• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

与年龄相关的骨质疏松症:靶向细胞衰老。

Age Related Osteoporosis: Targeting Cellular Senescence.

机构信息

Medical Science and Human Medicine Study Programme, Karl Landsteiner University of Health Sciences, 3500 Krems an der Donau, Austria.

Department of Physical Medicine and Rehabilitation, Medical University of Vienna, 1090 Vienna, Austria.

出版信息

Int J Mol Sci. 2022 Feb 28;23(5):2701. doi: 10.3390/ijms23052701.

DOI:10.3390/ijms23052701
PMID:35269841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8910503/
Abstract

Age-related chronic diseases are an enormous burden to modern societies worldwide. Among these, osteoporosis, a condition that predisposes individuals to an increased risk of fractures, substantially contributes to increased mortality and health-care costs in elderly. It is now well accepted that advanced chronical age is one of the main risk factors for chronical diseases. Hence, targeting fundamental aging mechanisms such as senescence has become a promising option in the treatment of these diseases. Moreover, for osteoporosis, the main pathophysiological concepts arise from menopause causing estrogen deficiency, and from aging. Here, we focus on recent advances in the understanding of senescence-related mechanisms contributing to age-related bone loss. Furthermore, treatment options for senile osteoporosis targeting senescent cells are reviewed.

摘要

与年龄相关的慢性疾病是全球现代社会的沉重负担。在这些疾病中,骨质疏松症使个体易骨折的风险增加,这大大增加了老年人的死亡率和医疗保健成本。现在人们普遍认为,高龄是慢性疾病的主要危险因素之一。因此,针对衰老等基本衰老机制已成为治疗这些疾病的一种有前途的选择。此外,对于骨质疏松症,主要的病理生理概念源于绝经引起的雌激素缺乏和衰老。在这里,我们专注于理解与年龄相关的骨丢失相关的衰老相关机制的最新进展。此外,还回顾了针对衰老细胞的治疗老年性骨质疏松症的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e88/8910503/56ebcb3ed25b/ijms-23-02701-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e88/8910503/878af5134147/ijms-23-02701-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e88/8910503/56ebcb3ed25b/ijms-23-02701-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e88/8910503/878af5134147/ijms-23-02701-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e88/8910503/56ebcb3ed25b/ijms-23-02701-g002.jpg

相似文献

1
Age Related Osteoporosis: Targeting Cellular Senescence.与年龄相关的骨质疏松症:靶向细胞衰老。
Int J Mol Sci. 2022 Feb 28;23(5):2701. doi: 10.3390/ijms23052701.
2
Inhibiting Cellular Senescence: A New Therapeutic Paradigm for Age-Related Osteoporosis.抑制细胞衰老:与年龄相关的骨质疏松症的一种新治疗范例。
J Clin Endocrinol Metab. 2018 Apr 1;103(4):1282-1290. doi: 10.1210/jc.2017-02694.
3
Senile Osteoporosis: The Involvement of Differentiation and Senescence of Bone Marrow Stromal Cells.老年性骨质疏松症:骨髓基质细胞分化和衰老的参与。
Int J Mol Sci. 2020 Jan 5;21(1):349. doi: 10.3390/ijms21010349.
4
Independent Roles of Estrogen Deficiency and Cellular Senescence in the Pathogenesis of Osteoporosis: Evidence in Young Adult Mice and Older Humans.雌激素缺乏和细胞衰老在骨质疏松症发病机制中的独立作用:在年轻成年小鼠和老年人类中的证据。
J Bone Miner Res. 2019 Aug;34(8):1407-1418. doi: 10.1002/jbmr.3729. Epub 2019 Jun 21.
5
The role of cellular senescence in diabetes mellitus and osteoporosis: molecular pathways and potential interventions.细胞衰老在糖尿病和骨质疏松症中的作用:分子途径和潜在干预措施。
Hormones (Athens). 2019 Dec;18(4):339-351. doi: 10.1007/s42000-019-00132-6. Epub 2019 Nov 8.
6
Cellular senescence in skeletal disease: mechanisms and treatment.骨骼疾病中的细胞衰老:机制与治疗。
Cell Mol Biol Lett. 2023 Oct 27;28(1):88. doi: 10.1186/s11658-023-00501-5.
7
Skeletal Aging and Osteoporosis: Mechanisms and Therapeutics.骨骼衰老与骨质疏松症:机制与治疗。
Int J Mol Sci. 2021 Mar 29;22(7):3553. doi: 10.3390/ijms22073553.
8
Targeting Cell Senescence for the Treatment of Age-Related Bone Loss.靶向细胞衰老治疗与年龄相关的骨质流失。
Curr Osteoporos Rep. 2019 Apr;17(2):70-85. doi: 10.1007/s11914-019-00504-2.
9
Mitochondria and cellular senescence: Implications for musculoskeletal ageing.线粒体与细胞衰老:对肌肉骨骼衰老的影响。
Free Radic Biol Med. 2019 Feb 20;132:3-10. doi: 10.1016/j.freeradbiomed.2018.10.417. Epub 2018 Oct 15.
10
Age-related alterations and senescence of mesenchymal stromal cells: Implications for regenerative treatments of bones and joints.间质基质细胞的衰老与年龄相关:对骨骼和关节再生治疗的影响。
Mech Ageing Dev. 2021 Sep;198:111539. doi: 10.1016/j.mad.2021.111539. Epub 2021 Jul 7.

