The DNA damage response and immune signaling alliance: Is it good or bad? Nature decides when and where

Pharmacol Ther. 2015 Oct:154:36-56. doi: 10.1016/j.pharmthera.2015.06.011. Epub 2015 Jul 3.

Abstract

The characteristic feature of healthy living organisms is the preservation of homeostasis. Compelling evidence highlight that the DNA damage response and repair (DDR/R) and immune response (ImmR) signaling networks work together favoring the harmonized function of (multi)cellular organisms. DNA and RNA viruses activate the DDR/R machinery in the host cells both directly and indirectly. Activation of DDR/R in turn favors the immunogenicity of the incipient cell. Hence, stimulation of DDR/R by exogenous or endogenous insults triggers innate and adaptive ImmR. The immunogenic properties of ionizing radiation, a prototypic DDR/R inducer, serve as suitable examples of how DDR/R stimulation alerts host immunity. Thus, critical cellular danger signals stimulate defense at the systemic level and vice versa. Disruption of DDR/R-ImmR cross talk compromises (multi)cellular integrity, leading to cell-cycle-related and immune defects. The emerging DDR/R-ImmR concept opens up a new avenue of therapeutic options, recalling the Hippocrates quote "everything in excess is opposed by nature."

Keywords: Autoimmunity; Cancer; DNA damage response and repair machinery; Immune response; Inflammation; Pattern recognition receptors.

Publication types

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

MeSH terms

  • DNA Damage / immunology*
  • DNA Repair / immunology*
  • DNA Virus Infections / immunology
  • Humans
  • Immunity, Cellular / immunology
  • Inflammation Mediators / immunology
  • NF-kappa B / immunology
  • RNA Virus Infections / immunology
  • Radiation, Ionizing
  • Signal Transduction / physiology*
  • Tumor Suppressor Protein p53 / immunology

Substances

  • Inflammation Mediators
  • NF-kappa B
  • Tumor Suppressor Protein p53