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

ER stress and UPR are implicated in various cancers. Here, the authors show that one of the canonical UPR pathways, IRE1α-XBP1 regulates c-MYC signaling to promote prostate tumorigenesis, and pharmacological inhibition of IRE1α with MKC8866 inhibits prostate cancer growth and synergizes with clinica...

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Autores principales: Xia Sheng, Hatice Zeynep Nenseth, Su Qu, Omer F. Kuzu, Turid Frahnow, Lukas Simon, Stephanie Greene, Qingping Zeng, Ladan Fazli, Paul S. Rennie, Ian G. Mills, Håvard Danielsen, Fabian Theis, John B. Patterson, Yang Jin, Fahri Saatcioglu
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Lenguaje:EN
Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/9ced43e64be24399a78c2bfb98856c69
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spelling oai:doaj.org-article:9ced43e64be24399a78c2bfb98856c692021-12-02T15:35:12ZIRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling10.1038/s41467-018-08152-32041-1723https://doaj.org/article/9ced43e64be24399a78c2bfb98856c692019-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-08152-3https://doaj.org/toc/2041-1723ER stress and UPR are implicated in various cancers. Here, the authors show that one of the canonical UPR pathways, IRE1α-XBP1 regulates c-MYC signaling to promote prostate tumorigenesis, and pharmacological inhibition of IRE1α with MKC8866 inhibits prostate cancer growth and synergizes with clinically used prostate cancer drugs.Xia ShengHatice Zeynep NensethSu QuOmer F. KuzuTurid FrahnowLukas SimonStephanie GreeneQingping ZengLadan FazliPaul S. RennieIan G. MillsHåvard DanielsenFabian TheisJohn B. PattersonYang JinFahri SaatciogluNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Xia Sheng
Hatice Zeynep Nenseth
Su Qu
Omer F. Kuzu
Turid Frahnow
Lukas Simon
Stephanie Greene
Qingping Zeng
Ladan Fazli
Paul S. Rennie
Ian G. Mills
Håvard Danielsen
Fabian Theis
John B. Patterson
Yang Jin
Fahri Saatcioglu
IRE1α-XBP1s pathway promotes prostate cancer by activating c-MYC signaling
description ER stress and UPR are implicated in various cancers. Here, the authors show that one of the canonical UPR pathways, IRE1α-XBP1 regulates c-MYC signaling to promote prostate tumorigenesis, and pharmacological inhibition of IRE1α with MKC8866 inhibits prostate cancer growth and synergizes with clinically used prostate cancer drugs.
format article
author Xia Sheng
Hatice Zeynep Nenseth
Su Qu
Omer F. Kuzu
Turid Frahnow
Lukas Simon
Stephanie Greene
Qingping Zeng
Ladan Fazli
Paul S. Rennie
Ian G. Mills
Håvard Danielsen
Fabian Theis
John B. Patterson
Yang Jin
Fahri Saatcioglu
author_facet Xia Sheng
Hatice Zeynep Nenseth
Su Qu
Omer F. Kuzu
Turid Frahnow
Lukas Simon
Stephanie Greene
Qingping Zeng
Ladan Fazli
Paul S. Rennie
Ian G. Mills
Håvard Danielsen
Fabian Theis
John B. Patterson
Yang Jin
Fahri Saatcioglu
author_sort Xia Sheng
title 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_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_sort ire1α-xbp1s pathway promotes prostate cancer by activating c-myc signaling
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/9ced43e64be24399a78c2bfb98856c69
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