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STAT5 as a Key Protein of Erythropoietin Signalization

Erythropoietin (EPO) acts on multiple tissues through its receptor EPOR, a member of a cytokine class I receptor superfamily with pleiotropic effects. The interaction of EPO and EPOR triggers the activation of several signaling pathways that induce erythropoiesis, including JAK2/STAT5, PI3K/AKT, and...

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Detalles Bibliográficos
Autores principales: Tóthová, Zuzana, Tomc, Jana, Debeljak, Nataša, Solár, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268974/
https://www.ncbi.nlm.nih.gov/pubmed/34281163
http://dx.doi.org/10.3390/ijms22137109
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author Tóthová, Zuzana
Tomc, Jana
Debeljak, Nataša
Solár, Peter
author_facet Tóthová, Zuzana
Tomc, Jana
Debeljak, Nataša
Solár, Peter
author_sort Tóthová, Zuzana
collection PubMed
description Erythropoietin (EPO) acts on multiple tissues through its receptor EPOR, a member of a cytokine class I receptor superfamily with pleiotropic effects. The interaction of EPO and EPOR triggers the activation of several signaling pathways that induce erythropoiesis, including JAK2/STAT5, PI3K/AKT, and MAPK. The canonical EPOR/JAK2/STAT5 pathway is a known regulator of differentiation, proliferation, and cell survival of erythroid progenitors. In addition, its role in the protection of other cells, including cancer cells, is under intense investigation. The involvement of EPOR/JAK2/STAT5 in other processes such as mRNA splicing, cytoskeleton reorganization, and cell metabolism has been recently described. The transcriptomics, proteomics, and epigenetic studies reviewed in this article provide a detailed understanding of EPO signalization. Advances in this area of research may be useful for improving the efficacy of EPO therapy in hematologic disorders, as well as in cancer treatment.
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spelling pubmed-82689742021-07-10 STAT5 as a Key Protein of Erythropoietin Signalization Tóthová, Zuzana Tomc, Jana Debeljak, Nataša Solár, Peter Int J Mol Sci Review Erythropoietin (EPO) acts on multiple tissues through its receptor EPOR, a member of a cytokine class I receptor superfamily with pleiotropic effects. The interaction of EPO and EPOR triggers the activation of several signaling pathways that induce erythropoiesis, including JAK2/STAT5, PI3K/AKT, and MAPK. The canonical EPOR/JAK2/STAT5 pathway is a known regulator of differentiation, proliferation, and cell survival of erythroid progenitors. In addition, its role in the protection of other cells, including cancer cells, is under intense investigation. The involvement of EPOR/JAK2/STAT5 in other processes such as mRNA splicing, cytoskeleton reorganization, and cell metabolism has been recently described. The transcriptomics, proteomics, and epigenetic studies reviewed in this article provide a detailed understanding of EPO signalization. Advances in this area of research may be useful for improving the efficacy of EPO therapy in hematologic disorders, as well as in cancer treatment. MDPI 2021-07-01 /pmc/articles/PMC8268974/ /pubmed/34281163 http://dx.doi.org/10.3390/ijms22137109 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tóthová, Zuzana
Tomc, Jana
Debeljak, Nataša
Solár, Peter
STAT5 as a Key Protein of Erythropoietin Signalization
title STAT5 as a Key Protein of Erythropoietin Signalization
title_full STAT5 as a Key Protein of Erythropoietin Signalization
title_fullStr STAT5 as a Key Protein of Erythropoietin Signalization
title_full_unstemmed STAT5 as a Key Protein of Erythropoietin Signalization
title_short STAT5 as a Key Protein of Erythropoietin Signalization
title_sort stat5 as a key protein of erythropoietin signalization
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268974/
https://www.ncbi.nlm.nih.gov/pubmed/34281163
http://dx.doi.org/10.3390/ijms22137109
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