EBioMedicine (Jul 2015)

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

  • Mitchell S. Stark,
  • Kerenaftali Klein,
  • Benjamin Weide,
  • Lauren E. Haydu,
  • Annette Pflugfelder,
  • Yue Hang Tang,
  • Jane M. Palmer,
  • David C. Whiteman,
  • Richard A. Scolyer,
  • Graham J. Mann,
  • John F. Thompson,
  • Georgina V. Long,
  • Andrew P. Barbour,
  • H. Peter Soyer,
  • Claus Garbe,
  • Adrian Herington,
  • Pamela M. Pollock,
  • Nicholas K. Hayward

DOI
https://doi.org/10.1016/j.ebiom.2015.05.011
Journal volume & issue
Vol. 2, no. 7
pp. 671 – 680

Abstract

Read online

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.

Keywords