Iron chelating properties of Eltrombopag: Investigating its role in thalassemia-induced osteoporosis.
basic_science · Level V
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- Record sourced from PubMed, PMID 30507954.
- Also identified by DOI 10.1371/journal.pone.0208102 and PMC identifier 6277068.
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Abstract
Chronic blood transfusions are responsible to cause iron overload, which leads to several complications to end organs and osteoporosis. Iron chelation is needed to remove iron excess and to contain bone-mass loss. Deferasirox is the most recent oral iron chelator that prevents transfusion related iron overload complications. Recently Eltrombopag (ELT) iron chelating properties are emerging. ELT is an agonist at Thrombopoietin receptor, used in treatment of thrombocytopenia. We tested ELT and Deferasirox in iron overloaded osteoclasts from thalassemic patients and donors measuring intracellular iron, TRAP expression and osteoclast activity. We confirmed ELT iron chelation capacity also in bone tissue and a synergic effect when used with Deferasirox. Moreover, having demonstrated its effects on osteoclast activity, we suggest for the first time that ELT could ameliorate bone tissue's health reducing bone mass loss.
Medical subject headings
- Benzoates
- Hydrazines
- Iron Chelating Agents
- Iron Overload
- Osteoporosis
- Pyrazoles
- Thalassemia
- Transfusion Reaction