LncRNAs in DNA damage response and repair in cancer cells

Acta Biochim Biophys Sin (Shanghai). 2018 May 1;50(5):433-439. doi: 10.1093/abbs/gmy022.

Abstract

In order to maintain integrity of the genome, eukaryotic cells develop a complex DNA damage/repair response network, which can induce cell cycle arrest, apoptosis, or DNA repair. Chemo- and radiation therapies, which act primarily through the induction of DNA damage, are the most commonly used therapies for cancer. Impairment in the DNA damage response and repair system that protect cells from persistent DNA damage can affect the therapeutic efficacy of cancer. To date, accumulating evidence has suggested that long non-coding RNAs (lncRNAs) are involved in the regulation of the DNA damage/repair network. LncRNAs have been demonstrated to be master regulators of the genome at the transcriptional and post-transcriptional levels and play a key role in many physiological and pathological processes of cells. In this review, we will discuss the function of lncRNAs in regulating the cellular response to DNA damage.

Publication types

  • Review

MeSH terms

  • Apoptosis / genetics
  • Cell Cycle Checkpoints / genetics
  • DNA Damage*
  • DNA Repair*
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Models, Genetic
  • Neoplasms / genetics*
  • RNA, Long Noncoding / genetics*
  • Signal Transduction / genetics

Substances

  • RNA, Long Noncoding