引用本文的文献

1
Identification and validation of the cellular senescence-associated molecular pattern and diagnostic markers for osteoporosis.骨质疏松症细胞衰老相关分子模式及诊断标志物的鉴定与验证
BMC Med Genomics. 2025 Sep 2;18(1):140. doi: 10.1186/s12920-025-02205-5.
2
The Role of Senolytics in Osteoporosis.衰老细胞溶解剂在骨质疏松症中的作用。
Biomolecules. 2025 Aug 16;15(8):1176. doi: 10.3390/biom15081176.
3
From molecular mechanism to plant intervention: the bidirectional regulation of inflammation and oxidative stress in bone aging.

本文引用的文献

1
UBE2E3 regulates cellular senescence and osteogenic differentiation of BMSCs during aging.UBE2E3在衰老过程中调节骨髓间充质干细胞的细胞衰老和成骨分化。
PeerJ. 2021 Nov 18;9:e12253. doi: 10.7717/peerj.12253. eCollection 2021.
2
Senescent cells suppress innate smooth muscle cell repair functions in atherosclerosis.衰老细胞抑制动脉粥样硬化中的固有平滑肌细胞修复功能。
Nat Aging. 2021 Aug;1(8):698-714. doi: 10.1038/s43587-021-00089-5. Epub 2021 Aug 2.
3
Pharmacologic Interventions for Fracture Risk Reduction in the Oldest Old: What Is the Evidence?
从分子机制到植物干预:骨衰老中炎症与氧化应激的双向调节
Front Endocrinol (Lausanne). 2025 Jul 9;16:1634580. doi: 10.3389/fendo.2025.1634580. eCollection 2025.
4
Inflammaging-Driven Osteoporosis: Is a Galectin-Targeted Approach Needed?炎症衰老驱动的骨质疏松症:是否需要靶向半乳糖凝集素的方法?
Int J Mol Sci. 2025 Jul 4;26(13):6473. doi: 10.3390/ijms26136473.
5
Animal models for age-related osteoporosis.年龄相关性骨质疏松症的动物模型
Gerontology. 2025 May 20:1-29. doi: 10.1159/000546107.
6
Ganoderic Acid A Prevented Osteoporosis by Modulating the PIK3CA/p-Akt/TWIST1 Signaling Pathway.灵芝酸A通过调节PIK3CA/p-Akt/TWIST1信号通路预防骨质疏松症。
Food Sci Nutr. 2025 Apr 14;13(4):e70177. doi: 10.1002/fsn3.70177. eCollection 2025 Apr.
7
Osteoporosis Evaluation by Radiofrequency Echographic Multispectrometry (REMS) in Primary Healthcare.基层医疗中通过射频超声多光谱测定法(REMS)评估骨质疏松症
Diagnostics (Basel). 2025 Mar 22;15(7):808. doi: 10.3390/diagnostics15070808.
8
Global knowledge mapping of receptor activator of nuclear factor kappa-B ligand in osteoporotic fractures: a bibliometric analysis (2001-2024).骨质疏松性骨折中核因子κB受体激活剂配体的全球知识图谱:一项文献计量分析(2001 - 2024年)
Front Mol Biosci. 2025 Mar 26;12:1545109. doi: 10.3389/fmolb.2025.1545109. eCollection 2025.
9
Development and evaluation of a machine learning model for osteoporosis risk prediction in Korean women.韩国女性骨质疏松症风险预测机器学习模型的开发与评估
