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An unexpected alliance between stress responses to drive oncogenesis

XBP1 is a well-characterized regulator of the unfolding protein response that is activated in response to unfolded or misfolded proteins or nutrient deprivation. The conventional wisdom is that XBP1 is activated to coordinate the unfolded protein response and promote cellular survival under stresses...

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Detalles Bibliográficos
Autores principales: Keenan, Melissa M, Ding, Chien-Kuang Cornelia, Chi, Jen-Tsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429501/
https://www.ncbi.nlm.nih.gov/pubmed/25927911
http://dx.doi.org/10.1186/s13058-014-0471-1
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author Keenan, Melissa M
Ding, Chien-Kuang Cornelia
Chi, Jen-Tsan
author_facet Keenan, Melissa M
Ding, Chien-Kuang Cornelia
Chi, Jen-Tsan
author_sort Keenan, Melissa M
collection PubMed
description XBP1 is a well-characterized regulator of the unfolding protein response that is activated in response to unfolded or misfolded proteins or nutrient deprivation. The conventional wisdom is that XBP1 is activated to coordinate the unfolded protein response and promote cellular survival under stresses. A recent study provides intriguing evidence that, in triple-negative breast cancer, XBP1 plays a major role in promoting oncogenesis and cancer stem cell properties. Unexpectedly, XBP1 accomplishes this by recruiting hypoxia-inducible factor 1α and activating oncogenic transcriptional programs. This study reveals a surprising hierarchy and alliance between two stress regulators with distinct transcriptional outputs to promote an aggressive oncogenic state.
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spelling pubmed-44295012015-05-14 An unexpected alliance between stress responses to drive oncogenesis Keenan, Melissa M Ding, Chien-Kuang Cornelia Chi, Jen-Tsan Breast Cancer Res Viewpoint XBP1 is a well-characterized regulator of the unfolding protein response that is activated in response to unfolded or misfolded proteins or nutrient deprivation. The conventional wisdom is that XBP1 is activated to coordinate the unfolded protein response and promote cellular survival under stresses. A recent study provides intriguing evidence that, in triple-negative breast cancer, XBP1 plays a major role in promoting oncogenesis and cancer stem cell properties. Unexpectedly, XBP1 accomplishes this by recruiting hypoxia-inducible factor 1α and activating oncogenic transcriptional programs. This study reveals a surprising hierarchy and alliance between two stress regulators with distinct transcriptional outputs to promote an aggressive oncogenic state. BioMed Central 2014-11-06 2014 /pmc/articles/PMC4429501/ /pubmed/25927911 http://dx.doi.org/10.1186/s13058-014-0471-1 Text en © Keenan et al.; licensee BioMed Central Ltd. 2014 The licensee has exclusive rights to distribute this article, in any medium, for 6 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Viewpoint
Keenan, Melissa M
Ding, Chien-Kuang Cornelia
Chi, Jen-Tsan
An unexpected alliance between stress responses to drive oncogenesis
title An unexpected alliance between stress responses to drive oncogenesis
title_full An unexpected alliance between stress responses to drive oncogenesis
title_fullStr An unexpected alliance between stress responses to drive oncogenesis
title_full_unstemmed An unexpected alliance between stress responses to drive oncogenesis
title_short An unexpected alliance between stress responses to drive oncogenesis
title_sort unexpected alliance between stress responses to drive oncogenesis
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429501/
https://www.ncbi.nlm.nih.gov/pubmed/25927911
http://dx.doi.org/10.1186/s13058-014-0471-1
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