A novel role of long non-coding RNAs in response to X-ray irradiation

Toxicol In Vitro. 2015 Dec 25;30(1 Pt B):536-44. doi: 10.1016/j.tiv.2015.09.007. Epub 2015 Sep 9.

Abstract

In the present study, the role of lncRNAs in response to radiation-induced DNA damage and oxidative stress were explored to improve our understanding of the biological pathways activated upon radiation-induced toxicity. The toxicity of X-ray radiation on human bronchial epithelial cell lines (HBE) was determined through a dose-dependent increase in ROS production and γ-H2AX formation and changes to lncRNA expression was observed and quantified using lncRNA-specific microarrays. 115 lncRNAs expression was increased in a dose-dependent manner following X-ray irradiation. Bioinformatic prediction algorithms determined that these lncRNAs significantly affect the p53 signaling pathway, and, more specifically, the BRCA 1 transcription factor and coding genes adjacent to BRCA 1. Our results highlight a previously uncharacterized role for lncRNAs to act via the p53-pathway in response to X-ray-induced DNA damage, and suggest lncRNAs may serve as novel indicators for radiation toxicity.

Keywords: BRCA 1; DNA damage; Long non-coding RNA (lncRNA); X-ray; p53.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • DNA Damage
  • Histones / analysis
  • Humans
  • RNA, Long Noncoding / physiology*
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / radiation effects
  • Tumor Suppressor Protein p53 / physiology
  • X-Rays

Substances

  • H2AX protein, human
  • Histones
  • RNA, Long Noncoding
  • Reactive Oxygen Species
  • Tumor Suppressor Protein p53