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G-quadruplex ligands as potent regulators of lysosomes.
Ferret, Lucille; Alvarez-Valadez, Karla; Rivière, Jennifer; Muller, Alexandra; Bohálová, Natalia; Yu, Luo; Guittat, Lionel; Brázda, Vaclav; Kroemer, Guido; Mergny, Jean-Louis; Djavaheri-Mergny, Mojgan.
Afiliação
  • Ferret L; Centre de Recherche des Cordeliers, INSERM UMRS 1138, Sorbonne Université, Université Paris Cité, Equipe labellisée par la Ligue contre le Cancer, Institut universitaire de France, Paris, France.
  • Alvarez-Valadez K; Metabolomics and Cell Biology Platforms, Institut Gustave Roussy, Villejuif, France.
  • Rivière J; Centre de Recherche des Cordeliers, INSERM UMRS 1138, Sorbonne Université, Université Paris Cité, Equipe labellisée par la Ligue contre le Cancer, Institut universitaire de France, Paris, France.
  • Muller A; Metabolomics and Cell Biology Platforms, Institut Gustave Roussy, Villejuif, France.
  • Bohálová N; Department of Medicine III, Klinikum Rechts der Isar, Technical University of Munich, Munich, Germany.
  • Yu L; Centre de Recherche des Cordeliers, INSERM UMRS 1138, Sorbonne Université, Université Paris Cité, Equipe labellisée par la Ligue contre le Cancer, Institut universitaire de France, Paris, France.
  • Guittat L; Metabolomics and Cell Biology Platforms, Institut Gustave Roussy, Villejuif, France.
  • Brázda V; Department of Biophysical Chemistry and Molecular Oncology, Institute of Biophysics, The Czech Academy of Sciences, Brno, Czech Republic.
  • Kroemer G; Laboratoire d'Optique et Biosciences, Ecole Polytechnique, CNRS, INSERM, Institut Polytechnique de Paris, 91128 Palaiseau, France.
  • Mergny JL; CNRS UMR9187, INSERM U1196, Université Paris-Saclay, Orsay, France.
  • Djavaheri-Mergny M; Laboratoire d'Optique et Biosciences, Ecole Polytechnique, CNRS, INSERM, Institut Polytechnique de Paris, 91128 Palaiseau, France.
Autophagy ; 19(7): 1901-1915, 2023 07.
Article em En | MEDLINE | ID: mdl-36740766
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Autofagia / Quadruplex G Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Autofagia / Quadruplex G Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article