Pharmacological induction of selective endoplasmic reticulum retention as a strategy for cancer therapy

Inhibition of PERK, an endoplasmic reticulum (ER) unfolded protein response (UPR) protein, is a potential pharmacological target for cancer treatment. Here, the authors show that inhibition of PERK under ER stress affects trafficking from the ER to the surface of several key receptor tyrosine kinase...

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Main Authors: Mohamed Mahameed, Shatha Boukeileh, Akram Obiedat, Odai Darawshi, Priya Dipta, Amit Rimon, Gordon McLennan, Rosi Fassler, Dana Reichmann, Rotem Karni, Christian Preisinger, Thomas Wilhelm, Michael Huber, Boaz Tirosh
Format: Article
Language:English
Published: Nature Portfolio 2020-03-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-020-15067-5
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author Mohamed Mahameed
Shatha Boukeileh
Akram Obiedat
Odai Darawshi
Priya Dipta
Amit Rimon
Gordon McLennan
Rosi Fassler
Dana Reichmann
Rotem Karni
Christian Preisinger
Thomas Wilhelm
Michael Huber
Boaz Tirosh
author_facet Mohamed Mahameed
Shatha Boukeileh
Akram Obiedat
Odai Darawshi
Priya Dipta
Amit Rimon
Gordon McLennan
Rosi Fassler
Dana Reichmann
Rotem Karni
Christian Preisinger
Thomas Wilhelm
Michael Huber
Boaz Tirosh
author_sort Mohamed Mahameed
collection DOAJ
description Inhibition of PERK, an endoplasmic reticulum (ER) unfolded protein response (UPR) protein, is a potential pharmacological target for cancer treatment. Here, the authors show that inhibition of PERK under ER stress affects trafficking from the ER to the surface of several key receptor tyrosine kinases, suggesting a selective ER retention.
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spelling doaj.art-41b3dd4a0c9748dc8d4f1d07443c6ee22022-12-21T23:38:51ZengNature PortfolioNature Communications2041-17232020-03-0111111410.1038/s41467-020-15067-5Pharmacological induction of selective endoplasmic reticulum retention as a strategy for cancer therapyMohamed Mahameed0Shatha Boukeileh1Akram Obiedat2Odai Darawshi3Priya Dipta4Amit Rimon5Gordon McLennan6Rosi Fassler7Dana Reichmann8Rotem Karni9Christian Preisinger10Thomas Wilhelm11Michael Huber12Boaz Tirosh13Institute for Drug Research, The Hebrew University of JerusalemInstitute for Drug Research, The Hebrew University of JerusalemInstitute for Drug Research, The Hebrew University of JerusalemInstitute for Drug Research, The Hebrew University of JerusalemInstitute for Drug Research, The Hebrew University of JerusalemInstitute for Drug Research, The Hebrew University of JerusalemLerner Research Institute, Cleveland Clinic FoundationThe Alexander Silberman Institute of Life Sciences, The Hebrew University of JerusalemThe Alexander Silberman Institute of Life Sciences, The Hebrew University of JerusalemDepartment of Biochemistry, Faculty of Medicine, IMRIC, The Hebrew University of JerusalemProteomics Facility, IZKF Aachen, RWTH Aachen UniversityInstitute of Biochemistry and Molecular Immunology, Medical School, RWTH Aachen UniversityInstitute of Biochemistry and Molecular Immunology, Medical School, RWTH Aachen UniversityInstitute for Drug Research, The Hebrew University of JerusalemInhibition of PERK, an endoplasmic reticulum (ER) unfolded protein response (UPR) protein, is a potential pharmacological target for cancer treatment. Here, the authors show that inhibition of PERK under ER stress affects trafficking from the ER to the surface of several key receptor tyrosine kinases, suggesting a selective ER retention.https://doi.org/10.1038/s41467-020-15067-5
spellingShingle Mohamed Mahameed
Shatha Boukeileh
Akram Obiedat
Odai Darawshi
Priya Dipta
Amit Rimon
Gordon McLennan
Rosi Fassler
Dana Reichmann
Rotem Karni
Christian Preisinger
Thomas Wilhelm
Michael Huber
Boaz Tirosh
Pharmacological induction of selective endoplasmic reticulum retention as a strategy for cancer therapy
Nature Communications
title Pharmacological induction of selective endoplasmic reticulum retention as a strategy for cancer therapy
title_full Pharmacological induction of selective endoplasmic reticulum retention as a strategy for cancer therapy
title_fullStr Pharmacological induction of selective endoplasmic reticulum retention as a strategy for cancer therapy
title_full_unstemmed Pharmacological induction of selective endoplasmic reticulum retention as a strategy for cancer therapy
title_short Pharmacological induction of selective endoplasmic reticulum retention as a strategy for cancer therapy
title_sort pharmacological induction of selective endoplasmic reticulum retention as a strategy for cancer therapy
url https://doi.org/10.1038/s41467-020-15067-5
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