共 34 条
Characterization of the Melanoma miRNAome by Deep Sequencing
被引:167
作者:

Stark, Mitchell S.
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机构:
Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia

Tyagi, Sonika
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Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia

Nancarrow, Derek J.
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Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia

Boyle, Glen M.
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机构:
Queensland Inst Med Res, Drug Discovery Lab, Brisbane, Qld 4006, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia

Cook, Anthony L.
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机构:
Univ Queensland, Inst Mol Biosci, Melanogenix Grp, St Lucia, Qld, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia

Whiteman, David C.
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Queensland Inst Med Res, Canc Control Grp, Brisbane, Qld 4006, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia

Parsons, Peter G.
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Queensland Inst Med Res, Drug Discovery Lab, Brisbane, Qld 4006, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia

Schmidt, Christopher
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机构:
Queensland Inst Med Res, Canc Immunotherapy Grp, Brisbane, Qld 4006, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia

Sturm, Richard A.
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机构:
Univ Queensland, Inst Mol Biosci, Melanogenix Grp, St Lucia, Qld, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia

Hayward, Nicholas K.
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机构:
Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia
机构:
[1] Queensland Inst Med Res, Oncogenom Lab, Brisbane, Qld 4006, Australia
[2] Queensland Inst Med Res, Drug Discovery Lab, Brisbane, Qld 4006, Australia
[3] Queensland Inst Med Res, Canc Control Grp, Brisbane, Qld 4006, Australia
[4] Univ Queensland, Inst Mol Biosci, Melanogenix Grp, St Lucia, Qld, Australia
[5] Queensland Inst Med Res, Canc Immunotherapy Grp, Brisbane, Qld 4006, Australia
来源:
PLOS ONE
|
2010年
/
5卷
/
03期
基金:
英国医学研究理事会;
关键词:
CELL-PROLIFERATION;
TUMOR INVASION;
EXPRESSION;
MICRORNAS;
MELANOCYTES;
PROGRESSION;
METASTASIS;
REPRESSION;
REVEALS;
MARKER;
D O I:
10.1371/journal.pone.0009685
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Background: 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. Methodology/Principal Findings: 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. Conclusions/Significance: 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.
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