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HIF1-alpha expressing cells induce a hypoxic-like response in neighbouring cancer cells

BACKGROUND: Hypoxia stimulates metastasis in cancer and is linked to poor patient prognosis. In tumours, oxygen levels vary and hypoxic regions exist within a generally well-oxygenated tumour. However, whilst the heterogeneous environment is known to contribute to metastatic progression, little is k...

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Autores principales: Harrison, Hannah, Pegg, Henry J., Thompson, Jamie, Bates, Christian, Shore, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011406/
https://www.ncbi.nlm.nih.gov/pubmed/29925335
http://dx.doi.org/10.1186/s12885-018-4577-1
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author Harrison, Hannah
Pegg, Henry J.
Thompson, Jamie
Bates, Christian
Shore, Paul
author_facet Harrison, Hannah
Pegg, Henry J.
Thompson, Jamie
Bates, Christian
Shore, Paul
author_sort Harrison, Hannah
collection PubMed
description BACKGROUND: Hypoxia stimulates metastasis in cancer and is linked to poor patient prognosis. In tumours, oxygen levels vary and hypoxic regions exist within a generally well-oxygenated tumour. However, whilst the heterogeneous environment is known to contribute to metastatic progression, little is known about the mechanism by which heterogeneic hypoxia contributes to cancer progression. This is largely because existing experimental models do not recapitulate the heterogeneous nature of hypoxia. The primary effector of the hypoxic response is the transcription factor Hypoxia inducible factor 1-alpha (HIF1-alpha). HIF1-alpha is stabilised in response to low oxygen levels in the cellular environment and its expression is seen in hypoxic regions throughout the tumour. METHODS: We have developed a model system in which HIF1-alpha can be induced within a sub-population of cancer cells, thus enabling us to mimic the effects of heterogeneic HIF1-alpha expression. RESULTS: We show that induction of HIF1-alpha not only recapitulates elements of the hypoxic response in the induced cells but also results in significant changes in proliferation, gene expression and mammosphere formation within the HIF1-alpha negative population. CONCLUSIONS: These findings suggest that the HIF1-alpha expressing cells found within hypoxic regions are likely to contribute to the subsequent progression of a tumour by modifying the behaviour of cells in the non-hypoxic regions of the local micro-environment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4577-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-60114062018-07-05 HIF1-alpha expressing cells induce a hypoxic-like response in neighbouring cancer cells Harrison, Hannah Pegg, Henry J. Thompson, Jamie Bates, Christian Shore, Paul BMC Cancer Research Article BACKGROUND: Hypoxia stimulates metastasis in cancer and is linked to poor patient prognosis. In tumours, oxygen levels vary and hypoxic regions exist within a generally well-oxygenated tumour. However, whilst the heterogeneous environment is known to contribute to metastatic progression, little is known about the mechanism by which heterogeneic hypoxia contributes to cancer progression. This is largely because existing experimental models do not recapitulate the heterogeneous nature of hypoxia. The primary effector of the hypoxic response is the transcription factor Hypoxia inducible factor 1-alpha (HIF1-alpha). HIF1-alpha is stabilised in response to low oxygen levels in the cellular environment and its expression is seen in hypoxic regions throughout the tumour. METHODS: We have developed a model system in which HIF1-alpha can be induced within a sub-population of cancer cells, thus enabling us to mimic the effects of heterogeneic HIF1-alpha expression. RESULTS: We show that induction of HIF1-alpha not only recapitulates elements of the hypoxic response in the induced cells but also results in significant changes in proliferation, gene expression and mammosphere formation within the HIF1-alpha negative population. CONCLUSIONS: These findings suggest that the HIF1-alpha expressing cells found within hypoxic regions are likely to contribute to the subsequent progression of a tumour by modifying the behaviour of cells in the non-hypoxic regions of the local micro-environment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4577-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-20 /pmc/articles/PMC6011406/ /pubmed/29925335 http://dx.doi.org/10.1186/s12885-018-4577-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Harrison, Hannah
Pegg, Henry J.
Thompson, Jamie
Bates, Christian
Shore, Paul
HIF1-alpha expressing cells induce a hypoxic-like response in neighbouring cancer cells
title HIF1-alpha expressing cells induce a hypoxic-like response in neighbouring cancer cells
title_full HIF1-alpha expressing cells induce a hypoxic-like response in neighbouring cancer cells
title_fullStr HIF1-alpha expressing cells induce a hypoxic-like response in neighbouring cancer cells
title_full_unstemmed HIF1-alpha expressing cells induce a hypoxic-like response in neighbouring cancer cells
title_short HIF1-alpha expressing cells induce a hypoxic-like response in neighbouring cancer cells
title_sort hif1-alpha expressing cells induce a hypoxic-like response in neighbouring cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011406/
https://www.ncbi.nlm.nih.gov/pubmed/29925335
http://dx.doi.org/10.1186/s12885-018-4577-1
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