Recent advances in the discovery of senolytics
Open accessAbstract
The demonstration in model organisms that cellular senescence drives aging and age-related diseases has led to widespread efforts to identify compounds able to selectively kill senescent cells, termed senolytics. Approaches used to identify senolytics include bioinformatic analysis of senescent cell anti-apoptotic pathways (SCAPs) for drug development and screening of drugs libraries on different senescent cell types in culture. Alternatively, cytotoxic compounds can be made specific to senescent cells through a prodrug strategy such as linking the compound to a galactose moiety where toxicity is activated by lysosomal β-galactosidase. Identified senolytics can then be optimized through medicinal chemistry or linking to E3 targeting moieties to facilitate proteolysis of their targets. This review will provide an overview of approaches to identify senolytics and an update of the classes of senolytics identified to date.
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Targeting the cGAS-STING axis with the small-molecule STING inhibitor H-151 had a SASP-suppressing, senomorphic effect and led to reduced lung pathology and prolonged survival in a human ACE2-transgenic mouse model of COVID-19.
“Targeting of the cGAS–STING axis, which induces type I interferons and other SASP factors, with the small-molecule STING inhibitor H-151 had a SASP-suppressing, senomorphic effect28,121,128,129 and led to reduced lung pathology and prolonged survival in a human ACE2-transgenic mouse model of COVID-19 (ref.59).”
From COVID-19 and cellular senescence (2023) · cites this paper as [121]
Each senescent cell type may have unique features that enable drug targeting.
“As detailed by Zhang et al. (Zhang et al., 2021) each senescent cell type may have unique features that enable drug targeting.”
From Skeletal muscle aging, cellular senescence, and senotherapeutics: current knowledge and future directions (2021) · cites this paper as Zhang et al., 2021
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References 88 · Cited by 115
- Authors
- Zhang, L., Pitcher, L. E., Prahalad, V., Niedernhofer, L. J., & Robbins, P. D.
- Affiliations
- University of Minnesota (US)
- Corresponding author
- Robbins, Paul D.
- Venue
- Mechanisms of Ageing and Development
- Publisher
- Elsevier BV
- Published
- 2021-12
- Volume
- 200
- Pages
- 111587
- ISSN
- 0047-6374 (ISSN-L)
- PMC
- PMC8687661
- OpenAlex
- W3205240380
- Cited by
- 115
- References
- 88
- Citations by year
- 2026: 18 · 2025: 20 · 2024: 42 · 2023: 19 · 2022: 14 · 2021: 2
- FWCI
- 2.77
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Mechanisms of Ageing and Development (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Aging (P01AG043376, U19AG056278, P01AG062413, R01AG063543)
- Topics
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Keywords
- senolytics, cellular senescence, aging, age-related diseases, drug screening, prodrug strategy, galactose, lysosomal beta-galactosidase
- MeSH terms
- Drug Development, Senotherapeutics, Humans, Longevity, Cellular Senescence, Drug Discovery
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