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  Molecular inhibition of RAS signalling to target ageing and age-related health

Laskovs, M., Partridge, L., & Slack, C. (2022). Molecular inhibition of RAS signalling to target ageing and age-related health. Dis Model Mech, 15(10). doi:10.1242/dmm.049627.

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Laskovs, M., Author
Partridge, L.1, Author           
Slack, C., Author
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1Department Partridge - Biological Mechanisms of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_1942287              

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Free keywords: Acarbose/therapeutic use Aged *Antineoplastic Agents/pharmacology Humans *Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use *Metformin *Neoplasms/drug therapy/metabolism ras Proteins/genetics Ageing MEK inhibitor RAS pathway
 Abstract: 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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 Dates: 2022-10-012022-09-16
 Publication Status: Issued
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 Identifiers: Other: 36111627
DOI: 10.1242/dmm.049627
ISSN: 1754-8411 (Electronic)1754-8403 (Linking)
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Title: Dis Model Mech
Source Genre: Journal
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Pages: - Volume / Issue: 15 (10) Sequence Number: - Start / End Page: - Identifier: -