Cited by 237Telomeres, Telomerase, and SenescenceGenetics, Aging, and Longevity in Model OrganismsSirtuins and Resveratrol in Medicine

Senolytic therapies for healthy longevity.

Open access
van Deursen, Jan M.·2019·Science

Abstract

Clearing senescent cells with targeted drugs could combat age-associated disease

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Crossref · 10.1126/science.aaw1299

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  • D + Q and the BCL-2 inhibitors ABT-263 and ABT-737 are the most frequently used senolytics in vivo, showing promise in improving a wide range of pathologies.

    “D + Q and the BCL-2 inhibitors, ABT-263 (Navitoclax) and ABT-737, are the most frequently used senolytics in vivo, showing promise in improving a wide range of pathologies (van Deursen 2019).”

    From Senescence and the SASP: many therapeutic avenues (2020) · cites this paper as van Deursen 2019

    In “Clearing senescent cells with targeted drugs to combat age-related disease” (page unavailable), the paper identifies ABT-263 and ABT-737 as senolytics, mentions dasatinib with quercetin, and reports that ABT-263 attenuated disease phenotypes in mouse models of atherosclerosis and neurodegeneration. It does not say these are the most frequently used senolytics in vivo or establish improvements across a wide range of pathologies for all three treatments. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • ABT-263 and ABT-737 are the most frequently used senolytics in vivo and show promise in improving a wide range of pathologies.

    “ABT-737, are the most frequently used senolytics in vivo, showing promise in improving a wide range of pathologies (van Deursen 2019).”

    From Senescence and the SASP: many therapeutic avenues (2020) · cites this paper as van Deursen 2019

    In “Clearing senescent cells with targeted drugs to combat age-related disease” (page not available), the paper identifies ABT-263 and ABT-737 as senolytics and reports that ABT-263 attenuated disease phenotypes in mouse models of atherosclerosis and neurodegeneration. It does not say these are the most frequently used senolytics in vivo or establish improvements across a wide range of pathologies for both drugs. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • Accumulating evidence has demonstrated that both anti-senescence and pro-senescence therapies could be beneficial depending on the context.

    “Accumulating evidence has demonstrated that both anti-senescence and pro-senescence therapies could be beneficial depending on the context (Myrianthopoulos et al., 2019; van Deursen, 2019).”

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References 16 · Cited by 237

Research works printed but not linked: 2

  1. [11]Munoz-Espin D, EMBO Mol Med 10, (2018). PMC6127887 30012580
  2. [14]Munoz-Espin D, Cell 155, 1104– 1118 (2013). 24238962

Authors
van Deursen, J. M.
Affiliations
Departments of Biochemistry and Molecular Biology, and Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Venue
Science
Published
2019-05-17
Volume
364
Issue
6441
Pages
636-637
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2946521685
Cited by
237
References
16
Citations by year
2026: 16 · 2025: 19 · 2024: 42 · 2023: 37 · 2022: 42 · 2021: 36 · 2020: 36 · 2019: 9
FWCI
21.09
Type
journal article
Language
en
Open access
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institute on Aging (R01AG057493)
  • National Cancer Institute (R01CA096985)
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, senescent cells, cellular senescence, healthy aging, age-related diseases
MeSH terms
Healthy Aging, Animals, Humans, Longevity, Neoplasms, Rejuvenation, Cellular Senescence, Apoptosis, Neurodegenerative Diseases, Models, Animal, Atherosclerosis, Mice

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