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Published online first on May 4, 2007
[Molecular Cancer Therapeutics, 10.1158/1535-7163.MCT-07-0009]
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Research Articles: Therapeutics, Targets, and Development

MicroRNA expression profiles for the NCI-60 cancer cell p anel

Paul E. Blower 1*, Joseph S. Verducci , Shili Lin , Jin Zhou , Ji-Hyun Chung , Zunyan Dai , Chang-Gong Liu , William Reinhold , Philip L. Lorenzi , Eric P. Kaldjian , Carlo M. Croce , John N. Weinstein , Wolfgang Sadee

1 1Program of Pharmacogenomics, Department of Pharmacology and the Comprehensive Cancer Center, College of Medicine, Departments of 2Statistics, 3Mathematical Biosciences Institute, and 4Department of Molecular Virology, Immunology and Medical Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio; 5Genomics and Bioinformatics Group, Laboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland; 6GeneLogic, Inc., Gaithersburg, Maryland

* To whom correspondence should be addressed. E-mail: blower.7{at}osu.edu.


   Abstract

Advances in the understanding of cancer cell biology and response to drug treatment have benefited from new molecular technologies and methods for integrating information from multiple sources. The NCI-60, a panel of 60 diverse human cancer cell lines, has been used by the National Cancer Institute to screen >100,000 chemical compounds and natural product extracts for anticancer activity. The NCI-60 has also been profiled for mRNA and protein expression, mutational status, chromosomal aberrations, and DNA copy number, generating an unparalleled public resource for integrated chemogenomic studies. Recently, microRNAs have been shown to target particular sets of mRNAs, thereby preventing translation or accelerating mRNA turnover. To complement the existing NCI-60 data sets, we have measured expression levels of microRNAs in the NCI-60 and incorporated the resulting data into the CellMiner program package for integrative analysis. Cell line groupings based on microRNA expression were generally consistent with tissue type and with cell line clustering based on mRNA expression. However, mRNA expression seemed to be somewhat more informative for discriminating among tissue types than was microRNA expression. In addition, we found that there does not seem to be a significant correlation between microRNA expression patterns and those of known target transcripts. Comparison of microRNA expression patterns and compound potency patterns showed significant correlations, suggesting that microRNAs may play a role in chemoresistance. Combined with gene expression and other biological data using multivariate analysis, microRNA expression profiles may provide a critical link for understanding mechanisms involved in chemosensitivity and chemoresistance. [Mol Cancer Ther 2007;6(5):OF1-9]

Key Words: microRNA, microarray, NCI-60, clustering, correlation




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Copyright © 2007 by the American Association for Cancer Research.