eEF2K—a new target in breast cancers with combined inactivation of p53 and PTEN

Abstract Extensive efforts have now characterized the somatic molecular alterations in human breast cancer (Cancer Genome Atlas Network, 2012; Stephens et al, 2012) and have led to a re‐definition of the disease as a constellation of 10 distinct driver‐based subtypes (IntClust subtypes) (Curtis et a...

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Main Authors: Hege G Russnes, Carlos Caldas
Format: Article
Language:English
Published: Springer Nature 2014-12-01
Series:EMBO Molecular Medicine
Online Access:https://doi.org/10.15252/emmm.201404683
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author Hege G Russnes
Carlos Caldas
author_facet Hege G Russnes
Carlos Caldas
author_sort Hege G Russnes
collection DOAJ
description Abstract Extensive efforts have now characterized the somatic molecular alterations in human breast cancer (Cancer Genome Atlas Network, 2012; Stephens et al, 2012) and have led to a re‐definition of the disease as a constellation of 10 distinct driver‐based subtypes (IntClust subtypes) (Curtis et al, 2012). The pursuit of druggable targets for each of these subtypes is now pressing. This is elegantly illustrated by the work of Liu et al (2014).
format Article
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institution Kabale University
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1757-4684
language English
publishDate 2014-12-01
publisher Springer Nature
record_format Article
series EMBO Molecular Medicine
spelling doaj-art-66a7a1f98438416da8cd9951d9d83c4f2025-08-20T03:43:01ZengSpringer NatureEMBO Molecular Medicine1757-46761757-46842014-12-016121512151410.15252/emmm.201404683eEF2K—a new target in breast cancers with combined inactivation of p53 and PTENHege G Russnes0Carlos Caldas1Department of Genetics, Institute for Cancer Research and Department of Pathology, Oslo University HospitalCancer Research UK Cambridge Institute and Department of Oncology, Li Ka Shing Centre, University of CambridgeAbstract Extensive efforts have now characterized the somatic molecular alterations in human breast cancer (Cancer Genome Atlas Network, 2012; Stephens et al, 2012) and have led to a re‐definition of the disease as a constellation of 10 distinct driver‐based subtypes (IntClust subtypes) (Curtis et al, 2012). The pursuit of druggable targets for each of these subtypes is now pressing. This is elegantly illustrated by the work of Liu et al (2014).https://doi.org/10.15252/emmm.201404683
spellingShingle Hege G Russnes
Carlos Caldas
eEF2K—a new target in breast cancers with combined inactivation of p53 and PTEN
EMBO Molecular Medicine
title eEF2K—a new target in breast cancers with combined inactivation of p53 and PTEN
title_full eEF2K—a new target in breast cancers with combined inactivation of p53 and PTEN
title_fullStr eEF2K—a new target in breast cancers with combined inactivation of p53 and PTEN
title_full_unstemmed eEF2K—a new target in breast cancers with combined inactivation of p53 and PTEN
title_short eEF2K—a new target in breast cancers with combined inactivation of p53 and PTEN
title_sort eef2k a new target in breast cancers with combined inactivation of p53 and pten
url https://doi.org/10.15252/emmm.201404683
work_keys_str_mv AT hegegrussnes eef2kanewtargetinbreastcancerswithcombinedinactivationofp53andpten
AT carloscaldas eef2kanewtargetinbreastcancerswithcombinedinactivationofp53andpten