Context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancer

<p>Abstract</p> <p>Background</p> <p>Breast cancer is a highly heterogeneous disease with respect to molecular alterations and cellular composition making therapeutic and clinical outcome unpredictable. This diversity creates a significant challenge in developing tumor...

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Main Authors: Black Michael A, Cunliffe Heather E, Nasser Sara, Kim Seungchan
Format: Article
Language:English
Published: BMC 2011-03-01
Series:BMC Bioinformatics
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spelling doaj-7d29adaf0010410b834d4e95bc9faf2a2020-11-24T21:48:19ZengBMCBMC Bioinformatics1471-21052011-03-0112Suppl 2S310.1186/1471-2105-12-S2-S3Context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancerBlack Michael ACunliffe Heather ENasser SaraKim Seungchan<p>Abstract</p> <p>Background</p> <p>Breast cancer is a highly heterogeneous disease with respect to molecular alterations and cellular composition making therapeutic and clinical outcome unpredictable. This diversity creates a significant challenge in developing tumor classifications that are clinically reliable with respect to prognosis prediction.</p> <p>Results</p> <p>This paper describes an unsupervised context analysis to infer context-specific gene regulatory networks from 1,614 samples obtained from publicly available gene expression data, an extension of a previously published methodology. We use the context-specific gene regulatory networks to classify the tumors into clinically relevant subgroups, and provide candidates for a finer sub-grouping of the previously known intrinsic tumors with a focus on Basal-like tumors. Our analysis of pathway enrichment in the key contexts provides an insight into the biological mechanism underlying the identified subtypes of breast cancer.</p> <p>Conclusions</p> <p>The use of context-specific gene regulatory networks to identify biological contexts from heterogenous breast cancer data set was able to identify genomic drivers for subgroups within the previously reported intrinsic subtypes. These subgroups (contexts) uphold the clinical relevant features for the intrinsic subtypes and were associated with increased survival differences compared to the intrinsic subtypes. We believe our computational approach led to the generation of novel rationalized hypotheses to explain mechanisms of disease progression within sub-contexts of breast cancer that could be therapeutically exploited once validated.</p>
collection DOAJ
language English
format Article
sources DOAJ
author Black Michael A
Cunliffe Heather E
Nasser Sara
Kim Seungchan
spellingShingle Black Michael A
Cunliffe Heather E
Nasser Sara
Kim Seungchan
Context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancer
BMC Bioinformatics
author_facet Black Michael A
Cunliffe Heather E
Nasser Sara
Kim Seungchan
author_sort Black Michael A
title Context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancer
title_short Context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancer
title_full Context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancer
title_fullStr Context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancer
title_full_unstemmed Context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancer
title_sort context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancer
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2011-03-01
description <p>Abstract</p> <p>Background</p> <p>Breast cancer is a highly heterogeneous disease with respect to molecular alterations and cellular composition making therapeutic and clinical outcome unpredictable. This diversity creates a significant challenge in developing tumor classifications that are clinically reliable with respect to prognosis prediction.</p> <p>Results</p> <p>This paper describes an unsupervised context analysis to infer context-specific gene regulatory networks from 1,614 samples obtained from publicly available gene expression data, an extension of a previously published methodology. We use the context-specific gene regulatory networks to classify the tumors into clinically relevant subgroups, and provide candidates for a finer sub-grouping of the previously known intrinsic tumors with a focus on Basal-like tumors. Our analysis of pathway enrichment in the key contexts provides an insight into the biological mechanism underlying the identified subtypes of breast cancer.</p> <p>Conclusions</p> <p>The use of context-specific gene regulatory networks to identify biological contexts from heterogenous breast cancer data set was able to identify genomic drivers for subgroups within the previously reported intrinsic subtypes. These subgroups (contexts) uphold the clinical relevant features for the intrinsic subtypes and were associated with increased survival differences compared to the intrinsic subtypes. We believe our computational approach led to the generation of novel rationalized hypotheses to explain mechanisms of disease progression within sub-contexts of breast cancer that could be therapeutically exploited once validated.</p>
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