The Clinical Potential of Senolytic Drugs
- PMID: 28869295
- PMCID: PMC5641223
- DOI: 10.1111/jgs.14969
The Clinical Potential of Senolytic Drugs
Abstract
Senolytic drugs are agents that selectively induce apoptosis of senescent cells. These cells accumulate in many tissues with aging and at sites of pathology in multiple chronic diseases. In studies in animals, targeting senescent cells using genetic or pharmacological approaches delays, prevents, or alleviates multiple age-related phenotypes, chronic diseases, geriatric syndromes, and loss of physiological resilience. Among the chronic conditions successfully treated by depleting senescent cells in preclinical studies are frailty, cardiac dysfunction, vascular hyporeactivity and calcification, diabetes mellitus, liver steatosis, osteoporosis, vertebral disk degeneration, pulmonary fibrosis, and radiation-induced damage. Senolytic agents are being tested in proof-of-concept clinical trials. To do so, new clinical trial paradigms for testing senolytics and other agents that target fundamental aging mechanisms are being developed, because use of long-term endpoints such as lifespan or healthspan is not feasible. These strategies include testing effects on multimorbidity, accelerated aging-like conditions, diseases with localized accumulation of senescent cells, potentially fatal diseases associated with senescent cell accumulation, age-related loss of physiological resilience, and frailty. If senolytics or other interventions that target fundamental aging processes prove to be effective and safe in clinical trials, they could transform geriatric medicine by enabling prevention or treatment of multiple diseases and functional deficits in parallel, instead of one at a time.
Keywords: SCAPs; cellular senescence; chronic diseases; geroscience hypothesis; senolytics.
© 2017, Copyright the Authors Journal compilation © 2017, The American Geriatrics Society.
Conflict of interest statement
Similar articles
-
Cellular Senescence: A Translational Perspective.EBioMedicine. 2017 Jul;21:21-28. doi: 10.1016/j.ebiom.2017.04.013. Epub 2017 Apr 12. EBioMedicine. 2017. PMID: 28416161 Free PMC article. Review.
-
The Achilles' heel of senescent cells: from transcriptome to senolytic drugs.Aging Cell. 2015 Aug;14(4):644-58. doi: 10.1111/acel.12344. Epub 2015 Apr 22. Aging Cell. 2015. PMID: 25754370 Free PMC article.
-
New agents that target senescent cells: the flavone, fisetin, and the BCL-XL inhibitors, A1331852 and A1155463.Aging (Albany NY). 2017 Mar 8;9(3):955-963. doi: 10.18632/aging.101202. Aging (Albany NY). 2017. PMID: 28273655 Free PMC article.
-
Senolytic drugs in respiratory medicine: is it an appropriate therapeutic approach?Expert Opin Investig Drugs. 2018 Jul;27(7):573-581. doi: 10.1080/13543784.2018.1492548. Epub 2018 Jul 4. Expert Opin Investig Drugs. 2018. PMID: 29972333 Review.
-
Chronic senolytic treatment alleviates established vasomotor dysfunction in aged or atherosclerotic mice.Aging Cell. 2016 Oct;15(5):973-7. doi: 10.1111/acel.12458. Epub 2016 Aug 5. Aging Cell. 2016. PMID: 26864908 Free PMC article.
Cited by
-
Periodontal Disease and Senescent Cells: New Players for an Old Oral Health Problem?Int J Mol Sci. 2020 Oct 9;21(20):7441. doi: 10.3390/ijms21207441. Int J Mol Sci. 2020. PMID: 33050175 Free PMC article. Review.
-
Effect of Selected Antioxidants on the In Vitro Aging of Human Fibroblasts.Int J Mol Sci. 2024 Jan 26;25(3):1529. doi: 10.3390/ijms25031529. Int J Mol Sci. 2024. PMID: 38338809 Free PMC article.
-
Cobalamin Deficiency May Induce Astrosenescence-An In Vitro Study.Cells. 2022 Oct 28;11(21):3408. doi: 10.3390/cells11213408. Cells. 2022. PMID: 36359805 Free PMC article.
-
Selective Vulnerability of Senescent Glioblastoma Cells to BCL-XL Inhibition.Mol Cancer Res. 2022 Jun 3;20(6):938-948. doi: 10.1158/1541-7786.MCR-21-0029. Mol Cancer Res. 2022. PMID: 35191501 Free PMC article.
-
Antiaging agents: safe interventions to slow aging and healthy life span extension.Nat Prod Bioprospect. 2022 May 9;12(1):18. doi: 10.1007/s13659-022-00339-y. Nat Prod Bioprospect. 2022. PMID: 35534591 Free PMC article. Review.
References
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
