Myelofibrosis (MF) is the Philadelphia-negative myeloproliferative neoplasm characterized by the worst prognosis and no response to conventional therapy. Driver mutations in JAK2 and CALR impact on JAK-STAT pathway activation but also on the production of reactive oxygen species (ROS). ROS play a pivotal role in inflammation-induced oxidative damage to cellular components including DNA, therefore leading to greater genomic instability and promoting cell transformation. In order to unveil the role of driver mutations in oxidative stress, we assessed ROS levels in CD34+ hematopoietic stem/progenitor cells of MF patients. Our results demonstrated that ROS production in CD34+ cells from CALR-mutated MF patients is far greater compared with patients harboring JAK2 mutation, and this leads to increased oxidative DNA damage. Moreover, CALR-mutant cells show less superoxide dismutase (SOD) antioxidant activity than JAK2-mutated ones. Here, we show that high plasma levels of total antioxidant capacity (TAC) correlate with detrimental clinical features, such as high levels of lactate dehydrogenase (LDH) and circulating CD34+ cells. Moreover, in JAK2-mutated patients, high plasma level of TAC is also associated with a poor overall survival (OS), and multivariate analysis demonstrated that high TAC classification is an independent prognostic factor allowing the identification of patients with inferior OS in both DIPSS lowest and highest categories. Altogether, our data suggest that a different capability to respond to oxidative stress can be one of the mechanisms underlying disease progression of myelofibrosis.

The Response to Oxidative Damage Correlates with Driver Mutations and Clinical Outcome in Patients with Myelofibrosis / Genovese, Elena; Mirabile, Margherita; Rontauroli, Sebastiano; Sartini, Stefano; Fantini, Sebastian; Tavernari, Lara; Maccaferri, Monica; Guglielmelli, Paola; Bianchi, Elisa; Parenti, Sandra; Carretta, Chiara; Mallia, Selene; Castellano, Sara; Colasante, Corrado; Balliu, Manjola; Bartalucci, Niccolò; Palmieri, Raffaele; Ottone, Tiziana; Mora, Barbara; Potenza, Leonardo; Passamonti, Francesco; Voso, Maria Teresa; Luppi, Mario; Vannucchi, Alessandro Maria; Tagliafico, Enrico; Manfredini, Rossella; On Behalf Of The Mynerva MYeloid NEoplasms Research Venture Airc, null. - In: ANTIOXIDANTS. - ISSN 2076-3921. - ELETTRONICO. - 11:(2022), pp. 1-15. [10.3390/antiox11010113]

The Response to Oxidative Damage Correlates with Driver Mutations and Clinical Outcome in Patients with Myelofibrosis

Guglielmelli, Paola
Writing – Original Draft Preparation
;
Balliu, Manjola;Bartalucci, Niccolò;Vannucchi, Alessandro Maria
Writing – Original Draft Preparation
;
2022

Abstract

Myelofibrosis (MF) is the Philadelphia-negative myeloproliferative neoplasm characterized by the worst prognosis and no response to conventional therapy. Driver mutations in JAK2 and CALR impact on JAK-STAT pathway activation but also on the production of reactive oxygen species (ROS). ROS play a pivotal role in inflammation-induced oxidative damage to cellular components including DNA, therefore leading to greater genomic instability and promoting cell transformation. In order to unveil the role of driver mutations in oxidative stress, we assessed ROS levels in CD34+ hematopoietic stem/progenitor cells of MF patients. Our results demonstrated that ROS production in CD34+ cells from CALR-mutated MF patients is far greater compared with patients harboring JAK2 mutation, and this leads to increased oxidative DNA damage. Moreover, CALR-mutant cells show less superoxide dismutase (SOD) antioxidant activity than JAK2-mutated ones. Here, we show that high plasma levels of total antioxidant capacity (TAC) correlate with detrimental clinical features, such as high levels of lactate dehydrogenase (LDH) and circulating CD34+ cells. Moreover, in JAK2-mutated patients, high plasma level of TAC is also associated with a poor overall survival (OS), and multivariate analysis demonstrated that high TAC classification is an independent prognostic factor allowing the identification of patients with inferior OS in both DIPSS lowest and highest categories. Altogether, our data suggest that a different capability to respond to oxidative stress can be one of the mechanisms underlying disease progression of myelofibrosis.
11
1
15
Genovese, Elena; Mirabile, Margherita; Rontauroli, Sebastiano; Sartini, Stefano; Fantini, Sebastian; Tavernari, Lara; Maccaferri, Monica; Guglielmelli, Paola; Bianchi, Elisa; Parenti, Sandra; Carretta, Chiara; Mallia, Selene; Castellano, Sara; Colasante, Corrado; Balliu, Manjola; Bartalucci, Niccolò; Palmieri, Raffaele; Ottone, Tiziana; Mora, Barbara; Potenza, Leonardo; Passamonti, Francesco; Voso, Maria Teresa; Luppi, Mario; Vannucchi, Alessandro Maria; Tagliafico, Enrico; Manfredini, Rossella; On Behalf Of The Mynerva MYeloid NEoplasms Research Venture Airc, null
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2158/1286327
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