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The Prognostic and Predictive Value of Melanoma-related MicroRNAs Using Tissue and Serum: A MicroRNA Expression Analysis.

Authors :
Stark MS
Klein K
Weide B
Haydu LE
Pflugfelder A
Tang YH
Palmer JM
Whiteman DC
Scolyer RA
Mann GJ
Thompson JF
Long GV
Barbour AP
Soyer HP
Garbe C
Herington A
Pollock PM
Hayward NK
Source :
EBioMedicine [EBioMedicine] 2015 May 12; Vol. 2 (7), pp. 671-80. Date of Electronic Publication: 2015 May 12 (Print Publication: 2015).
Publication Year :
2015

Abstract

The overall 5-year survival for melanoma is 91%. However, if distant metastasis occurs (stage IV), cure rates are < 15%. Hence, melanoma detection in earlier stages (stages I-III) maximises the chances of patient survival. We measured the expression of a panel of 17 microRNAs (miRNAs) (MELmiR-17) in melanoma tissues (stage III; n = 76 and IV; n = 10) and serum samples (collected from controls with no melanoma, n = 130; and patients with melanoma (stages I/II, n = 86; III, n = 50; and IV, n = 119)) obtained from biobanks in Australia and Germany. In melanoma tissues, members of the 'MELmiR-17' panel were found to be predictors of stage, recurrence, and survival. Additionally, in a minimally-invasive blood test, a seven-miRNA panel (MELmiR-7) detected the presence of melanoma (relative to controls) with high sensitivity (93%) and specificity (≥ 82%) when ≥ 4 miRNAs were expressed. Moreover, the 'MELmiR-7' panel characterised overall survival of melanoma patients better than both serum LDH and S100B (delta log likelihood = 11, p < 0.001). This panel was found to be superior to currently used serological markers for melanoma progression, recurrence, and survival; and would be ideally suited to monitor tumour progression in patients diagnosed with early metastatic disease (stages IIIa-c/IV M1a-b) to detect relapse following surgical or adjuvant treatment.

Details

Language :
English
ISSN :
2352-3964
Volume :
2
Issue :
7
Database :
MEDLINE
Journal :
EBioMedicine
Publication Type :
Academic Journal
Accession number :
26288839
Full Text :
https://doi.org/10.1016/j.ebiom.2015.05.011