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Molecular Crosstalk Between MYC and HIF in Cancer

The transcription factor c-MYC (MYC thereafter) is a global regulator of gene expression. It is overexpressed or deregulated in human cancers of diverse origins and plays a key role in the development of cancers. Hypoxia-inducible factors (HIFs), a central regulator for cells to adapt to low cellula...

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Autores principales: Li, Yanping, Sun, Xiao-Xin, Qian, David Z., Dai, Mu-Shui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676913/
https://www.ncbi.nlm.nih.gov/pubmed/33251216
http://dx.doi.org/10.3389/fcell.2020.590576
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author Li, Yanping
Sun, Xiao-Xin
Qian, David Z.
Dai, Mu-Shui
author_facet Li, Yanping
Sun, Xiao-Xin
Qian, David Z.
Dai, Mu-Shui
author_sort Li, Yanping
collection PubMed
description The transcription factor c-MYC (MYC thereafter) is a global regulator of gene expression. It is overexpressed or deregulated in human cancers of diverse origins and plays a key role in the development of cancers. Hypoxia-inducible factors (HIFs), a central regulator for cells to adapt to low cellular oxygen levels, is also often overexpressed and activated in many human cancers. HIF mediates the primary transcriptional response of a wide range of genes in response to hypoxia. Earlier studies focused on the inhibition of MYC by HIF during hypoxia, when MYC is expressed at physiological level, to help cells survive under low oxygen conditions. Emerging evidence suggests that MYC and HIF also cooperate to promote cancer cell growth and progression. This review will summarize the current understanding of the complex molecular interplay between MYC and HIF.
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spelling pubmed-76769132020-11-27 Molecular Crosstalk Between MYC and HIF in Cancer Li, Yanping Sun, Xiao-Xin Qian, David Z. Dai, Mu-Shui Front Cell Dev Biol Cell and Developmental Biology The transcription factor c-MYC (MYC thereafter) is a global regulator of gene expression. It is overexpressed or deregulated in human cancers of diverse origins and plays a key role in the development of cancers. Hypoxia-inducible factors (HIFs), a central regulator for cells to adapt to low cellular oxygen levels, is also often overexpressed and activated in many human cancers. HIF mediates the primary transcriptional response of a wide range of genes in response to hypoxia. Earlier studies focused on the inhibition of MYC by HIF during hypoxia, when MYC is expressed at physiological level, to help cells survive under low oxygen conditions. Emerging evidence suggests that MYC and HIF also cooperate to promote cancer cell growth and progression. This review will summarize the current understanding of the complex molecular interplay between MYC and HIF. Frontiers Media S.A. 2020-11-05 /pmc/articles/PMC7676913/ /pubmed/33251216 http://dx.doi.org/10.3389/fcell.2020.590576 Text en Copyright © 2020 Li, Sun, Qian and Dai. 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) and the copyright owner(s) 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 Cell and Developmental Biology
Li, Yanping
Sun, Xiao-Xin
Qian, David Z.
Dai, Mu-Shui
Molecular Crosstalk Between MYC and HIF in Cancer
title Molecular Crosstalk Between MYC and HIF in Cancer
title_full Molecular Crosstalk Between MYC and HIF in Cancer
title_fullStr Molecular Crosstalk Between MYC and HIF in Cancer
title_full_unstemmed Molecular Crosstalk Between MYC and HIF in Cancer
title_short Molecular Crosstalk Between MYC and HIF in Cancer
title_sort molecular crosstalk between myc and hif in cancer
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676913/
https://www.ncbi.nlm.nih.gov/pubmed/33251216
http://dx.doi.org/10.3389/fcell.2020.590576
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