Epigenetic strategies for fetal hemoglobin induction in sickle cell disease.
TL;DR
This review discusses medicinal chemistry approaches primarily targeting HDAC1/2, LSD1, and DNMT1, with emphasis on inhibitor classes, binding mechanisms, structural features, preclinical evidence, and translational limitations, and how a better understanding of γ-globin repression may guide the development of safer and more accessible HbF-inducing agents.
Abstract
Sickle cell disease (SCD) is caused by pathogenic variants in the β-globin gene (HBB), most commonly the variant responsible for hemoglobin S, and affects an estimated 515,000 newborns each year, with the highest burden occurring in sub-Saharan Africa. Gene editing and hematopoietic stem cell transplantation have changed the therapeutic landscape, but their cost, technical complexity, and procedure-related risks still limit their wider use. For this reason, pharmacological induction of fetal hemoglobin (HbF) remains an important therapeutic strategy. HbF reduces HbS polymerization and is associated with lower disease severity, morbidity, and mortality. Among the mechanisms involved in γ-globin silencing, epigenetic regulation offers several targets that can be explored using small molecules. This review discusses medicinal chemistry approaches primarily targeting HDAC1/2, LSD1, and DNMT1, with emphasis on inhibitor classes, binding mechanisms, structural features, preclinical evidence, and translational limitations. The available data show that each target presents a distinct set of challenges. HDAC-directed strategies require improved isoform and cellular selectivity; LSD1 inhibitors must reconcile strong HbF induction with the risks associated with prolonged target engagement; and DNMT1 modulation is moving from DNA-incorporating nucleoside analogs toward reversible non-nucleoside inhibitors. We also discuss emerging approaches, including multi-target epigenetic modulation and targeted protein degradation. Together, these strategies show how a better understanding of γ-globin repression may guide the development of safer and more accessible HbF-inducing agents.
