Skip to Main content Skip to Navigation
Journal articles

A variant erythroferrone disrupts iron homeostasis in SF3B1-mutated myelodysplastic syndrome

Sabrina Bondu 1 Anne-Sophie Alary 1, 2 Carine Lefevre 1, 3 Alexandre Houy 4 Grace Jung 5 Thibaud Lefebvre 3, 6 David Rombaut 1 Ismael Boussaid 1 Abderrahmane Bousta 1 François Guillonneau 1, 7 Prunelle Perrier 8 Samar Alsafadi 4 Michel Wassef 9 Raphael Margueron 9 Alice Rousseau 1 Nathalie Droin 10, 11 Nicolas Cagnard 12 Sophie Kaltenbach 13 Susann Winter 14 Anne-Sophie Kubasch 15 Didier Bouscary 2, 1 Valeria Santini 16 Andrea Toma 17 Mathilde Hunault 18 Aspasia Stamatoullas 19 Emmanuel Gyan 20 Thomas Cluzeau 21 Uwe Platzbecker 15 Lionel Ades 22 Hervé Puy 3, 6 Marc-Henri Stern 23 Zoubida Karim 3, 6 Patrick Mayeux 1, 3, 7 Elizabeta Nemeth 5 Sophie Park 24 Tomas Ganz 5 Léon Kautz 8 Olivier Kosmider 1, 3, 2 Michaela Fontenay 1, 3, 2
7 3P5 - Plateforme protéomique 3P5 [Institut Cochin]
IC UM3 (UMR 8104 / U1016) - Institut Cochin
20 LNOx - ERL 7001 LNOx (Leukemic Niche & redOx metabolism / Niche leucémique et métabolisme redOx)
CHRU Tours - Centre Hospitalier Régional Universitaire de Tours, CNRS - Centre National de la Recherche Scientifique : EMR7001 / ERL7001, GICC EA 7501 - Groupe innovation et ciblage cellulaire (GICC), EA 7501 [2018-...]
Abstract : Myelodysplastic syndromes (MDS) with ring sideroblasts are hematopoietic stem cell disorders with erythroid dysplasia and mutations in the SF3B1 splicing factor gene. Patients with MDS with SF3B1 mutations often accumulate excessive tissue iron, even in the absence of transfusions, but the mechanisms that are responsible for their parenchymal iron overload are unknown. Body iron content, tissue distribution, and the supply of iron for eryth-ropoiesis are controlled by the hormone hepcidin, which is regulated by erythroblasts through secretion of the erythroid hormone erythroferrone (ERFE). Here, we identified an alternative ERFE transcript in patients with MDS with the SF3B1 mutation. Induction of this ERFE transcript in primary SF3B1-mutated bone marrow erythroblasts generated a variant protein that maintained the capacity to suppress hepcidin transcription. Plasma concentrations of ERFE were higher in patients with MDS with an SF3B1 gene mutation than in patients with SF3B1 wild-type MDS. Thus, hepcidin suppression by a variant ERFE is likely responsible for the increased iron loading in patients with SF3B1-mutated MDS, suggesting that ERFE could be targeted to prevent iron-mediated toxicity. The expression of the variant ERFE transcript that was restricted to SF3B1-mutated erythroblasts decreased in lenalidomide-responsive anemic patients, identifying variant ERFE as a specific biomarker of clonal erythropoiesis.
Complete list of metadata

Cited literature [76 references]  Display  Hide  Download
Contributor : Léon Kautz Connect in order to contact the contributor
Submitted on : Wednesday, January 22, 2020 - 5:04:34 PM
Last modification on : Wednesday, January 19, 2022 - 1:50:05 PM
Long-term archiving on: : Thursday, April 23, 2020 - 5:20:04 PM


 Restricted access
To satisfy the distribution rights of the publisher, the document is embargoed until : jamais

Please log in to resquest access to the document



Sabrina Bondu, Anne-Sophie Alary, Carine Lefevre, Alexandre Houy, Grace Jung, et al.. A variant erythroferrone disrupts iron homeostasis in SF3B1-mutated myelodysplastic syndrome. Science Translational Medicine, American Association for the Advancement of Science, 2019, 11 (500), pp.eaav5467. ⟨10.1126/scitranslmed.aav5467⟩. ⟨inserm-02449216⟩



Les métriques sont temporairement indisponibles