Oligonucleotides Targeting Telomeres and Telomerase in Cancer

Molecules. 2018 Sep 5;23(9):2267. doi: 10.3390/molecules23092267.

Abstract

Telomeres and telomerase have become attractive targets for the development of anticancer therapeutics due to their involvement in cancer cell immortality. Currently, several therapeutics have been developed that directly target telomerase and telomeres, such as telomerase inhibitors and G-quadruplex stabilizing ligands. Telomere-specific oligonucleotides that reduce telomerase activity and disrupt telomere architecture are also in development as novel anticancer therapeutics. Specifically, GRN163L and T-oligos have demonstrated promising anticancer activity in multiple cancers types via induction of potent DNA damage responses. Currently, several miRNAs have been implicated in the regulation of telomerase activity and may prove to be valuable targets in the development of novel therapies by reducing expression of telomerase subunits. Targeting miRNAs that are known to increase expression of telomerase subunits may be another strategy to reduce carcinogenesis. This review aims to provide a comprehensive understanding of current oligonucleotide-based anticancer therapies that target telomeres and telomerase. These studies may help design novel therapeutic approaches to overcome the challenges of oligonucleotide therapy in a clinical setting.

Keywords: GRN163L; T-oligo; imetelstat; miRNA; telomerase; telomere.

Publication types

  • Review

MeSH terms

  • Animals
  • Gene Expression Regulation, Neoplastic
  • Gene Silencing
  • Gene Targeting*
  • Genetic Therapy
  • Humans
  • MicroRNAs / genetics
  • Molecular Targeted Therapy
  • Neoplasms / genetics*
  • Neoplasms / metabolism
  • Neoplasms / therapy
  • Oligonucleotides / chemistry
  • Oligonucleotides / genetics*
  • Oligonucleotides / therapeutic use
  • RNA Interference
  • Telomerase / antagonists & inhibitors
  • Telomerase / genetics*
  • Telomerase / metabolism
  • Telomere / genetics*
  • Telomere / metabolism

Substances

  • MicroRNAs
  • Oligonucleotides
  • Telomerase