Cancer Epigenetics, Tumor Immunity, and Immunotherapy

Trends Cancer. 2020 Jul;6(7):580-592. doi: 10.1016/j.trecan.2020.02.003. Epub 2020 Mar 31.

Abstract

Epigenetic mechanisms, including DNA methylation, histone post-translational modifications, and chromatin structure regulation, are critical for the interactions between tumor and immune cells. Emerging evidence shows that tumors commonly hijack various epigenetic mechanisms to escape immune restriction. As a result, the pharmaceutical modulation of epigenetic regulators, including 'writers', 'readers', 'erasers', and 'remodelers', is able to normalize the impaired immunosurveillance and/or trigger antitumor immune responses. Thus, epigenetic targeting agents are attractive immunomodulatory drugs and will have major impacts on immuno-oncology. Here, we discuss epigenetic regulators of the cancer-immunity cycle and current advances in developing epigenetic therapies to boost anticancer immune responses, either alone or in combination with current immunotherapies.

Keywords: antitumor immune responses; cancer epigenetics; cancer–immunity cycle; epigenetic drugs; immuno-oncology; immunotherapy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cell Line, Tumor
  • DNA Methylation / drug effects
  • DNA Methylation / immunology
  • Disease Models, Animal
  • Drug Synergism
  • Epigenesis, Genetic / drug effects
  • Epigenesis, Genetic / immunology*
  • Histones / genetics
  • Histones / metabolism
  • Humans
  • Immunomodulation / drug effects
  • Immunomodulation / genetics
  • Immunotherapy / methods*
  • Mice
  • Neoplasms / drug therapy*
  • Neoplasms / genetics
  • Neoplasms / immunology
  • Protein Processing, Post-Translational / drug effects
  • Protein Processing, Post-Translational / immunology
  • Tumor Escape / drug effects
  • Tumor Escape / genetics
  • Tumor Microenvironment / drug effects
  • Tumor Microenvironment / genetics*
  • Tumor Microenvironment / immunology

Substances

  • Histones