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Coming of age: could obesity-related metabolic complications be treated by targeting senescent cells?

作者信息

Kasperova Barbora Judita, Cinkajzlova Anna, Horvath Ludek, Svoboda Petr, Haluzik Martin, Stemberkova Hubackova Sona

机构信息

Diabetes Centre, Institute for Clinical and Experimental Medicine, Prague, Czechia.

First Faculty of Medicine, Charles University in Prague, Prague, Czechia.

出版信息

Front Cell Dev Biol. 2025 Jun 4;13:1622107. doi: 10.3389/fcell.2025.1622107. eCollection 2025.

DOI:10.3389/fcell.2025.1622107
PMID:40535573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12174156/
Abstract

Aging is characterized by gradual deterioration of organ or tissue function and its ability to maintain homeostasis of the different physiological processes. This leads to the development of structural and functional alterations accompanied by an increased risk for diverse pathologies. Cellular senescence is a controlled biological process that could contribute to the development of many age-related diseases and related metabolic dysfunctions. Two major chronic diseases associated with premature accumulation of senescent cells that impose an enormous burden on global health systems are obesity and type 2 diabetes mellitus with its related complications. The purpose of this review is to highlight the links between aging, obesity, and type 2 diabetes mellitus, focusing on the role of cellular senescence in disease development and progression. Additionally, this review will discuss the potential of targeting cellular senescence as a promising therapeutic strategy for managing these interrelated diseases, therefore offering a novel approach to prevention and treatment.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/12174156/a0f4d089346a/fcell-13-1622107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/12174156/36150272bb4c/fcell-13-1622107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/12174156/a26616db9212/fcell-13-1622107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/12174156/a0f4d089346a/fcell-13-1622107-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/12174156/36150272bb4c/fcell-13-1622107-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/12174156/a26616db9212/fcell-13-1622107-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/12174156/a0f4d089346a/fcell-13-1622107-g003.jpg

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本文引用的文献

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Nat Commun. 2025 Mar 28;16(1):3038. doi: 10.1038/s41467-025-57616-w.
2
Targeting Mitochondrial Integrity as a New Senolytic Strategy.以线粒体完整性为靶点的新型衰老细胞清除策略
Aging Dis. 2025 Feb 8. doi: 10.14336/AD.2024.1100.
3
Estimated Burden of Metabolic Dysfunction-Associated Steatotic Liver Disease in US Adults, 2020 to 2050.2020年至2050年美国成年人中代谢功能障碍相关脂肪性肝病的估计负担
JAMA Netw Open. 2025 Jan 2;8(1):e2454707. doi: 10.1001/jamanetworkopen.2024.54707.
4
Senescent cell depletion alleviates obesity-related metabolic and cardiac disorders.衰老细胞耗竭可缓解肥胖相关的代谢和心脏疾病。
Mol Metab. 2025 Jan;91:102065. doi: 10.1016/j.molmet.2024.102065. Epub 2024 Nov 16.
5
Pharmacological Treatment of Obesity in Older Adults.老年人肥胖的药物治疗。
Drugs Aging. 2024 Nov;41(11):881-896. doi: 10.1007/s40266-024-01150-9. Epub 2024 Nov 8.
6
Tirzepatide's role in targeting adipose tissue macrophages to reduce obesity-related inflammation and improve insulin resistance.替尔泊肽通过靶向脂肪组织巨噬细胞减少肥胖相关炎症和改善胰岛素抵抗的作用。
Int Immunopharmacol. 2024 Dec 25;143(Pt 2):113499. doi: 10.1016/j.intimp.2024.113499. Epub 2024 Oct 29.
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