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硬化蛋白在骨疾病中的作用。

The Role of Sclerostin in Bone Diseases.

作者信息

Vasiliadis Elias S, Evangelopoulos Dimitrios-Stergios, Kaspiris Angelos, Benetos Ioannis S, Vlachos Christos, Pneumaticos Spyros G

机构信息

3rd Department of Orthopaedics, School of Medicine, National and Kapodistrian University of Athens, KAT Hospital, 16541 Athens, Greece.

Laboratory of Molecular Pharmacology, Division for Orthopaedic Research, School of Health Sciences, University of Patras, 26504 Rion, Greece.

出版信息

J Clin Med. 2022 Feb 2;11(3):806. doi: 10.3390/jcm11030806.

DOI:10.3390/jcm11030806
PMID:35160258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8836457/
Abstract

Sclerostin has been identified as an important regulator of bone homeostasis through inhibition of the canonical Wnt-signaling pathway, and it is involved in the pathogenesis of many different skeletal diseases. Many studies have been published in the last few years regarding sclerostin's origin, regulation, and mechanism of action. The ongoing research emphasizes the potential therapeutic implications of sclerostin in many pathological conditions with or without skeletal involvement. Antisclerostin antibodies have recently been approved for the treatment of osteoporosis, and several animal studies and clinical trials are currently under way to evaluate the effectiveness of antisclerostin antibodies in the treatment of other than osteoporosis skeletal disorders and cancer with promising results. Understanding the exact role of sclerostin may lead to new therapeutic approaches for the treatment of skeletal disorders.

摘要

硬化素已被确定为通过抑制经典Wnt信号通路来调节骨稳态的重要因子,并且它参与了许多不同骨骼疾病的发病机制。在过去几年中,已经发表了许多关于硬化素的起源、调节及其作用机制的研究。正在进行的研究强调了硬化素在许多有或没有骨骼受累的病理状况中的潜在治疗意义。抗硬化素抗体最近已被批准用于治疗骨质疏松症,目前正在进行多项动物研究和临床试验,以评估抗硬化素抗体在治疗除骨质疏松症之外的骨骼疾病和癌症方面的有效性,结果令人鼓舞。了解硬化素的确切作用可能会带来治疗骨骼疾病的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8691/8836457/c820c0b4ccc9/jcm-11-00806-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8691/8836457/80756a7462e8/jcm-11-00806-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8691/8836457/c820c0b4ccc9/jcm-11-00806-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8691/8836457/80756a7462e8/jcm-11-00806-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8691/8836457/c820c0b4ccc9/jcm-11-00806-g002.jpg

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Endocr Connect. 2019 Jul;8(7):923-934. doi: 10.1530/EC-19-0104.
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Osteoimmunology: evolving concepts in bone-immune interactions in health and disease.骨免疫学:健康与疾病中骨-免疫相互作用的新概念。
Nat Rev Immunol. 2019 Oct;19(10):626-642. doi: 10.1038/s41577-019-0178-8. Epub 2019 Jun 11.
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Modulation of the Wnt pathway through inhibition of CLK2 and DYRK1A by lorecivivint as a novel, potentially disease-modifying approach for knee osteoarthritis treatment.
棕榈生育三烯酚可维持去卵巢大鼠的小梁骨细胞指数并调节骨细胞标志物的表达。
Biomedicines. 2025 May 18;13(5):1220. doi: 10.3390/biomedicines13051220.
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Leveraging Nanoscience and Strategic Delivery for the Expedition of Osteoporosis.利用纳米科学与战略交付推动骨质疏松症研究进展
AAPS PharmSciTech. 2025 May 9;26(5):129. doi: 10.1208/s12249-025-03120-9.
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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.
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The Crosstalk Between Cartilage and Bone in Skeletal Growth.骨骼生长过程中软骨与骨之间的相互作用
Biomedicines. 2024 Nov 21;12(12):2662. doi: 10.3390/biomedicines12122662.
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Sclerostin as a new target of diabetes-induced osteoporosis.硬化蛋白作为糖尿病性骨质疏松症的新靶点。
Front Endocrinol (Lausanne). 2024 Dec 10;15:1491066. doi: 10.3389/fendo.2024.1491066. eCollection 2024.
8
Sclerostin as a Genetic Determinant of Trabecular Bone Score in Postmenopausal Women: The Bushehr Elderly Health (BEH) Program.硬化蛋白作为绝经后女性小梁骨评分的遗传决定因素:布什尔老年健康(BEH)项目
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通过抑制 CLK2 和 DYRK1A 来调节 Wnt 通路,这是一种治疗膝骨关节炎的新的、潜在的疾病修饰方法,洛塞维文特(lorecivivint)为此提供了可能。
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J Bone Miner Res. 2019 Jan;34(1):171-181. doi: 10.1002/jbmr.3581. Epub 2018 Sep 24.
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J Clin Endocrinol Metab. 2018 Sep 1;103(9):3183-3193. doi: 10.1210/jc.2017-02163.
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JCI Insight. 2018 Jun 7;3(11). doi: 10.1172/jci.insight.98673.
10
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Int Orthop. 2018 Jul;42(7):1675-1682. doi: 10.1007/s00264-018-3979-7. Epub 2018 May 21.