| Literature DB >> 27595736 |
Anna Mies1, Olivier Hermine2, Uwe Platzbecker3,4.
Abstract
Distinct subtypes of lower risk myelodysplastic syndromes display ring sideroblasts in the bone marrow, i. e., erythroid progenitors characterized by excessive iron deposited in the mitochondria. This morphological feature is frequently associated with somatic mutations in components of the splicing machinery that constitutes the underlying molecular principle of the disease. Conventional treatment regimen with erythropoiesis-stimulating agents often fails to induce sustained erythroid improvement in these patients that harbor defects in late-stage erythroblasts downstream of erythropoietin action. In the present review, we will discuss activin receptor ligand traps as novel therapeutic strategies particularly for sideroblastic subgroups of myelodysplastic syndromes that were recently shown to alleviate anemia by specifically inhibiting aberrant TGF-β signaling and thereby promoting erythroid differentiation.Entities:
Keywords: Activin receptor ligand trap; Luspatercept; MDS; Ring sideroblasts; SF3B1; TGF-β
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Year: 2016 PMID: 27595736 DOI: 10.1007/s11899-016-0347-9
Source DB: PubMed Journal: Curr Hematol Malig Rep ISSN: 1558-8211 Impact factor: 3.952