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Expression of MicroRNAs in the NCI-60 Cancer Cell-Lines

The NCI-60 panel of 60 human cancer cell-lines of nine different tissues of origin has been extensively characterized in biological, molecular and pharmacological studies. Analyses of data from such studies have provided valuable information for understanding cellular processes and developing strate...

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Autores principales: Patnaik, Santosh K., Dahlgaard, Jesper, Mazin, Wiktor, Kannisto, Eric, Jensen, Thomas, Knudsen, Steen, Yendamuri, Sai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509128/
https://www.ncbi.nlm.nih.gov/pubmed/23209617
http://dx.doi.org/10.1371/journal.pone.0049918
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author Patnaik, Santosh K.
Dahlgaard, Jesper
Mazin, Wiktor
Kannisto, Eric
Jensen, Thomas
Knudsen, Steen
Yendamuri, Sai
author_facet Patnaik, Santosh K.
Dahlgaard, Jesper
Mazin, Wiktor
Kannisto, Eric
Jensen, Thomas
Knudsen, Steen
Yendamuri, Sai
author_sort Patnaik, Santosh K.
collection PubMed
description The NCI-60 panel of 60 human cancer cell-lines of nine different tissues of origin has been extensively characterized in biological, molecular and pharmacological studies. Analyses of data from such studies have provided valuable information for understanding cellular processes and developing strategies for the diagnosis and treatment of cancer. Here, Affymetrix® GeneChip™ miRNA version 1 oligonucleotide microarrays were used to quantify 847 microRNAs to generate an expression dataset of 495 (58.4%) microRNAs that were identified as expressed in at least one cell-line of the NCI-60 panel. Accuracy of the microRNA measurements was partly confirmed by reverse transcription and polymerase chain reaction assays. Similar to that seen among the four existing NCI-60 microRNA datasets, the concordance of the new expression dataset with the other four was modest, with mean Pearson correlation coefficients of 0.37–0.54. In spite of this, comparable results with different datasets were noted in clustering of the cell-lines by their microRNA expression, differential expression of microRNAs by the lines’ tissue of origin, and correlation of specific microRNAs with the doubling-time of cells or their radiation sensitivity. Mutation status of the cell-lines for the TP53, PTEN and BRAF but not CDKN2A or KRAS cancer-related genes was found to be associated with changes in expression of specific microRNAs. The microRNA dataset generated here should be valuable to those working in the field of microRNAs as well as in integromic studies of the NCI-60 panel.
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spelling pubmed-35091282012-12-03 Expression of MicroRNAs in the NCI-60 Cancer Cell-Lines Patnaik, Santosh K. Dahlgaard, Jesper Mazin, Wiktor Kannisto, Eric Jensen, Thomas Knudsen, Steen Yendamuri, Sai PLoS One Research Article The NCI-60 panel of 60 human cancer cell-lines of nine different tissues of origin has been extensively characterized in biological, molecular and pharmacological studies. Analyses of data from such studies have provided valuable information for understanding cellular processes and developing strategies for the diagnosis and treatment of cancer. Here, Affymetrix® GeneChip™ miRNA version 1 oligonucleotide microarrays were used to quantify 847 microRNAs to generate an expression dataset of 495 (58.4%) microRNAs that were identified as expressed in at least one cell-line of the NCI-60 panel. Accuracy of the microRNA measurements was partly confirmed by reverse transcription and polymerase chain reaction assays. Similar to that seen among the four existing NCI-60 microRNA datasets, the concordance of the new expression dataset with the other four was modest, with mean Pearson correlation coefficients of 0.37–0.54. In spite of this, comparable results with different datasets were noted in clustering of the cell-lines by their microRNA expression, differential expression of microRNAs by the lines’ tissue of origin, and correlation of specific microRNAs with the doubling-time of cells or their radiation sensitivity. Mutation status of the cell-lines for the TP53, PTEN and BRAF but not CDKN2A or KRAS cancer-related genes was found to be associated with changes in expression of specific microRNAs. The microRNA dataset generated here should be valuable to those working in the field of microRNAs as well as in integromic studies of the NCI-60 panel. Public Library of Science 2012-11-28 /pmc/articles/PMC3509128/ /pubmed/23209617 http://dx.doi.org/10.1371/journal.pone.0049918 Text en © 2012 Patnaik et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Patnaik, Santosh K.
Dahlgaard, Jesper
Mazin, Wiktor
Kannisto, Eric
Jensen, Thomas
Knudsen, Steen
Yendamuri, Sai
Expression of MicroRNAs in the NCI-60 Cancer Cell-Lines
title Expression of MicroRNAs in the NCI-60 Cancer Cell-Lines
title_full Expression of MicroRNAs in the NCI-60 Cancer Cell-Lines
title_fullStr Expression of MicroRNAs in the NCI-60 Cancer Cell-Lines
title_full_unstemmed Expression of MicroRNAs in the NCI-60 Cancer Cell-Lines
title_short Expression of MicroRNAs in the NCI-60 Cancer Cell-Lines
title_sort expression of micrornas in the nci-60 cancer cell-lines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509128/
https://www.ncbi.nlm.nih.gov/pubmed/23209617
http://dx.doi.org/10.1371/journal.pone.0049918
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