DNA Methylation Profiling of hTERT Gene Alongside with the Telomere Performance in Gastric Adenocarcinoma

J Gastrointest Cancer. 2020 Sep;51(3):788-799. doi: 10.1007/s12029-020-00427-7.

Abstract

Purpose: Epigenetic modification including of DNA methylation, histone acetylation, histone methylation, histon phosphorylation and non-coding RNA can impress the gene expression and genomic stability and cause different types of malignancies and also main human disorder. Conspicuously, the epigenetic alteration special DNA methylation controls telomere length, telomerase activity and also function of different genes particularly hTERT expression. Telomeres are important in increasing the lifespan, health, aging, and the development and progression of some diseases like cancer.

Methods: This review provides an assessment of the epigenetic alterations of telomeres, telomerase and repression of its catalytic subunit, hTERT and function of long non-coding RNAs such as telomeric-repeat containing RNA (TERRA) in carcinogenesis and tumorgenesis of gastric cancer.

Results: hTERT expression is essential and indispensable in telomerase activation through immortality and malignancies and also plays an important role in maintaining telomere length. Telomeres and telomerase have been implicated in regulating epigenetic factors influencing certain gene expression. Correspondingly, these changes in the sub telomere and telomere regions are affected by the shortening of telomere length and increased telomerase activity and hTERT gene expression have been observed in many cancers, remarkably in gastric cancer.

Conclusion: Epigenetic alteration and regulation of hTERT gene expression are critical in controlling telomerase activity and its expression. Graphical Abstract.

Keywords: Epigenetic; Human telomerase reverse transcriptase (hTERT); Telomerase; Telomere; Telomeric repeat-containing RNA (TERRA).

Publication types

  • Review

MeSH terms

  • Adenocarcinoma / genetics*
  • Carcinogenesis / genetics
  • DNA Methylation
  • Epigenesis, Genetic
  • Epigenomics
  • Gene Expression Regulation, Neoplastic*
  • Histone Code / genetics
  • Histones / metabolism
  • Humans
  • Promoter Regions, Genetic / genetics
  • RNA, Long Noncoding / metabolism
  • Stomach Neoplasms / genetics*
  • Telomerase / genetics*
  • Telomerase / metabolism
  • Telomere / metabolism*
  • Telomere Homeostasis / genetics

Substances

  • Histones
  • RNA, Long Noncoding
  • TERT protein, human
  • Telomerase