Source:http://linkedlifedata.com/resource/pubmed/id/20335537
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
15
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pubmed:dateCreated |
2010-4-14
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pubmed:abstractText |
The hallmark of human cancer is heterogeneity, reflecting the complexity and variability of the vast array of somatic mutations acquired during oncogenesis. An ability to dissect this heterogeneity, to identify subgroups that represent common mechanisms of disease, will be critical to understanding the complexities of genetic alterations and to provide a framework to develop rational therapeutic strategies. Here, we describe a classification scheme for human breast cancer making use of patterns of pathway activity to build on previous subtype characterizations using intrinsic gene expression signatures, to provide a functional interpretation of the gene expression data that can be linked to therapeutic options. We show that the identified subgroups provide a robust mechanism for classifying independent samples, identifying tumors that share patterns of pathway activity and exhibit similar clinical and biological properties, including distinct patterns of chromosomal alterations that were not evident in the heterogeneous total population of tumors. We propose that this classification scheme provides a basis for understanding the complex mechanisms of oncogenesis that give rise to these tumors and to identify rational opportunities for combination therapies.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/5-RO1-CA106520-05,
http://linkedlifedata.com/resource/pubmed/grant/5-U54-CA112952-05,
http://linkedlifedata.com/resource/pubmed/grant/CA139890-01,
http://linkedlifedata.com/resource/pubmed/grant/HL007101-32,
http://linkedlifedata.com/resource/pubmed/grant/R01 CA106520-07
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1091-6490
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pubmed:author |
pubmed-author:BarryWilliam TWT,
pubmed-author:CrawfordMatthew DMD,
pubmed-author:DattoMichael BMB,
pubmed-author:GatzaMichael LML,
pubmed-author:KelleyMichaelM,
pubmed-author:KimJong WookJW,
pubmed-author:LucasJoseph EJE,
pubmed-author:Mathey-PrevotBernardB,
pubmed-author:NevinsJoseph RJR,
pubmed-author:PottiAnilA,
pubmed-author:WangQuanliQ
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pubmed:issnType |
Electronic
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pubmed:day |
13
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pubmed:volume |
107
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6994-9
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pubmed:dateRevised |
2010-12-3
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pubmed:meshHeading |
pubmed-meshheading:20335537-Algorithms,
pubmed-meshheading:20335537-Breast Neoplasms,
pubmed-meshheading:20335537-Cell Line, Tumor,
pubmed-meshheading:20335537-Cluster Analysis,
pubmed-meshheading:20335537-DNA,
pubmed-meshheading:20335537-Gene Dosage,
pubmed-meshheading:20335537-Gene Expression Profiling,
pubmed-meshheading:20335537-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:20335537-Genomics,
pubmed-meshheading:20335537-Humans,
pubmed-meshheading:20335537-Models, Genetic,
pubmed-meshheading:20335537-Nucleic Acid Hybridization,
pubmed-meshheading:20335537-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:20335537-Oligonucleotide Probes,
pubmed-meshheading:20335537-Phenotype
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pubmed:year |
2010
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pubmed:articleTitle |
A pathway-based classification of human breast cancer.
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pubmed:affiliation |
Duke Institute for Genome Sciences and Policy, Duke University Medical Center, Durham, NC 27710, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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