Error-prone DNA repair pathways as determinants of immunotherapy activity: an emerging scenario for cancer treatment

Int J Cancer. 2020 Nov 15;147(10):2658-2668. doi: 10.1002/ijc.33038. Epub 2020 Jun 1.

Abstract

Defects in DNA repair machinery play a critical role in the pathogenesis and progression of human cancer. When they occur, the tumor cells activate error-prone mechanisms which lead to genomic instability and high mutation rate. These defects represent, therefore, a cancer Achilles'heel which could be therapeutically exploited by the use of DNA damage response inhibitors. Moreover, experimental and clinical evidence indicates that DNA repair deregulation has a pivotal role also in promoting immune recognition and immune destruction of cancer cells. Indeed, immune checkpoint inhibitors have received regulatory approval in tumors characterized by high genomic instability, such as melanomas and lung cancer. Here, we discuss how deregulation of DNA repair, through activation of error-prone mechanisms, increases immune activation against cancer. Finally, we address the potential strategies to use DNA repair components as biomarkers and/or therapeutic targets to empower immune-oncology treatment of human cancer.

Keywords: error-prone DNA repair; genomic instability; immune checkpoint inhibitors; precision oncology; predictive biomarkers.

Publication types

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

MeSH terms

  • Biomarkers, Tumor / genetics*
  • DNA Repair
  • DNA Repair Enzymes
  • Genomic Instability
  • Humans
  • Immune Checkpoint Inhibitors / pharmacology*
  • Immune Checkpoint Inhibitors / therapeutic use
  • Neoplasms / drug therapy*
  • Neoplasms / genetics

Substances

  • Biomarkers, Tumor
  • Immune Checkpoint Inhibitors
  • DNA Repair Enzymes