BMC Womens Health. 2025 Mar 28;25(1):146. doi: 10.1186/s12905-025-03669-4.
10
Bone mineral density and sex hormone binding globulin as potential mediators of the causal effect of urolithiasis on osteoporosis risk: a Mendelian randomization.骨矿物质密度和性激素结合球蛋白作为尿石症对骨质疏松症风险因果效应的潜在中介因素:一项孟德尔随机化研究。
Front Endocrinol (Lausanne). 2025 Feb 26;16:1460682. doi: 10.3389/fendo.2025.1460682. eCollection 2025.
降低高龄老人骨折风险的药物干预措施:证据有哪些?
JBMR Plus. 2021 Sep 5;5(10):e10538. doi: 10.1002/jbm4.10538. eCollection 2021 Oct.
4
Long noncoding RNA ZFAS1 suppresses osteogenic differentiation of bone marrow-derived mesenchymal stem cells by upregulating miR-499-EPHA5 axis.长链非编码 RNA ZFAS1 通过上调 miR-499-EPHA5 轴抑制骨髓间充质干细胞的成骨分化。
Mol Cell Endocrinol. 2022 Jan 1;539:111490. doi: 10.1016/j.mce.2021.111490. Epub 2021 Oct 13.
5
Modulation of fracture healing by the transient accumulation of senescent cells.衰老细胞的短暂积累对骨折愈合的调节作用。
Elife. 2021 Oct 7;10:e69958. doi: 10.7554/eLife.69958.
6
Senescent immune cells release grancalcin to promote skeletal aging.衰老免疫细胞释放粒酶来促进骨骼衰老。
Cell Metab. 2021 Oct 5;33(10):1957-1973.e6. doi: 10.1016/j.cmet.2021.08.009. Epub 2021 Sep 9.
7
Exercise to Mend Aged-tissue Crosstalk in Bone Targeting Osteoporosis & Osteoarthritis.运动修复靶向骨质疏松症和骨关节炎的组织老化对话。
Semin Cell Dev Biol. 2022 Mar;123:22-35. doi: 10.1016/j.semcdb.2021.08.011. Epub 2021 Sep 4.
8
Coating Polyelectrolyte Multilayers Loaded with Quercetin on Titanium Surfaces by Layer-By-Layer Assembly Technique to Improve Surface Osteogenesis Under Osteoporotic Condition.通过层层组装技术在钛表面涂覆载有槲皮素的聚电解质多层膜,以改善骨质疏松条件下的表面成骨作用。
J Biomed Nanotechnol. 2021 Jul 1;17(7):1392-1403. doi: 10.1166/jbn.2021.3115.
9
MicroRNA-29a Mitigates Osteoblast Senescence and Counteracts Bone Loss through Oxidation Resistance-1 Control of FoxO3 Methylation.微小RNA-29a通过调控氧化应激抗性-1介导的FoxO3甲基化减轻成骨细胞衰老并对抗骨质流失。
Antioxidants (Basel). 2021 Aug 4;10(8):1248. doi: 10.3390/antiox10081248.
10
Fisetin promotes osteoblast differentiation and osteogenesis through GSK-3β phosphorylation at Ser9 and consequent β-catenin activation, inhibiting osteoporosis.非瑟酮通过 GSK-3β 在 Ser9 的磷酸化和随后的β-连环蛋白激活促进成骨细胞分化和骨生成,从而抑制骨质疏松症。
Biochem Pharmacol. 2021 Oct;192:114676. doi: 10.1016/j.bcp.2021.114676. Epub 2021 Jul 10.