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IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling

Activation of endoplasmic reticulum (ER) stress/the unfolded protein response (UPR) has been linked to cancer, but the molecular mechanisms are poorly understood and there is a paucity of reagents to translate this for cancer therapy. Here, we report that an IRE1α RNase-specific inhibitor, MKC8866,...

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Autores principales: Sheng, Xia, Nenseth, Hatice Zeynep, Qu, Su, Kuzu, Omer F., Frahnow, Turid, Simon, Lukas, Greene, Stephanie, Zeng, Qingping, Fazli, Ladan, Rennie, Paul S., Mills, Ian G., Danielsen, Håvard, Theis, Fabian, Patterson, John B., Jin, Yang, Saatcioglu, Fahri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345973/
https://www.ncbi.nlm.nih.gov/pubmed/30679434
http://dx.doi.org/10.1038/s41467-018-08152-3
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author Sheng, Xia
Nenseth, Hatice Zeynep
Qu, Su
Kuzu, Omer F.
Frahnow, Turid
Simon, Lukas
Greene, Stephanie
Zeng, Qingping
Fazli, Ladan
Rennie, Paul S.
Mills, Ian G.
Danielsen, Håvard
Theis, Fabian
Patterson, John B.
Jin, Yang
Saatcioglu, Fahri
author_facet Sheng, Xia
Nenseth, Hatice Zeynep
Qu, Su
Kuzu, Omer F.
Frahnow, Turid
Simon, Lukas
Greene, Stephanie
Zeng, Qingping
Fazli, Ladan
Rennie, Paul S.
Mills, Ian G.
Danielsen, Håvard
Theis, Fabian
Patterson, John B.
Jin, Yang
Saatcioglu, Fahri
author_sort Sheng, Xia
collection PubMed
description Activation of endoplasmic reticulum (ER) stress/the unfolded protein response (UPR) has been linked to cancer, but the molecular mechanisms are poorly understood and there is a paucity of reagents to translate this for cancer therapy. Here, we report that an IRE1α RNase-specific inhibitor, MKC8866, strongly inhibits prostate cancer (PCa) tumor growth as monotherapy in multiple preclinical models in mice and shows synergistic antitumor effects with current PCa drugs. Interestingly, global transcriptomic analysis reveal that IRE1α-XBP1s pathway activity is required for c-MYC signaling, one of the most highly activated oncogenic pathways in PCa. XBP1s is necessary for optimal c-MYC mRNA and protein expression, establishing, for the first time, a direct link between UPR and oncogene activation. In addition, an XBP1-specific gene expression signature is strongly associated with PCa prognosis. Our data establish IRE1α-XBP1s signaling as a central pathway in PCa and indicate that its targeting may offer novel treatment strategies.
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spelling pubmed-63459732019-01-28 IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling Sheng, Xia Nenseth, Hatice Zeynep Qu, Su Kuzu, Omer F. Frahnow, Turid Simon, Lukas Greene, Stephanie Zeng, Qingping Fazli, Ladan Rennie, Paul S. Mills, Ian G. Danielsen, Håvard Theis, Fabian Patterson, John B. Jin, Yang Saatcioglu, Fahri Nat Commun Article Activation of endoplasmic reticulum (ER) stress/the unfolded protein response (UPR) has been linked to cancer, but the molecular mechanisms are poorly understood and there is a paucity of reagents to translate this for cancer therapy. Here, we report that an IRE1α RNase-specific inhibitor, MKC8866, strongly inhibits prostate cancer (PCa) tumor growth as monotherapy in multiple preclinical models in mice and shows synergistic antitumor effects with current PCa drugs. Interestingly, global transcriptomic analysis reveal that IRE1α-XBP1s pathway activity is required for c-MYC signaling, one of the most highly activated oncogenic pathways in PCa. XBP1s is necessary for optimal c-MYC mRNA and protein expression, establishing, for the first time, a direct link between UPR and oncogene activation. In addition, an XBP1-specific gene expression signature is strongly associated with PCa prognosis. Our data establish IRE1α-XBP1s signaling as a central pathway in PCa and indicate that its targeting may offer novel treatment strategies. Nature Publishing Group UK 2019-01-24 /pmc/articles/PMC6345973/ /pubmed/30679434 http://dx.doi.org/10.1038/s41467-018-08152-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sheng, Xia
Nenseth, Hatice Zeynep
Qu, Su
Kuzu, Omer F.
Frahnow, Turid
Simon, Lukas
Greene, Stephanie
Zeng, Qingping
Fazli, Ladan
Rennie, Paul S.
Mills, Ian G.
Danielsen, Håvard
Theis, Fabian
Patterson, John B.
Jin, Yang
Saatcioglu, Fahri
IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling
title IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling
title_full IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling
title_fullStr IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling
title_full_unstemmed IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling
title_short IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling
title_sort ire1α-xbp1s pathway promotes prostate cancer by activating c-myc signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345973/
https://www.ncbi.nlm.nih.gov/pubmed/30679434
http://dx.doi.org/10.1038/s41467-018-08152-3
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