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PHD2: from hypoxia regulation to disease progression

Oxygen represents one of the major molecules required for the development and maintenance of life. An adequate response to hypoxia is therefore required for the functioning of the majority of living organisms and relies on the activation of the hypoxia-inducible factor (HIF) pathway. HIF prolyl hydr...

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Autores principales: Meneses, Ana M, Wielockx, Ben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5085284/
https://www.ncbi.nlm.nih.gov/pubmed/27800508
http://dx.doi.org/10.2147/HP.S53576
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author Meneses, Ana M
Wielockx, Ben
author_facet Meneses, Ana M
Wielockx, Ben
author_sort Meneses, Ana M
collection PubMed
description Oxygen represents one of the major molecules required for the development and maintenance of life. An adequate response to hypoxia is therefore required for the functioning of the majority of living organisms and relies on the activation of the hypoxia-inducible factor (HIF) pathway. HIF prolyl hydroxylase domain-2 (PHD2) has long been recognized as the major regulator of this response, controlling a myriad of outcomes that range from cell death to proliferation. However, this enzyme has been associated with more pathways, making the role of this protein remarkably complex under distinct pathologies. While a protective role seems to exist in physiological conditions such as erythropoiesis; the picture is more complex during pathologies such as cancer. Since the regulation of this enzyme and its closest family members is currently considered as a possible therapy for various diseases, understanding the different particular roles of this protein is essential.
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spelling pubmed-50852842016-10-31 PHD2: from hypoxia regulation to disease progression Meneses, Ana M Wielockx, Ben Hypoxia (Auckl) Review Oxygen represents one of the major molecules required for the development and maintenance of life. An adequate response to hypoxia is therefore required for the functioning of the majority of living organisms and relies on the activation of the hypoxia-inducible factor (HIF) pathway. HIF prolyl hydroxylase domain-2 (PHD2) has long been recognized as the major regulator of this response, controlling a myriad of outcomes that range from cell death to proliferation. However, this enzyme has been associated with more pathways, making the role of this protein remarkably complex under distinct pathologies. While a protective role seems to exist in physiological conditions such as erythropoiesis; the picture is more complex during pathologies such as cancer. Since the regulation of this enzyme and its closest family members is currently considered as a possible therapy for various diseases, understanding the different particular roles of this protein is essential. Dove Medical Press 2016-04-11 /pmc/articles/PMC5085284/ /pubmed/27800508 http://dx.doi.org/10.2147/HP.S53576 Text en © 2016 Meneses and Wielockx. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Meneses, Ana M
Wielockx, Ben
PHD2: from hypoxia regulation to disease progression
title PHD2: from hypoxia regulation to disease progression
title_full PHD2: from hypoxia regulation to disease progression
title_fullStr PHD2: from hypoxia regulation to disease progression
title_full_unstemmed PHD2: from hypoxia regulation to disease progression
title_short PHD2: from hypoxia regulation to disease progression
title_sort phd2: from hypoxia regulation to disease progression
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5085284/
https://www.ncbi.nlm.nih.gov/pubmed/27800508
http://dx.doi.org/10.2147/HP.S53576
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