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Molecular and therapeutic frontiers in anemia therapy
Nilesh Rai, Omar Abdel-Wahab, Lingbo Zhang
Nilesh Rai, Omar Abdel-Wahab, Lingbo Zhang
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Review

Molecular and therapeutic frontiers in anemia therapy

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Abstract

Anemia affects one-third of the population globally and is marked by impaired erythropoiesis that results in substantial mortality and morbidity. Over the past few decades, our understanding of the molecular mechanisms underlying anemia has progressed but translating that knowledge into effective targeted therapeutics remains challenging. Preclinical and clinical studies substantiate the efficacy of modulating erythropoietin-driven signaling pathways to stimulate erythropoiesis. Additional approaches include strategies to maintain iron homeostasis and control iron metabolism, using small molecules and oral supplements. New frontiers in molecular regulation of anemia include perturbation of regulatory genes and spliceosome proteins in erythroid cells, as well as mutation-specific therapeutic approaches. Finally, new evidence supporting the importance of neuronal signaling and mitochondrial dynamics in shaping erythropoiesis is pointing toward novel interventions. Here, we discuss the molecular and genetic factors underlying defective erythropoiesis and highlight current and emerging therapies, including molecular targets to overcome drug resistance.

Authors

Nilesh Rai, Omar Abdel-Wahab, Lingbo Zhang

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Figure 1

Signal transduction–based therapies for anemia.

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Signal transduction–based therapies for anemia.
(A) Erythropoietin-media...
(A) Erythropoietin-mediated (EPO-mediated) key signaling pathways regulate erythroid progenitor differentiation and maturation. EPO interacts with its receptor (EPO-R), phosphorylating JAK2 and activating downstream STAT5, MAPK, and PI3K/Akt transduction pathways, which promote cell division, maturation, and proliferation. KLF, Krüppel-like factor. (B) Luspatercept-mediated inhibition of the SMAD2/3 pathway. Luspatercept traps ligands such as activin B and GDF11, inhibiting their interaction with activin receptor type IIB. This prevents the phosphorylation of Smad2/3 and their binding to the coactivator Smad4, thereby activating late-stage erythroid-specific genes and promoting erythropoiesis by inhibiting Smad2/3 signaling in transfusion-dependent anemia. ActRIIB, activin receptor type IIB; GDF11, growth differentiation factor 11.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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