叉头盒O3a (FOXO3a)在骨和软骨疾病中的作用

IF 5.1 2区 医学 Q1 CHEMISTRY, MEDICINAL Drug Design, Development and Therapy Pub Date : 2025-02-27 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S494841
Zhenyu Wu, Wang Zhan, Longhuo Wu, Luhu Yu, Xunlu Xie, Fang Yu, Weihao Kong, Shengrong Bi, Shiwei Liu, Guoqiang Yin, Jianguo Zhou
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引用次数: 0

摘要

骨和软骨疾病与肌肉骨骼残疾显著相关。然而,没有有效的药物可以治愈它们。FOXO3a是FOXO家族的一员,参与细胞增殖、ROS解毒、自噬和凋亡。FOXO3a的生物学功能可以通过磷酸化和乙酰化等翻译后修饰(PTMs)来调节。几种信号通路,如MAPK、NF-κB、PI3K/AKT和AMPK/Sirt1通路,通过介导FOXO3a的表达参与骨和软骨疾病的发生。特别是FOXO3a作为转录因子介导多种基因的表达,如MnSOD、CAT、BIM、BBC3、CDK6等。FOXO3a在骨和软骨的代谢中起关键作用。本文主要讨论FOXO3a在骨质疏松症(OP)、骨关节炎(OA)、类风湿关节炎(RA)、强直性脊柱炎(as)、椎间盘退变(IDD)等骨软骨疾病中的生物学功能。FOXO3a可促进成骨分化,诱导成骨细胞增殖,抑制破骨细胞活性,抑制软骨细胞凋亡,减轻炎症反应。综上所述,FOXO3a表达上调显示出有益的效果,FOXO3a已成为骨和软骨疾病的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Roles of Forkhead Box O3a (FOXO3a) in Bone and Cartilage Diseases - A Narrative Review.

Bone and cartilage diseases are significantly associated with musculoskeletal disability. However, no effective drugs are available to cure them. FOXO3a, a member of the FOXO family, has been implicated in cell proliferation, ROS detoxification, autophagy, and apoptosis. The biological functions of FOXO3a can be modulated by post-translational modifications (PTMs), such as phosphorylation and acetylation. Several signaling pathways, such as MAPK, NF-κB, PI3K/AKT, and AMPK/Sirt1 pathways, have been implicated in the development of bone and cartilage diseases by mediating the expression of FOXO3a. In particular, FOXO3a acts as a transcriptional factor in mediating the expression of various genes, such as MnSOD, CAT, BIM, BBC3, and CDK6. FOXO3a plays a critical role in the metabolism of bone and cartilage. In this article, we mainly discussed the biological functions of FOXO3a in bone and cartilage diseases, such as osteoporosis (OP), osteoarthritis (OA), rheumatoid arthritis (RA), ankylosing spondylitis (AS), and intervertebral disc degeneration (IDD). FOXO3a can promote osteogenic differentiation, induce osteoblast proliferation, inhibit osteoclast activity, suppress chondrocyte apoptosis, and reduce inflammatory responses. Collectively, up-regulation of FOXO3a expression shows beneficial effects, and FOXO3a has become a potential target for bone and cartilage diseases.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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