Characterization of the Melanoma miRNAome by Deep Sequencing.

<h4>Background</h4>MicroRNAs (miRNAs) are 18-23 nucleotide non-coding RNAs that regulate gene expression in a sequence specific manner. Little is known about the repertoire and function of miRNAs in melanoma or the melanocytic lineage. We therefore undertook a comprehensive analysis of t...

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Autores principales: Mitchell S Stark, Sonika Tyagi, Derek J Nancarrow, Glen M Boyle, Anthony L Cook, David C Whiteman, Peter G Parsons, Christopher Schmidt, Richard A Sturm, Nicholas K Hayward
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Publicado: Public Library of Science (PLoS) 2010
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Acceso en línea:https://doaj.org/article/d9667309fcd04ebd90a10cb95236c9b0
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spelling oai:doaj.org-article:d9667309fcd04ebd90a10cb95236c9b02021-11-25T06:25:29ZCharacterization of the Melanoma miRNAome by Deep Sequencing.1932-620310.1371/journal.pone.0009685https://doaj.org/article/d9667309fcd04ebd90a10cb95236c9b02010-03-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20300190/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>MicroRNAs (miRNAs) are 18-23 nucleotide non-coding RNAs that regulate gene expression in a sequence specific manner. Little is known about the repertoire and function of miRNAs in melanoma or the melanocytic lineage. We therefore undertook a comprehensive analysis of the miRNAome in a diverse range of pigment cells including: melanoblasts, melanocytes, congenital nevocytes, acral, mucosal, cutaneous and uveal melanoma cells.<h4>Methodology/principal findings</h4>We sequenced 12 small RNA libraries using Illumina's Genome Analyzer II platform. This massively parallel sequencing approach of a diverse set of melanoma and pigment cell libraries revealed a total of 539 known mature and mature-star sequences, along with the prediction of 279 novel miRNA candidates, of which 109 were common to 2 or more libraries and 3 were present in all libraries.<h4>Conclusions/significance</h4>Some of the novel candidate miRNAs may be specific to the melanocytic lineage and as such could be used as biomarkers to assist in the early detection of distant metastases by measuring the circulating levels in blood. Follow up studies of the functional roles of these pigment cell miRNAs and the identification of the targets should shed further light on the development and progression of melanoma.Mitchell S StarkSonika TyagiDerek J NancarrowGlen M BoyleAnthony L CookDavid C WhitemanPeter G ParsonsChristopher SchmidtRichard A SturmNicholas K HaywardPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 3, p e9685 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Mitchell S Stark
Sonika Tyagi
Derek J Nancarrow
Glen M Boyle
Anthony L Cook
David C Whiteman
Peter G Parsons
Christopher Schmidt
Richard A Sturm
Nicholas K Hayward
Characterization of the Melanoma miRNAome by Deep Sequencing.
description <h4>Background</h4>MicroRNAs (miRNAs) are 18-23 nucleotide non-coding RNAs that regulate gene expression in a sequence specific manner. Little is known about the repertoire and function of miRNAs in melanoma or the melanocytic lineage. We therefore undertook a comprehensive analysis of the miRNAome in a diverse range of pigment cells including: melanoblasts, melanocytes, congenital nevocytes, acral, mucosal, cutaneous and uveal melanoma cells.<h4>Methodology/principal findings</h4>We sequenced 12 small RNA libraries using Illumina's Genome Analyzer II platform. This massively parallel sequencing approach of a diverse set of melanoma and pigment cell libraries revealed a total of 539 known mature and mature-star sequences, along with the prediction of 279 novel miRNA candidates, of which 109 were common to 2 or more libraries and 3 were present in all libraries.<h4>Conclusions/significance</h4>Some of the novel candidate miRNAs may be specific to the melanocytic lineage and as such could be used as biomarkers to assist in the early detection of distant metastases by measuring the circulating levels in blood. Follow up studies of the functional roles of these pigment cell miRNAs and the identification of the targets should shed further light on the development and progression of melanoma.
format article
author Mitchell S Stark
Sonika Tyagi
Derek J Nancarrow
Glen M Boyle
Anthony L Cook
David C Whiteman
Peter G Parsons
Christopher Schmidt
Richard A Sturm
Nicholas K Hayward
author_facet Mitchell S Stark
Sonika Tyagi
Derek J Nancarrow
Glen M Boyle
Anthony L Cook
David C Whiteman
Peter G Parsons
Christopher Schmidt
Richard A Sturm
Nicholas K Hayward
author_sort Mitchell S Stark
title Characterization of the Melanoma miRNAome by Deep Sequencing.
title_short Characterization of the Melanoma miRNAome by Deep Sequencing.
title_full Characterization of the Melanoma miRNAome by Deep Sequencing.
title_fullStr Characterization of the Melanoma miRNAome by Deep Sequencing.
title_full_unstemmed Characterization of the Melanoma miRNAome by Deep Sequencing.
title_sort characterization of the melanoma mirnaome by deep sequencing.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/d9667309fcd04ebd90a10cb95236c9b0
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