| Literature DB >> 30674214 |
Xingguo Zhu1, Aluya R Oseghale2, Lopez H Nicole1, Biaoru Li1, Betty S Pace1,2,3.
Abstract
IMPACT STATEMENT: Sickle cell disease (SCD) is a group of inherited blood disorders caused by mutations in the human β-globin gene, leading to the synthesis of abnormal hemoglobin S, chronic hemolysis, and oxidative stress. Inhibition of hemoglobin S polymerization by fetal hemoglobin holds the greatest promise for treating SCD. The transcription factor NRF2, is the master regulator of the cellular oxidative stress response and activator of fetal hemoglobin expression. In animal models, various small chemical molecules activate NRF2 and ameliorate the pathophysiology of SCD. This review discusses the mechanisms of NRF2 regulation and therapeutic strategies of NRF2 activation to design the treatment options for individuals with SCD.Entities:
Keywords: KEAP1; NRF2; Sickle cell disease; fetal hemoglobin; oxidative stress
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Year: 2019 PMID: 30674214 PMCID: PMC6405823 DOI: 10.1177/1535370219825859
Source DB: PubMed Journal: Exp Biol Med (Maywood) ISSN: 1535-3699