania., Diaconu CC; Faculty of Medicine, 'Carol Davila' University of Medicine and Pharmacy, 010221 Bucharest, Romania., Ionescu BO; Department of Hematology, Centre of Hematology and Bone Marrow Transplantation, Fundeni Clinical Institute, 022328 Bucharest, Romania., Ghiaur AE; Department of Hematology, Centre of Hematology and Bone Marrow Transplantation, Fundeni Clinical Institute, 022328 Bucharest, Romania., Tatic A; Faculty of Medicine, 'Carol Davila' University of Medicine and Pharmacy, 010221 Bucharest, Romania.; Department of Hematology, Centre of Hematology and Bone Marrow Transplantation, Fundeni Clinical Institute, 022328 Bucharest, Romania., Coriu D; Faculty of Medicine, 'Carol Davila' University of Medicine and Pharmacy, 010221 Bucharest, Romania.; Department of Hematology, Centre of Hematology and Bone Marrow Transplantation, Fundeni Clinical Institute, 022328 Bucharest, Romania., Găman AM; Department of Pathophysiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.; Clinic of Hematology, Filantropia City Hospital, 200143 Craiova, Romania., Diaconu CC; Department of Cellular and Molecular Pathology, Stefan S. Nicolau Institute of Virology, Romanian Academy, 030304 Bucharest, Romania.
Jazyk: angličtina
Zdroj: International journal of molecular sciences [Int J Mol Sci] 2024 Jun 17; Vol. 25 (12). Date of Electronic Publication: 2024 Jun 17.
DOI: 10.3390/ijms25126652
Abstrakt: Myeloproliferative neoplasms (MPNs), namely, polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF), are clonal stem cell disorders defined by an excessive production of functionally mature and terminally differentiated myeloid cells. MPNs can transform into secondary acute myeloid leukemia (sAML/blast phase MPN) and are linked to alterations in the redox balance, i.e., elevated concentrations of reactive oxygen species and markers of oxidative stress (OS), and changes in antioxidant systems. We evaluated OS in 117 chronic phase MPNs and 21 sAML cases versus controls by measuring total antioxidant capacity (TAC) and 8-hydroxy-2'-deoxy-guanosine (8-OHdG) concentrations. TAC was higher in MPNs than controls ( p = 0.03), particularly in ET ( p = 0.04) and PMF ( p = 0.01). MPL W515L -positive MPNs had higher TAC than controls ( p = 0.002) and triple-negative MPNs ( p = 0.01). PMF patients who had treatment expressed lower TAC than therapy-free subjects ( p = 0.03). 8-OHdG concentrations were similar between controls and MPNs, controls and sAML, and MPNs and sAML. We noted associations between TAC and MPNs (OR = 1.82; p = 0.05), i.e., ET (OR = 2.36; p = 0.03) and PMF (OR = 2.11; p = 0.03), but not sAML. 8-OHdG concentrations were not associated with MPNs (OR = 1.73; p = 0.62) or sAML (OR = 1.89; p = 0.49). In conclusion, we detected redox imbalances in MPNs based on disease subtype, driver mutations, and treatment history.
Competing Interests: The authors declare no conflicts of interest.
Databáze: MEDLINE
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