ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancer

Despite initial benefits in treating HER2-positive breast cancer patients with lapatinib, resistance is prevalent. Here the authors show that lapatinib resistance can be ascribed to mTOR-mediated re-activation of ERRα and to the consequent induction of a metabolic adaptation.

Bibliographic Details
Main Authors: Geneviève Deblois, Harvey W. Smith, Ingrid S. Tam, Simon-Pierre Gravel, Maxime Caron, Paul Savage, David P. Labbé, Louis R. Bégin, Michel L. Tremblay, Morag Park, Guillaume Bourque, Julie St-Pierre, William J. Muller, Vincent Giguère
Format: Article
Language:English
Published: Nature Publishing Group 2016-07-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/ncomms12156
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spelling doaj-a807b71593d5451987bf6593688f61a32021-05-11T10:43:40ZengNature Publishing GroupNature Communications2041-17232016-07-017111410.1038/ncomms12156ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancerGeneviève Deblois0Harvey W. Smith1Ingrid S. Tam2Simon-Pierre Gravel3Maxime Caron4Paul Savage5David P. Labbé6Louis R. Bégin7Michel L. Tremblay8Morag Park9Guillaume Bourque10Julie St-Pierre11William J. Muller12Vincent Giguère13Goodman Cancer Research Centre, McGill UniversityGoodman Cancer Research Centre, McGill UniversityGoodman Cancer Research Centre, McGill UniversityGoodman Cancer Research Centre, McGill UniversityDepartment of Human Genetics, McGill UniversityGoodman Cancer Research Centre, McGill UniversityGoodman Cancer Research Centre, McGill UniversityService d’anatomopathologie, Hôpital du Sacré-Cœur de MontréalGoodman Cancer Research Centre, McGill UniversityGoodman Cancer Research Centre, McGill UniversityDepartment of Human Genetics, McGill UniversityGoodman Cancer Research Centre, McGill UniversityGoodman Cancer Research Centre, McGill UniversityGoodman Cancer Research Centre, McGill UniversityDespite initial benefits in treating HER2-positive breast cancer patients with lapatinib, resistance is prevalent. Here the authors show that lapatinib resistance can be ascribed to mTOR-mediated re-activation of ERRα and to the consequent induction of a metabolic adaptation.https://doi.org/10.1038/ncomms12156
collection DOAJ
language English
format Article
sources DOAJ
author Geneviève Deblois
Harvey W. Smith
Ingrid S. Tam
Simon-Pierre Gravel
Maxime Caron
Paul Savage
David P. Labbé
Louis R. Bégin
Michel L. Tremblay
Morag Park
Guillaume Bourque
Julie St-Pierre
William J. Muller
Vincent Giguère
spellingShingle Geneviève Deblois
Harvey W. Smith
Ingrid S. Tam
Simon-Pierre Gravel
Maxime Caron
Paul Savage
David P. Labbé
Louis R. Bégin
Michel L. Tremblay
Morag Park
Guillaume Bourque
Julie St-Pierre
William J. Muller
Vincent Giguère
ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancer
Nature Communications
author_facet Geneviève Deblois
Harvey W. Smith
Ingrid S. Tam
Simon-Pierre Gravel
Maxime Caron
Paul Savage
David P. Labbé
Louis R. Bégin
Michel L. Tremblay
Morag Park
Guillaume Bourque
Julie St-Pierre
William J. Muller
Vincent Giguère
author_sort Geneviève Deblois
title ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancer
title_short ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancer
title_full ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancer
title_fullStr ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancer
title_full_unstemmed ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancer
title_sort errα mediates metabolic adaptations driving lapatinib resistance in breast cancer
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2016-07-01
description Despite initial benefits in treating HER2-positive breast cancer patients with lapatinib, resistance is prevalent. Here the authors show that lapatinib resistance can be ascribed to mTOR-mediated re-activation of ERRα and to the consequent induction of a metabolic adaptation.
url https://doi.org/10.1038/ncomms12156
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