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衰老相关分泌表型与骨质疏松症的最新进展

Recent advances in senescence-associated secretory phenotype and osteoporosis.

作者信息

Fan Haonan, Qiao Zhi, Li Jitian, Shang Guowei, Shang Chunfeng, Chen Songfeng, Leng Zikuan, Su Huifang, Kou Hongwei, Liu Hongjian

机构信息

Department of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.

Henan Luoyang Orthopedic Hospital (Henan Provincial Orthopedic Hospital)/Henan Institute of Orthopedic and Traumatology, Luoyang 471000, China.

出版信息

Heliyon. 2024 Feb 8;10(4):e25538. doi: 10.1016/j.heliyon.2024.e25538. eCollection 2024 Feb 29.

DOI:10.1016/j.heliyon.2024.e25538
PMID:38375248
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10875379/
Abstract

The worldwide elderly population is on the rise, and aging is a major osteoporosis risk factor. Senescent cells accumulation can have a detrimental effect the body as we age. The senescence-associated secretory phenotype (SASP), an essential cellular senescence hallmark, is an important mechanism connecting cellular senescence to osteoporosis. This review describes in detail the characteristics of SASPs and their regulatory agencies, and shed fresh light on how SASPs from different senescent cells contribute to osteoporosis development. Furthermore, we summarized various innovative therapy techniques that target SASPs to lower the burden of osteoporosis in the elderly and discussed the potential challenges of SASPs-based therapy for osteoporosis as a new clinical trial.

摘要

全球老年人口正在增加,而衰老 是骨质疏松症的一个主要风险因素。随着我们年龄的增长,衰老细胞的积累会对身体产生有害影响。衰老相关分泌表型(SASP)是细胞衰老的一个重要标志,是将细胞衰老与骨质疏松症联系起来的重要机制。本文详细描述了SASP的特征及其调控机制,并对来自不同衰老细胞的SASP如何促进骨质疏松症的发展有了新的认识。此外,我们总结了各种针对SASP的创新治疗技术,以减轻老年人骨质疏松症的负担,并讨论了作为一项新的临床试验,基于SASP的骨质疏松症治疗的潜在挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815d/10875379/c95aa061e7cd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815d/10875379/b1938177a8b9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815d/10875379/c3c1b73d67cc/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815d/10875379/c95aa061e7cd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815d/10875379/b1938177a8b9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815d/10875379/c3c1b73d67cc/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/815d/10875379/c95aa061e7cd/gr3.jpg

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Bioact Mater. 2023 Jan 20;25:13-28. doi: 10.1016/j.bioactmat.2023.01.009. eCollection 2023 Jul.
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Astaxanthin attenuates irradiation-induced osteoporosis in mice by inhibiting oxidative stress, osteocyte senescence, and SASP.虾青素通过抑制氧化应激、骨细胞衰老和 SASP 来减轻小鼠辐射诱导的骨质疏松症。
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The effects of fisetin on bone and cartilage: A systematic review.
细胞衰老:从稳态到病理影响及治疗策略
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Cellular senescence in the tumor with a bone niche microenvironment: friend or foe?具有骨龛微环境的肿瘤中的细胞衰老:朋友还是敌人?
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Nonlinear relationship between cardiometabolic index and bone mineral density in U.S. adults: the mediating role of percent body fat.美国成年人中心血管代谢指数与骨密度的非线性关系:体脂百分比的中介作用。
Sci Rep. 2024 Sep 28;14(1):22449. doi: 10.1038/s41598-024-73427-3.
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BMC Med Genomics. 2024 Mar 5;17(1):70. doi: 10.1186/s12920-024-01837-3.
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