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G-quadruplex ligands as potent regulators of lysosomes

  • Lucille Ferret
  • , Karla Alvarez-Valadez
  • , Jennifer Rivière
  • , Alexandra Muller
  • , Natalia Bohálová
  • , Luo Yu
  • , Lionel Guittat
  • , Vaclav Brázda
  • , Guido Kroemer
  • , Jean Louis Mergny
  • , Mojgan Djavaheri-Mergny
  • Sorbonne Université
  • Gustave Roussy Comprehensive Cancer Institute
  • Klinikum rechts der Isar der Technischen Universität München
  • V.v.i.
  • Institut Polytechnique de Paris
  • Université Paris-Saclay
  • University Paris 13
  • Pôle de Biologie

Résultats de recherche: Contribution à un journalArticle de révisionRevue par des pairs

Résumé

Guanine-quadruplex structures (G4) are unusual nucleic acid conformations formed by guanine-rich DNA and RNA sequences and known to control gene expression mechanisms, from transcription to protein synthesis. So far, a number of molecules that recognize G4 have been developed for potential therapeutic applications in human pathologies, including cancer and infectious diseases. These molecules are called G4 ligands. When the biological effects of G4 ligands are studied, the analysis is often limited to nucleic acid targets. However, recent evidence indicates that G4 ligands may target other cellular components and compartments such as lysosomes and mitochondria. Here, we summarize our current knowledge of the regulation of lysosome by G4 ligands, underlying their potential functional impact on lysosome biology and autophagic flux, as well as on the transcriptional regulation of lysosomal genes. We outline the consequences of these effects on cell fate decisions and we systematically analyzed G4-prone sequences within the promoter of 435 lysosome-related genes. Finally, we propose some hypotheses about the mechanisms involved in the regulation of lysosomes by G4 ligands.

langue originaleAnglais
Pages (de - à)1901-1915
Nombre de pages15
journalAutophagy
Volume19
Numéro de publication7
Les DOIs
étatPublié - 1 janv. 2023

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