DNA methylation and chromatin modifiers in colorectal cancer

Mol Aspects Med. 2019 Oct:69:73-92. doi: 10.1016/j.mam.2019.04.002. Epub 2019 Apr 30.

Abstract

Colorectal carcinogenesis is a multistep process involving the accumulation of genetic alterations over time that ultimately leads to disease progression and metastasis. Binding of transcription factors to gene promoter regions alone cannot explain the complex regulation pattern of gene expression during this process. It is the chromatin structure that allows for a high grade of regulatory flexibility for gene expression. Posttranslational modifications on histone proteins such as acetylation, methylation, or phosphorylation determine the accessibility of transcription factors to DNA. DNA methylation, a chemical modification of DNA that modulates chromatin structure and gene transcription acts in concert with these chromatin conformation alterations. Another epigenetic mechanism regulating gene expression is represented by small non-coding RNAs. Only very recently epigenetic alterations have been included in molecular subtype classification of colorectal cancer (CRC). In this chapter, we will provide examples of the different epigenetic players, focus on their role for epithelial-mesenchymal transition and metastatic processes and discuss their prognostic value in CRC.

Keywords: Chromatin remodeling; Colorectal cancer; DNA methylation; Epigenetics; Epithelial-to-mesenchymal transition; Histone modifications; Prognosis; Stemness; miRNA.

Publication types

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

MeSH terms

  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / metabolism
  • Chromatin / genetics*
  • Chromatin / metabolism
  • Chromatin Assembly and Disassembly / genetics
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology
  • DNA Methylation*
  • Disease Progression
  • Epigenesis, Genetic*
  • Epistasis, Genetic
  • Epithelial-Mesenchymal Transition
  • Gene Expression Regulation, Neoplastic
  • Histones / metabolism
  • Humans
  • Protein Processing, Post-Translational

Substances

  • Chromatin
  • Histones