The Simultaneous Elevation of Oxidative Stress Markers and Wilms' Tumor 1 Gene during the Progression of Myelodysplastic Syndrome

Intern Med. 2016;55(24):3661-3664. doi: 10.2169/internalmedicine.55.7156. Epub 2016 Dec 15.

Abstract

Oxidative stress is closely related to iron overload in myelodysplastic syndrome (MDS) and induces DNA damage. We evaluated the oxidative stress markers derivatives of reactive oxidative metabolites (dROM) and 8-hydroxy-2'-deoxyguanosine (8-OHdG) during azacitidine treatment in an MDS patient. Simultaneous with an increase in the expression of Wilms' Tumor 1 (WT1) gene in the peripheral blood, the serum dROM level was elevated, and this increase was observed earlier than the increases in ferritin and 8-OHdG. Throughout the clinical course, dROM and 8-OHdG correlated significantly with WT1 and with ferritin, suggesting that changes in the oxidative stress marker levels reflect not only iron overload but also disease progression of MDS.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Antimetabolites, Antineoplastic / adverse effects
  • Azacitidine / adverse effects
  • Biomarkers, Tumor / blood
  • Chest Pain / etiology
  • DNA Damage
  • Deferoxamine / therapeutic use
  • Disease Progression*
  • Fatal Outcome
  • Ferritins / blood
  • Genes, Wilms Tumor*
  • Humans
  • Iron Overload / metabolism
  • Iron Overload / physiopathology
  • Male
  • Multiple Organ Failure
  • Myelodysplastic Syndromes / blood
  • Myelodysplastic Syndromes / drug therapy
  • Myelodysplastic Syndromes / genetics*
  • Myelodysplastic Syndromes / physiopathology
  • Oxidative Stress*
  • Siderophores / therapeutic use

Substances

  • Antimetabolites, Antineoplastic
  • Biomarkers, Tumor
  • Siderophores
  • Ferritins
  • Deferoxamine
  • Azacitidine