microRNA expression and biogenesis in cellular response to ionizing radiation

DNA Cell Biol. 2014 Oct;33(10):667-79. doi: 10.1089/dna.2014.2401. Epub 2014 Jun 6.

Abstract

Increasing evidence demonstrates that the expression levels of microRNAs (miRNAs) significantly change upon ionizing radiation (IR) and play a critical role in cellular response to IR. Although several radiation responsive miRNAs and their targets have been identified, little is known about how miRNAs expression and biogenesis is regulated by IR-caused DNA damage response (DDR). Hence, in this review, we summarize miRNA expression and biogenesis in cellular response to IR and mainly elucidate the regulatory mechanisms of miRNA expression and biogenesis from different aspects including ataxia-telangiectasia mutated (ATM) kinase, p53/p63/p73 family and other potential factors. Furthermore, we focus on ΔNp73, which might be a potential regulator of miRNA expression and biogenesis in cellular response to IR. miRNAs could effectively activate the IR-induced DDR and modulate the radiation response and cellular radiosensitivity, which have an important potential clinical application. Therefore, thoroughly understanding the regulatory mechanisms of miRNAs expression and biogenesis in radiation response will provide new insights for clinical cancer radiotherapy.

Publication types

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

MeSH terms

  • Ataxia Telangiectasia Mutated Proteins / metabolism
  • DNA Damage*
  • DNA Repair / radiation effects*
  • DNA-Binding Proteins / metabolism
  • Humans
  • MicroRNAs / biosynthesis*
  • MicroRNAs / radiation effects
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Neoplasms / radiotherapy*
  • Nuclear Proteins / metabolism
  • Transcription Factors / metabolism
  • Tumor Protein p73
  • Tumor Suppressor Protein p53 / metabolism
  • Tumor Suppressor Proteins / metabolism

Substances

  • DNA-Binding Proteins
  • MicroRNAs
  • Nuclear Proteins
  • TP63 protein, human
  • TP73 protein, human
  • Transcription Factors
  • Tumor Protein p73
  • Tumor Suppressor Protein p53
  • Tumor Suppressor Proteins
  • delta Np73 protein, human
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins