Ageing - Oxidative stress, PTMs and disease

T. Ebert*, N. Tran, L. Schurgers, P. Stenvinkel, P.G. Shiels

*Corresponding author for this work

Research output: Contribution to journal(Systematic) Review article peer-review

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Abstract

Post-translational modifications (PTMs) have been proposed as a link between the oxidative stress-inflammation ageing trinity, thereby affecting several hallmarks of ageing.Phosphorylation, acetylation, and ubiquitination cover >90% of all the reported PTMs. Several of the main PTMs are involved in normal "healthy" ageing and in different age-related diseases, for instance neurodegenerative, metabolic, cardiovascular, and bone diseases, as well as cancer and chronic kidney disease. Ultimately, data from human rare progeroid syndromes, but also from long-living animal species, imply that PTMs are critical regulators of the ageing process. Mechanistically, PTMs target epigenetic and non-epigenetic pathways during ageing. In particular, epigenetic histone modification has critical implications for the ageing process and can modulate lifespan. Therefore, PTM-based therapeutics appear to be attractive pharmaceutical candidates to reduce the burden of ageing-related diseases. Several phosphorylation and acetylation inhibitors have already been FDA-approved for the treatment of other diseases and offer a unique potential to investigate both beneficial effects and possible side-effects. As an example, the most well-studied senolytic compounds dasatinib and quercetin, which have already been tested in Phase 1 pilot studies, also act as kinase inhibitors, targeting cellular senescence and increasing lifespan. Future studies need to carefully determine the best PTM-based candidates for the treatment of the "diseasome of ageing".
Original languageEnglish
Article number101099
Number of pages9
JournalMolecular Aspects of Medicine
Volume86
DOIs
Publication statusPublished - 1 Aug 2022

Keywords

  • Healthy ageing
  • Inflammation
  • Nuclear factor erythroid 2-related factor 2
  • Oxidative stress
  • Post-translational modifications
  • Premature ageing
  • Senescence
  • GILFORD PROGERIA SYNDROME
  • CHRONIC KIDNEY-DISEASE
  • LONGEST-LIVING RODENT
  • POSTTRANSLATIONAL MODIFICATION
  • HISTONE ACETYLATION
  • COGNITIVE FUNCTIONS
  • LAMIN
  • LONGEVITY
  • CANCER
  • TRANSCRIPTION

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