SplicerAV: a tool for mining microarray expression data for changes in RNA processing.

dc.contributor.author

Robinson, Timothy J

dc.contributor.author

Dinan, Michaela A

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Dewhirst, Mark

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Garcia-Blanco, Mariano A

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Pearson, James L

dc.coverage.spatial

England

dc.date.accessioned

2011-06-21T17:27:56Z

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2010-02-25

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BACKGROUND: Over the past two decades more than fifty thousand unique clinical and biological samples have been assayed using the Affymetrix HG-U133 and HG-U95 GeneChip microarray platforms. This substantial repository has been used extensively to characterize changes in gene expression between biological samples, but has not been previously mined en masse for changes in mRNA processing. We explored the possibility of using HG-U133 microarray data to identify changes in alternative mRNA processing in several available archival datasets. RESULTS: Data from these and other gene expression microarrays can now be mined for changes in transcript isoform abundance using a program described here, SplicerAV. Using in vivo and in vitro breast cancer microarray datasets, SplicerAV was able to perform both gene and isoform specific expression profiling within the same microarray dataset. Our reanalysis of Affymetrix U133 plus 2.0 data generated by in vitro over-expression of HRAS, E2F3, beta-catenin (CTNNB1), SRC, and MYC identified several hundred oncogene-induced mRNA isoform changes, one of which recognized a previously unknown mechanism of EGFR family activation. Using clinical data, SplicerAV predicted 241 isoform changes between low and high grade breast tumors; with changes enriched among genes coding for guanyl-nucleotide exchange factors, metalloprotease inhibitors, and mRNA processing factors. Isoform changes in 15 genes were associated with aggressive cancer across the three breast cancer datasets. CONCLUSIONS: Using SplicerAV, we identified several hundred previously uncharacterized isoform changes induced by in vitro oncogene over-expression and revealed a previously unknown mechanism of EGFR activation in human mammary epithelial cells. We analyzed Affymetrix GeneChip data from over 400 human breast tumors in three independent studies, making this the largest clinical dataset analyzed for en masse changes in alternative mRNA processing. The capacity to detect RNA isoform changes in archival microarray data using SplicerAV allowed us to carry out the first analysis of isoform specific mRNA changes directly associated with cancer survival.

dc.description.version

Version of Record

dc.identifier

http://www.ncbi.nlm.nih.gov/pubmed/20184770

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1471-2105-11-108

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1471-2105

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https://hdl.handle.net/10161/4332

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eng

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en_US

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Springer Science and Business Media LLC

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BMC Bioinformatics

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10.1186/1471-2105-11-108

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Bmc Bioinformatics

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Algorithms

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Biomarkers, Tumor

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Data Mining

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Databases, Genetic

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Gene Expression Profiling

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Neoplasms

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Oligonucleotide Array Sequence Analysis

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Protein Isoforms

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RNA, Messenger

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Software

dc.title

SplicerAV: a tool for mining microarray expression data for changes in RNA processing.

dc.title.alternative
dc.type

Journal article

duke.contributor.orcid

Dewhirst, Mark|0000-0003-3459-6546

duke.date.pubdate

2010-2-25

duke.description.issue
duke.description.volume

11

pubs.author-url

http://www.ncbi.nlm.nih.gov/pubmed/20184770

pubs.begin-page

108

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Basic Science Departments

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Biomedical Engineering

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Clinical Science Departments

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Duke

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Duke Cancer Institute

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Duke Clinical Research Institute

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Institutes and Centers

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Medicine

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Medicine, Medical Oncology

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Molecular Genetics and Microbiology

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Pathology

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Pratt School of Engineering

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Radiation Oncology

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School of Medicine

pubs.publication-status

Published online

pubs.volume

11

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