Cancerous miRNAs and their regulation

Cell Cycle. 2008 Jun 1;7(11):1529-38. doi: 10.4161/cc.7.11.5977. Epub 2008 Mar 20.

Abstract

Although they account for only a very minor fraction of the expressed genome, microRNAs (miRNAs) are pivotal regulators of development and cellular homeostasis through their control of diverse cellular processes including proliferation, differentiation, apoptosis, survival, motility and morphogenesis. Accordingly, several miRNAs have been functionally classified as proto-oncogenes or tumor suppressors and are aberrantly expressed in different cancer types. Deregulation (e.g., overexpression or loss of expression) of these so-called "cancerous" miRNAs can figure prominently in tumor initiation and progression by elaborating an inappropriate cellular program promoting uncontrolled proliferation, favoring survival, inhibiting differentiation and/or promoting invasive behavior. These features would certainly promote tumor dissemination and persistence by favoring metastasis and therapy resistance. Cancerous miRNAs therefore represent attractive molecules for exploitation as biomarkers and therapeutic targets. In this review, we highlight recently characterized cancerous miRNAs and the mechanisms through which they contribute to the pathogenesis of human cancers. We also discuss the signal transduction pathways that regulate the expression of these miRNAs with particular attention to several essential transcription factors such as Myc, p53 and the androgen receptor.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Biomarkers
  • Gene Expression Regulation, Neoplastic / genetics*
  • Humans
  • Interleukin-6 / metabolism
  • MicroRNAs / genetics
  • MicroRNAs / physiology*
  • NF-kappa B / metabolism
  • Neoplasms / genetics*
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction / physiology*
  • Transcription Factors / metabolism*

Substances

  • Biomarkers
  • Interleukin-6
  • MicroRNAs
  • NF-kappa B
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Transcription Factors