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Procyanidin C1 is a natural agent with senolytic activity against aging and age-related diseases
Open accessPreprint — published as 10.1038/s42255-021-00491-8 · Paper page
Abstract
Aging causes functional decline of multiple organs and increases the risk of age-related pathologies. In advanced lives, accumulation of senescent cells, which develop the senescence-associated secretory phenotype (SASP), promotes chronic inflammation and causes diverse conditions. Here we report the frontline outcome of screening a natural product library with human primary stromal cells as an experimental model. Multiple candidate compounds were assayed, and grape seed extract (GSE) was selected for further investigation due to its leading capacity in targeting senescent cells. We found procyanidin C1 (PCC1), a polyphenolic component, plays a critical role in mediating the antiaging effects of GSE. PCC1 blocks the SASP expression when used at low concentrations. Importantly, it selectively kills senescent cells upon application at higher concentrations, mainly by enhancing production of reactive oxygen species (ROS) and disturbing mitochondrial membrane potential, processes accompanied by upregulation of Bcl-2 family pro-apoptotic factors Puma and Noxa in senescent cells. PCC1 depletes senescent cells in treatment-damaged tumor microenvironment (TME) and enhances therapeutic efficacy when combined with chemotherapy in preclinical assays. Intermittent administration of PCC1 to both senescent cell-implanted mice and naturally aged animals alleviated physical dysfunction and prolonged post-treatment survival, thus providing substantial benefits in late life stage. Together, our study identifies PCC1 as a distinct natural senolytic agent, which may be exploited to delay aging and control age-related pathologies in future medicine.
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References 77 · Cited by 341
Metadata
- Authors
- Xu, Q., Fu, Q., Li, Z., Liu, H., Wang, Y., Lin, X., He, R., Zhang, X., Campisi, J., Kirkland, J., & Sun, Y.
- Affiliations
- Shanghai Jiao Tong University (CN)
- Binzhou Medical University (CN)
- Chinese Academy of Sciences (CN)
- Shanghai Institute of Nutrition and Health (CN)
- Science & Technology Centre, By-Health Co., Ltd
- Buck Institute for Research on Aging (US)
- Mayo Clinic (US)
- Corresponding author
- Sun, Yu
- ORCID
- Venue
- Nature Metabolism
- Published
- 2021-04-20
- Volume
- 3
- Issue
- 12
- Pages
- 1706-1726
- ISSN
- 2522-5812 (ISSN-L)
- PMC
- PMC8688144
- OpenAlex
- W4200000184
- Cited by
- 341
- References
- 77
- Citations by year
- 2026: 66 · 2025: 103 · 2024: 73 · 2023: 54 · 2022: 43 · 2021: 2
- FWCI
- 26.98
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Nature Metabolism (publishedVersion, cc-by)
- Research Square (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion, cc-by)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- Funders
- Noaber Foundation
- National Natural Science Foundation of China (31671425, 31871380, 201706, XDB39010500, 81472709, 31671425, 31871380, 82130045, #2017YFA0103302, 2020-08, 82130045, 91749203, 81571512, 81472709, 31671425, 31871380, 2016YFC1302400, 81370730, 81472709, 92049304, 82030039)
- Chinese Academy of Sciences (202008, XDB39010500)
- National Institutes of Health (AG013925, AG062413)
- National Key Research and Development Program of China (2017YFA0103302, 202008, 2020YFC2002800, 2016YFA0100602, 2016YFC1302400)
- National Institute on Aging (R01AG013925, R37AG013925, P01AG062413)
- DOD Prostate Cancer Research Program (PC111703)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › 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
- procyanidin C1, grape seed extract, senolytics, senescence-associated secretory phenotype, senescent cells, lifespan extension, healthspan, aging, reactive oxygen species, mitochondrial dysfunction, tumor microenvironment, combination chemotherapy, flavonoids, natural products
- MeSH terms
- Drug Development, Senescence-Associated Secretory Phenotype, Senotherapeutics, Animals, Cell Line, Energy Metabolism, Flavonoids, Gene Expression Regulation, Humans, Longevity, Mitochondria, Cellular Senescence, Apoptosis, Oxidative Stress, Computational Biology, Gene Expression Profiling, Mice
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