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PMID: 17483436 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, U.S. Gov't, Non-P.H.S.

MicroRNA expression profiles for the NCI-60 cancer cell panel.

Molecular cancer therapeutics ·Vol. 6 ·No. 5 ·2007-05-00 ·Pages 1483-91

Blower PE, Verducci JS, Lin S, Zhou J, Chung JH, Dai Z, Liu CG, Reinhold W, Lorenzi PL, Kaldjian EP, Croce CM, Weinstein JN, Sadee W

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.

MeSH Terms
Cell Line, Tumor Chromosome Aberrations Cluster Analysis DNA Mutational Analysis Drug Resistance, Neoplasm Drug Screening Assays, Antitumor/methods Gene Expression Regulation, Neoplastic Humans MicroRNAs Neoplasms/drug therapy,genetics,metabolism RNA, Messenger/metabolism
Chemicals
MicroRNAs RNA, Messenger
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Blower Paul E
Program of Pharmacogenomics, Department of Pharmacology and the Comprehensive Cancer Center, College of Medicine, The Ohio State University, 5072 Graves Hall, 333 West 10th Avenue, Columbus, OH 43210, USA. blower.7@osu.edu
Verducci Joseph S
Lin Shili
Zhou Jin
Chung Ji-Hyun
Dai Zunyan
Liu Chang-Gong
Reinhold William
Lorenzi Philip L
Kaldjian Eric P
Croce Carlo M
Weinstein John N
Sadee Wolfgang
Article Info
Journal
Molecular cancer therapeutics
Abbr.
Mol Cancer Ther
ISSN
1535-7163
Published
2007-05-00
Epub
2007-00-04
Pages
1483-91
Language
English
Region
United States
NLM ID
101132535
Subset
IM
Grants
NIGMS NIH HHS · GM61390 · United States
Intramural NIH HHS · United States
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