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Subtype and pathway specific responses to anticancer compounds in breast cancer

Authors :
Heidi S. Feiler
Eric A. Collisson
Joel Greshock
Mary Ann Hardwicke
Elizabeth Purdom
Gordon B. Mills
Bryan T. Hennessy
Lakshmi Jakkula
Pete Smith
Yinghui Guan
James E. Korkola
John W. Park
Joe W. Gray
Nicholas J. Wang
William J. Gibb
Kurtis E. Bachman
Denise M. Wolf
Lyubomir T. Vassilev
Henrik Bengtsson
Kenneth Wood
Stephen C. Benz
Zhi Hu
Anguraj Sadanandam
Nora Bayani
François Pepin
Frances Tong
Terence P. Speed
Laura M. Heiser
Sam Ng
Steffen Durinck
Theodore C. Goldstein
Joshua M. Stuart
Wen-Lin Kuo
Richard M. Neve
Paul T. Spellman
Jessica Billig
David Haussler
Sophia Lewis
Safiyyah Ziyad
Richard Wooster
Andrea Dueregger
Pierre Neuvial
Laurence J. Marton
Life Science Division [LBNL Berkeley]
Lawrence Berkeley National Laboratory [Berkeley] (LBNL)
Department of Biomolecular Engineering
University of California [Santa Cruz] (UCSC)
University of California-University of California
Center for Biomolecular Science and Engineering
Department of Statistics [Berkeley]
University of California [Berkeley]
Laboratoire Statistique et Génome (SG)
Institut National de la Recherche Agronomique (INRA)-Université d'Évry-Val-d'Essonne (UEVE)-Centre National de la Recherche Scientifique (CNRS)
Department of Epidemiology and Biostatistics, University of California, San Francisco
University of California [San Francisco] (UCSF)
Cytokinetics Inc
Oncology
Millenium Pharmaceuticals
Hoffmann-La Roche Ltd
Department of Systems Biology, The University of Texas MD Anderson Cancer Center
The University of Texas M.D. Anderson Cancer Center [Houston]
GlaxoSmithKline
Glaxo Smith Kline
Division of Hematology-Oncology
Progen Pharmaceuticals
The Walter and Eliza Hall Institute of Medical Research (WEHI)
The Walter and Eliza Hall Institute of Medical Research
Howard Hughes Medical Institute [Santa Cruz] (HHMI)
Center for Biomolecular Science & Engineering
Department of Computer Science [Alabama]
University of Alabama [Tuscaloosa] (UA)
University of California-University of California-Howard Hughes Medical Institute (HHMI)
University of California [Santa Cruz] (UC Santa Cruz)
University of California (UC)-University of California (UC)
University of California [Berkeley] (UC Berkeley)
University of California [San Francisco] (UC San Francisco)
F. Hoffmann-La Roche [Basel]
Howard Hughes Medical Institute (HHMI)-University of California [Santa Cruz] (UC Santa Cruz)
Source :
Proceedings of the National Academy of Sciences of the United States of America, Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2012, 109 (8), pp.2724-9, Proceedings of the National Academy of Sciences of the United States of America, 2012, 109 (8), pp.2724-9
Publication Year :
2012
Publisher :
HAL CCSD, 2012.

Abstract

International audience; Breast cancers are comprised of molecularly distinct subtypes that may respond differently to pathway-targeted therapies now under development. Collections of breast cancer cell lines mirror many of the molecular subtypes and pathways found in tumors, suggesting that treatment of cell lines with candidate therapeutic compounds can guide identification of associations between molecular subtypes, pathways, and drug response. In a test of 77 therapeutic compounds, nearly all drugs showed differential responses across these cell lines, and approximately one third showed subtype-, pathway-, and/or genomic aberration-specific responses. These observations suggest mechanisms of response and resistance and may inform efforts to develop molecular assays that predict clinical response.

Details

Language :
English
ISSN :
00278424 and 10916490
Database :
OpenAIRE
Journal :
Proceedings of the National Academy of Sciences of the United States of America, Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2012, 109 (8), pp.2724-9, Proceedings of the National Academy of Sciences of the United States of America, 2012, 109 (8), pp.2724-9
Accession number :
edsair.doi.dedup.....4bb2526104d8cc0a0b3717f7a4b21e64