MicroRNA-mediated regulation of melanoma

Br J Dermatol. 2014 Aug;171(2):234-41. doi: 10.1111/bjd.12989. Epub 2014 Jul 26.

Abstract

Melanoma is one of the most aggressive and deadly skin cancers, and, in its advanced stages, accounts for > 80% mortality. The incidence of melanoma is increasing worldwide; however, beyond surgical removal of the tumour, there is currently no curative therapy available, especially for its advanced stages. This may, in part, be owing to incomplete understanding of the molecular mechanisms that regulate the initiation and/or progression of melanoma to metastasis. The molecular mechanisms leading to the development and progression of melanoma are the focus of intense investigation, and many genetic/epigenetic alterations affecting melanoma progression and development have been identified. microRNAs (miRNAs) are emerging as important causal modulators in the development and progression of melanoma. The understanding of miRNA-mediated regulation of tumours has grown immensely over the last few years, as it has been understood to regulate most biological processes. Here, we review the currently available data on miRNAs associated with melanoma, highlighting those deregulated miRNAs that target important genes and pathways involved in the progression of melanocytes to primary and metastatic melanoma. We also review their potential clinical utility as biomarkers and potential use in targeted therapy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Biomarkers, Tumor / metabolism
  • Cell Transformation, Neoplastic / pathology
  • Down-Regulation / physiology
  • Early Detection of Cancer
  • Epigenesis, Genetic / physiology
  • Genes, Tumor Suppressor / physiology
  • Humans
  • Melanoma / diagnosis
  • Melanoma / etiology*
  • MicroRNAs / physiology*
  • Microphthalmia-Associated Transcription Factor / physiology
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Prognosis
  • Skin Neoplasms / diagnosis
  • Skin Neoplasms / etiology*
  • Tumor Suppressor Protein p53 / metabolism
  • Up-Regulation / physiology

Substances

  • Biomarkers, Tumor
  • MITF protein, human
  • MicroRNAs
  • Microphthalmia-Associated Transcription Factor
  • Tumor Suppressor Protein p53