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Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer

Hypoxia-inducible factor 1 alpha (HIF-1α) orchestrates cellular adaptation to low oxygen and nutrient-deprived environment and drives progression to malignancy in human solid cancers. Its canonical regulation involves prolyl hydroxylases (PHDs), which in normoxia induce degradation, whereas in hypox...

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Autores principales: Iommarini, Luisa, Porcelli, Anna Maria, Gasparre, Giuseppe, Kurelac, Ivana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711814/
https://www.ncbi.nlm.nih.gov/pubmed/29230384
http://dx.doi.org/10.3389/fonc.2017.00286
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author Iommarini, Luisa
Porcelli, Anna Maria
Gasparre, Giuseppe
Kurelac, Ivana
author_facet Iommarini, Luisa
Porcelli, Anna Maria
Gasparre, Giuseppe
Kurelac, Ivana
author_sort Iommarini, Luisa
collection PubMed
description Hypoxia-inducible factor 1 alpha (HIF-1α) orchestrates cellular adaptation to low oxygen and nutrient-deprived environment and drives progression to malignancy in human solid cancers. Its canonical regulation involves prolyl hydroxylases (PHDs), which in normoxia induce degradation, whereas in hypoxia allow stabilization of HIF-1α. However, in certain circumstances, HIF-1α regulation goes beyond the actual external oxygen levels and involves PHD-independent mechanisms. Here, we gather and discuss the evidence on the non-canonical HIF-1α regulation, focusing in particular on the consequences of mitochondrial respiratory complexes damage on stabilization of this pleiotropic transcription factor.
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spelling pubmed-57118142017-12-11 Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer Iommarini, Luisa Porcelli, Anna Maria Gasparre, Giuseppe Kurelac, Ivana Front Oncol Oncology Hypoxia-inducible factor 1 alpha (HIF-1α) orchestrates cellular adaptation to low oxygen and nutrient-deprived environment and drives progression to malignancy in human solid cancers. Its canonical regulation involves prolyl hydroxylases (PHDs), which in normoxia induce degradation, whereas in hypoxia allow stabilization of HIF-1α. However, in certain circumstances, HIF-1α regulation goes beyond the actual external oxygen levels and involves PHD-independent mechanisms. Here, we gather and discuss the evidence on the non-canonical HIF-1α regulation, focusing in particular on the consequences of mitochondrial respiratory complexes damage on stabilization of this pleiotropic transcription factor. Frontiers Media S.A. 2017-11-27 /pmc/articles/PMC5711814/ /pubmed/29230384 http://dx.doi.org/10.3389/fonc.2017.00286 Text en Copyright © 2017 Iommarini, Porcelli, Gasparre and Kurelac. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Iommarini, Luisa
Porcelli, Anna Maria
Gasparre, Giuseppe
Kurelac, Ivana
Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer
title Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer
title_full Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer
title_fullStr Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer
title_full_unstemmed Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer
title_short Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer
title_sort non-canonical mechanisms regulating hypoxia-inducible factor 1 alpha in cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711814/
https://www.ncbi.nlm.nih.gov/pubmed/29230384
http://dx.doi.org/10.3389/fonc.2017.00286
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