Dual functions of SPOP and ERG dictate androgen therapy responses in prostate cancer

Gene fusions involving the ERG transcription factor and point mutations in the ubiquitin ligase adaptor SPOP are two truncal mutations that are mutually exclusively present in prostate cancer. Here, the authors show that mutations in SPOP render prostate tumor cells sensitive to antiandrogen therapy...

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Main Authors: Tiziano Bernasocchi, Geniver El Tekle, Marco Bolis, Azzurra Mutti, Arianna Vallerga, Laura P. Brandt, Filippo Spriano, Tanya Svinkina, Marita Zoma, Valentina Ceserani, Anna Rinaldi, Hana Janouskova, Daniela Bossi, Manuela Cavalli, Simone Mosole, Roger Geiger, Ze Dong, Cai-Guang Yang, Domenico Albino, Andrea Rinaldi, Peter Schraml, Simon Linder, Giuseppina M. Carbone, Andrea Alimonti, Francesco Bertoni, Holger Moch, Steven A. Carr, Wilbert Zwart, Marianna Kruithof-de Julio, Mark A. Rubin, Namrata D. Udeshi, Jean-Philippe P. Theurillat
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-020-20820-x
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spelling doaj-f2c4c2cbe140413794b564af2e6c87752021-02-07T12:13:40ZengNature Publishing GroupNature Communications2041-17232021-02-0112111810.1038/s41467-020-20820-xDual functions of SPOP and ERG dictate androgen therapy responses in prostate cancerTiziano Bernasocchi0Geniver El Tekle1Marco Bolis2Azzurra Mutti3Arianna Vallerga4Laura P. Brandt5Filippo Spriano6Tanya Svinkina7Marita Zoma8Valentina Ceserani9Anna Rinaldi10Hana Janouskova11Daniela Bossi12Manuela Cavalli13Simone Mosole14Roger Geiger15Ze Dong16Cai-Guang Yang17Domenico Albino18Andrea Rinaldi19Peter Schraml20Simon Linder21Giuseppina M. Carbone22Andrea Alimonti23Francesco Bertoni24Holger Moch25Steven A. Carr26Wilbert Zwart27Marianna Kruithof-de Julio28Mark A. Rubin29Namrata D. Udeshi30Jean-Philippe P. Theurillat31Institute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaDepartment of Biomedical Research, University of BernInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaThe Broad Institute of MIT & HarvardInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute for Research in BiomedicineState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of SciencesState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of SciencesInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaDepartment of Pathology and Molecular Pathology, University Hospital ZurichThe Netherlands Cancer Institute, Oncode InstituteInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaDepartment of Pathology and Molecular Pathology, University Hospital ZurichThe Broad Institute of MIT & HarvardThe Netherlands Cancer Institute, Oncode InstituteDepartment of Biomedical Research, Urology Research Laboratory, University of BernDepartment of Biomedical Research, University of BernThe Broad Institute of MIT & HarvardInstitute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italianaGene fusions involving the ERG transcription factor and point mutations in the ubiquitin ligase adaptor SPOP are two truncal mutations that are mutually exclusively present in prostate cancer. Here, the authors show that mutations in SPOP render prostate tumor cells sensitive to antiandrogen therapy and that the presence of ERG promotes sensitivity to high dose of androgen and SPOP inhibition.https://doi.org/10.1038/s41467-020-20820-x
collection DOAJ
language English
format Article
sources DOAJ
author Tiziano Bernasocchi
Geniver El Tekle
Marco Bolis
Azzurra Mutti
Arianna Vallerga
Laura P. Brandt
Filippo Spriano
Tanya Svinkina
Marita Zoma
Valentina Ceserani
Anna Rinaldi
Hana Janouskova
Daniela Bossi
Manuela Cavalli
Simone Mosole
Roger Geiger
Ze Dong
Cai-Guang Yang
Domenico Albino
Andrea Rinaldi
Peter Schraml
Simon Linder
Giuseppina M. Carbone
Andrea Alimonti
Francesco Bertoni
Holger Moch
Steven A. Carr
Wilbert Zwart
Marianna Kruithof-de Julio
Mark A. Rubin
Namrata D. Udeshi
Jean-Philippe P. Theurillat
spellingShingle Tiziano Bernasocchi
Geniver El Tekle
Marco Bolis
Azzurra Mutti
Arianna Vallerga
Laura P. Brandt
Filippo Spriano
Tanya Svinkina
Marita Zoma
Valentina Ceserani
Anna Rinaldi
Hana Janouskova
Daniela Bossi
Manuela Cavalli
Simone Mosole
Roger Geiger
Ze Dong
Cai-Guang Yang
Domenico Albino
Andrea Rinaldi
Peter Schraml
Simon Linder
Giuseppina M. Carbone
Andrea Alimonti
Francesco Bertoni
Holger Moch
Steven A. Carr
Wilbert Zwart
Marianna Kruithof-de Julio
Mark A. Rubin
Namrata D. Udeshi
Jean-Philippe P. Theurillat
Dual functions of SPOP and ERG dictate androgen therapy responses in prostate cancer
Nature Communications
author_facet Tiziano Bernasocchi
Geniver El Tekle
Marco Bolis
Azzurra Mutti
Arianna Vallerga
Laura P. Brandt
Filippo Spriano
Tanya Svinkina
Marita Zoma
Valentina Ceserani
Anna Rinaldi
Hana Janouskova
Daniela Bossi
Manuela Cavalli
Simone Mosole
Roger Geiger
Ze Dong
Cai-Guang Yang
Domenico Albino
Andrea Rinaldi
Peter Schraml
Simon Linder
Giuseppina M. Carbone
Andrea Alimonti
Francesco Bertoni
Holger Moch
Steven A. Carr
Wilbert Zwart
Marianna Kruithof-de Julio
Mark A. Rubin
Namrata D. Udeshi
Jean-Philippe P. Theurillat
author_sort Tiziano Bernasocchi
title Dual functions of SPOP and ERG dictate androgen therapy responses in prostate cancer
title_short Dual functions of SPOP and ERG dictate androgen therapy responses in prostate cancer
title_full Dual functions of SPOP and ERG dictate androgen therapy responses in prostate cancer
title_fullStr Dual functions of SPOP and ERG dictate androgen therapy responses in prostate cancer
title_full_unstemmed Dual functions of SPOP and ERG dictate androgen therapy responses in prostate cancer
title_sort dual functions of spop and erg dictate androgen therapy responses in prostate cancer
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2021-02-01
description Gene fusions involving the ERG transcription factor and point mutations in the ubiquitin ligase adaptor SPOP are two truncal mutations that are mutually exclusively present in prostate cancer. Here, the authors show that mutations in SPOP render prostate tumor cells sensitive to antiandrogen therapy and that the presence of ERG promotes sensitivity to high dose of androgen and SPOP inhibition.
url https://doi.org/10.1038/s41467-020-20820-x
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