Using Chemical Epigenetics to Target Cancer

Mol Cell. 2020 Jun 18;78(6):1086-1095. doi: 10.1016/j.molcel.2020.04.023. Epub 2020 May 13.

Abstract

Transcription is epigenetically regulated by the orchestrated function of chromatin-binding proteins that tightly control the expression of master transcription factors, effectors, and supportive housekeeping genes required for establishing and propagating the normal and malignant cell state. Rapid advances in chemical biology and functional genomics have facilitated exploration of targeting epigenetic proteins, yielding effective strategies to target transcription while reducing toxicities to untransformed cells. Here, we review recent developments in conventional active site and allosteric inhibitors, peptidomimetics, and novel proteolysis-targeted chimera (PROTAC) technology that have deepened our understanding of transcriptional processes and led to promising preclinical compounds for therapeutic translation, particularly in cancer.

Keywords: PROTAC; chromatin; degrader; epigenetics; inhibitor; peptidomimetic; transcription.

Publication types

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

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Chromatin / genetics
  • Chromatin / metabolism
  • Epigenesis, Genetic / drug effects*
  • Epigenesis, Genetic / genetics*
  • Epigenesis, Genetic / physiology
  • Epigenomics / methods
  • Humans
  • Neoplasms / genetics*
  • Neoplasms / therapy
  • Proteolysis / drug effects
  • Transcription Factors / metabolism

Substances

  • Antineoplastic Agents
  • Chromatin
  • Transcription Factors