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Molecular inhibition of RAS signalling to target ageing and age-related health.
Laskovs, Mihails; Partridge, Linda; Slack, Cathy.
Afiliación
  • Laskovs M; School of Biosciences, College of Health and Life Sciences, Aston University, Birmingham B4 7ET, UK.
  • Partridge L; Institute of Healthy Ageing, Department of Genetics, Evolution and Environment, University College London, Darwin Building, Gower Street, London WC1E 6BT, UK.
  • Slack C; Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Strasse 9b, 50931 Cologne, Germany.
Dis Model Mech ; 15(10)2022 10 01.
Article en En | MEDLINE | ID: mdl-36111627
The RAS/MAPK pathway is a highly conserved signalling pathway with a well-established role in cancer. Mutations that hyperactivate this pathway are associated with unregulated cell proliferation. Evidence from a range of model organisms also links RAS/MAPK signalling to ageing. Genetic approaches that reduce RAS/MAPK signalling activity extend lifespan and also improve healthspan, delaying the onset and/or progression of age-related functional decline. Given its role in cancer, therapeutic interventions that target and inhibit this pathway's key components are under intense investigation. The consequent availability of small molecule inhibitors raises the possibility of repurposing these compounds to ameliorate the deleterious effects of ageing. Here, we review evidence that RAS/MAPK signalling inhibitors already in clinical use, such as trametinib, acarbose, statins, metformin and dihydromyricetin, lead to lifespan extension and to improved healthspan in a range of model systems. These findings suggest that the repurposing of small molecule inhibitors of RAS/MAPK signalling might offer opportunities to improve health during ageing, and to delay or prevent the development of age-related disease. However, challenges to this approach, including poor tolerance to treatment in older adults or development of drug resistance, first need to be resolved before successful clinical implementation.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Inhibidores de Hidroximetilglutaril-CoA Reductasas / Metformina / Neoplasias / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Aged / Humans Idioma: En Revista: Dis Model Mech Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Inhibidores de Hidroximetilglutaril-CoA Reductasas / Metformina / Neoplasias / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Aged / Humans Idioma: En Revista: Dis Model Mech Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article