Literature DB >> 26919168

New strategies to target iron metabolism for the treatment of beta thalassemia.

Paraskevi Rea Oikonomidou1, Carla Casu1, Stefano Rivella1,2.   

Abstract

Iron is one of the most abundant elements in the Earth and a fundamental component of enzymes and other proteins that participate in a wide range of biological processes. As the human body has no mechanisms to eliminate the excess of iron, its metabolism needs to be tightly controlled in order to avoid all the sequelae associated with high iron levels. Iron overload is the main cause of morbidity and mortality in beta thalassemia. The master regulator of iron homeostasis, hepcidin, is chronically repressed in this disorder, leading to increased intestinal iron absorption and consequent iron overload. Many groups have focused on obtaining a better understanding of the pathways involved in iron regulation. New molecules have recently been synthesized and used in animal models of dysregulated iron metabolism, demonstrating their ability to target and reduce iron load. Antisense oligonucleotides, as well as lipid nanoparticle-formulated small interfering RNAs and minihepcidins peptides, are novel agents that have already proved to be efficient in modulating iron metabolism in mouse models and are therefore promising candidates for the treatment of patients affected by iron disorders.
© 2016 New York Academy of Sciences.

Entities:  

Keywords:  beta thalassemia; iron metabolism; iron overload; red blood cells

Mesh:

Substances:

Year:  2016        PMID: 26919168      PMCID: PMC5271577          DOI: 10.1111/nyas.13018

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  83 in total

1.  Plasma and red cell iron turnover in normal subjects and in patients having various hematopoietic disorders.

Authors:  R L HUFF; T G HENNESSY; R E AUSTIN; J F GARCIA; B M ROBERTS; J H LAWRENCE
Journal:  J Clin Invest       Date:  1950-08       Impact factor: 14.808

2.  Stimulated erythropoiesis with secondary iron loading leads to a decrease in hepcidin despite an increase in bone morphogenetic protein 6 expression.

Authors:  David M Frazer; Sarah J Wilkins; Deepak Darshan; Alison C Badrick; Gordon D McLaren; Gregory J Anderson
Journal:  Br J Haematol       Date:  2012-03-26       Impact factor: 6.998

3.  Iron absorption and loading in beta-thalassaemia intermedia.

Authors:  M J Pippard; S T Callender; G T Warner; D J Weatherall
Journal:  Lancet       Date:  1979-10-20       Impact factor: 79.321

4.  Minihepcidins prevent iron overload in a hepcidin-deficient mouse model of severe hemochromatosis.

Authors:  Emilio Ramos; Piotr Ruchala; Julia B Goodnough; Léon Kautz; Gloria C Preza; Elizabeta Nemeth; Tomas Ganz
Journal:  Blood       Date:  2012-09-18       Impact factor: 22.113

5.  The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation.

Authors:  Gaël Nicolas; Caroline Chauvet; Lydie Viatte; Jean Louis Danan; Xavier Bigard; Isabelle Devaux; Carole Beaumont; Axel Kahn; Sophie Vaulont
Journal:  J Clin Invest       Date:  2002-10       Impact factor: 14.808

6.  Hepcidin in iron overload disorders.

Authors:  George Papanikolaou; Michalis Tzilianos; John I Christakis; Dionisios Bogdanos; Konstantina Tsimirika; Julie MacFarlane; Y Paul Goldberg; Nikos Sakellaropoulos; Tomas Ganz; Elizabeta Nemeth
Journal:  Blood       Date:  2005-01-25       Impact factor: 22.113

7.  Accelerated programmed cell death (apoptosis) in erythroid precursors of patients with severe beta-thalassemia (Cooley's anemia)

Authors:  J Yuan; E Angelucci; G Lucarelli; M Aljurf; L M Snyder; C R Kiefer; L Ma; S L Schrier
Journal:  Blood       Date:  1993-07-15       Impact factor: 22.113

8.  Liver iron concentrations and urinary hepcidin in beta-thalassemia.

Authors:  Raffaella Origa; Renzo Galanello; Tomas Ganz; Nicolina Giagu; Liliana Maccioni; Gavino Faa; Elizabeta Nemeth
Journal:  Haematologica       Date:  2007-05       Impact factor: 9.941

Review 9.  Beta-thalassemia.

Authors:  Antonio Cao; Renzo Galanello
Journal:  Genet Med       Date:  2010-02       Impact factor: 8.822

10.  The serine protease matriptase-2 (TMPRSS6) inhibits hepcidin activation by cleaving membrane hemojuvelin.

Authors:  Laura Silvestri; Alessia Pagani; Antonella Nai; Ivana De Domenico; Jerry Kaplan; Clara Camaschella
Journal:  Cell Metab       Date:  2008-10-30       Impact factor: 27.287

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  7 in total

1.  New potential players in hepcidin regulation.

Authors:  Maxwell Chappell; Stefano Rivella
Journal:  Haematologica       Date:  2019-09       Impact factor: 9.941

Review 2.  Hepcidin agonists as therapeutic tools.

Authors:  Carla Casu; Elizabeta Nemeth; Stefano Rivella
Journal:  Blood       Date:  2018-03-09       Impact factor: 22.113

Review 3.  β-Thalassemia.

Authors:  Raffaella Origa
Journal:  Genet Med       Date:  2016-11-03       Impact factor: 8.822

Review 4.  Beta Thalassemia: New Therapeutic Options Beyond Transfusion and Iron Chelation.

Authors:  Irene Motta; Rayan Bou-Fakhredin; Ali T Taher; Maria Domenica Cappellini
Journal:  Drugs       Date:  2020-07       Impact factor: 9.546

Review 5.  Molecular genetics of β-thalassemia: A narrative review.

Authors:  Tang-Her Jaing; Tsung-Yen Chang; Shih-Hsiang Chen; Chen-Wei Lin; Yu-Chuan Wen; Chia-Chi Chiu
Journal:  Medicine (Baltimore)       Date:  2021-11-12       Impact factor: 1.817

6.  Oral ferroportin inhibitor VIT-2763: First-in-human, phase 1 study in healthy volunteers.

Authors:  Frank Richard; Jan Jaap van Lier; Bernard Roubert; Teba Haboubi; Udo-Michael Göhring; Franz Dürrenberger
Journal:  Am J Hematol       Date:  2019-11-19       Impact factor: 10.047

7.  A farewell to phlebotomy-use of placenta-derived drugs Laennec and Porcine for improving hereditary hemochromatosis without phlebotomy: a case report.

Authors:  Yuki Hamada; Eiichi Hirano; Koji Sugimoto; Keizo Hanada; Taiichi Kaku; Naoki Manda; Kenichi Tsuchida
Journal:  J Med Case Rep       Date:  2022-01-23
  7 in total

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