Regulation of erythropoietin production and recent trends in anaemia therapy

Detalhes bibliográficos
Autor(a) principal: Almeida,Filipa
Data de Publicação: 2015
Outros Autores: Santos,Sofia, Beirão,Idalina
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692015000200003
Resumo: About 30 years ago, the treatment of chronic renal disease anaemia was revolutionized by the introduction of recombinant human erythropoietin, which reduced the need for blood transfusions. In spite of this huge advance, the first recombinant human erythropoietin has a relatively short half-life and needs to be administered two to three times per week. Subsequently, other molecules were developed, such as darbepoetin alfa, continuous erythropoietin receptor activator (CERA) and peginesatide, with longer half-life, but the route of administration still remains a problem. Erythropoietin has an action that exceeds erythropoiesis and plays an important role in cell protection. Based on knowledge of the molecular mechanisms that control erythropoiesis, namely the regulation of EPO gene expression, through HIF system, GATA-2 and NF-kB, several upcoming therapeutic agents and strategies for stimulating and treating anaemia emerged. The main effort in developing these treatments is to achieve other routes of administration, more convenient for the patient, such as oral therapy, not disregarding an easier production, storage and frequency of administration. Some of them are still in laboratory phase and others already in clinical trials phase II or III. In this work, based on a literature search of studies using MEDLINE, our objective is to review the regulation of erythropoietin production and its functions, as well as treatment approach for anaemia of chronic kidney disease, with particular focus on new therapies
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spelling Regulation of erythropoietin production and recent trends in anaemia therapyAnaemiaerythropoietinGATA-2 inhibitorshepcidinhypoxia-inducible factorskidney diseaseAbout 30 years ago, the treatment of chronic renal disease anaemia was revolutionized by the introduction of recombinant human erythropoietin, which reduced the need for blood transfusions. In spite of this huge advance, the first recombinant human erythropoietin has a relatively short half-life and needs to be administered two to three times per week. Subsequently, other molecules were developed, such as darbepoetin alfa, continuous erythropoietin receptor activator (CERA) and peginesatide, with longer half-life, but the route of administration still remains a problem. Erythropoietin has an action that exceeds erythropoiesis and plays an important role in cell protection. Based on knowledge of the molecular mechanisms that control erythropoiesis, namely the regulation of EPO gene expression, through HIF system, GATA-2 and NF-kB, several upcoming therapeutic agents and strategies for stimulating and treating anaemia emerged. The main effort in developing these treatments is to achieve other routes of administration, more convenient for the patient, such as oral therapy, not disregarding an easier production, storage and frequency of administration. Some of them are still in laboratory phase and others already in clinical trials phase II or III. In this work, based on a literature search of studies using MEDLINE, our objective is to review the regulation of erythropoietin production and its functions, as well as treatment approach for anaemia of chronic kidney disease, with particular focus on new therapiesSociedade Portuguesa de Nefrologia2015-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692015000200003Portuguese Journal of Nephrology & Hypertension v.29 n.2 2015reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692015000200003Almeida,FilipaSantos,SofiaBeirão,Idalinainfo:eu-repo/semantics/openAccess2024-02-06T17:04:48Zoai:scielo:S0872-01692015000200003Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:18:54.464150Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Regulation of erythropoietin production and recent trends in anaemia therapy
title Regulation of erythropoietin production and recent trends in anaemia therapy
spellingShingle Regulation of erythropoietin production and recent trends in anaemia therapy
Almeida,Filipa
Anaemia
erythropoietin
GATA-2 inhibitors
hepcidin
hypoxia-inducible factors
kidney disease
title_short Regulation of erythropoietin production and recent trends in anaemia therapy
title_full Regulation of erythropoietin production and recent trends in anaemia therapy
title_fullStr Regulation of erythropoietin production and recent trends in anaemia therapy
title_full_unstemmed Regulation of erythropoietin production and recent trends in anaemia therapy
title_sort Regulation of erythropoietin production and recent trends in anaemia therapy
author Almeida,Filipa
author_facet Almeida,Filipa
Santos,Sofia
Beirão,Idalina
author_role author
author2 Santos,Sofia
Beirão,Idalina
author2_role author
author
dc.contributor.author.fl_str_mv Almeida,Filipa
Santos,Sofia
Beirão,Idalina
dc.subject.por.fl_str_mv Anaemia
erythropoietin
GATA-2 inhibitors
hepcidin
hypoxia-inducible factors
kidney disease
topic Anaemia
erythropoietin
GATA-2 inhibitors
hepcidin
hypoxia-inducible factors
kidney disease
description About 30 years ago, the treatment of chronic renal disease anaemia was revolutionized by the introduction of recombinant human erythropoietin, which reduced the need for blood transfusions. In spite of this huge advance, the first recombinant human erythropoietin has a relatively short half-life and needs to be administered two to three times per week. Subsequently, other molecules were developed, such as darbepoetin alfa, continuous erythropoietin receptor activator (CERA) and peginesatide, with longer half-life, but the route of administration still remains a problem. Erythropoietin has an action that exceeds erythropoiesis and plays an important role in cell protection. Based on knowledge of the molecular mechanisms that control erythropoiesis, namely the regulation of EPO gene expression, through HIF system, GATA-2 and NF-kB, several upcoming therapeutic agents and strategies for stimulating and treating anaemia emerged. The main effort in developing these treatments is to achieve other routes of administration, more convenient for the patient, such as oral therapy, not disregarding an easier production, storage and frequency of administration. Some of them are still in laboratory phase and others already in clinical trials phase II or III. In this work, based on a literature search of studies using MEDLINE, our objective is to review the regulation of erythropoietin production and its functions, as well as treatment approach for anaemia of chronic kidney disease, with particular focus on new therapies
publishDate 2015
dc.date.none.fl_str_mv 2015-06-01
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dc.identifier.uri.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692015000200003
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dc.language.iso.fl_str_mv eng
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dc.publisher.none.fl_str_mv Sociedade Portuguesa de Nefrologia
publisher.none.fl_str_mv Sociedade Portuguesa de Nefrologia
dc.source.none.fl_str_mv Portuguese Journal of Nephrology & Hypertension v.29 n.2 2015
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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