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了解微小RNA(miRNA)在骨质疏松症中的作用和机制的研究进展。

Progress in understanding the role and mechanism of miRNAs in osteoporosis.

作者信息

Meng Feifei, Yang Changwei, Li Na, Wang Huaxin

机构信息

Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.

College of First Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.

出版信息

Front Endocrinol (Lausanne). 2025 Aug 19;16:1544944. doi: 10.3389/fendo.2025.1544944. eCollection 2025.

Abstract

Please confirm that the below Frontiers AI generated Alt-Text is an accurate visual description of your Figure(s). These Figure Alt-text proposals won't replace your figure captions and will not be visible on your article. If you wish to make any changes, kindly provide the exact revised Alt-Text you would like to use, ensuring that the word-count remains at approximately 100 words for best accessibility results. Further information on Alt-Text can be found here.Osteoporosis is a systemic metabolic disorder characterized by compromised bone strength and increased fracture risk. Exosomes, extracellular vesicles measuring 40-160 nm in diameter, are critical mediators of intercellular communication. Among their bioactive components, microRNAs (miRNAs) have garnered attention for their role in the pathogenesis of Osteoporosis. Through complementary binding to the 3' untranslated regions of target genes, miRNAs regulate key processes such as bone formation, bone resorption, angiogenesis, and bone immunity. This review provides a comprehensive summary of the regulatory roles and underlying mechanisms of miRNAs in osteoporosis, offering insights into potential therapeutic strategies.

摘要

请确认以下由前沿人工智能生成的替代文本是否是对你的图的准确视觉描述。这些图的替代文本建议不会取代你的图注,并且在你的文章中不可见。如果你希望进行任何更改,请提供你想要使用的确切修订替代文本,确保字数保持在约100字以获得最佳可访问性结果。关于替代文本的更多信息可在此处找到。骨质疏松症是一种全身性代谢紊乱,其特征是骨强度受损和骨折风险增加。外泌体是直径为40 - 160纳米的细胞外囊泡,是细胞间通讯的关键介质。在其生物活性成分中,微小RNA(miRNA)因其在骨质疏松症发病机制中的作用而受到关注。通过与靶基因的3'非翻译区互补结合,miRNA调节骨形成、骨吸收、血管生成和骨免疫等关键过程。本综述全面总结了miRNA在骨质疏松症中的调节作用及潜在机制,为潜在治疗策略提供见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cd3/12401710/f50b74ad5b19/fendo-16-1544944-g001.jpg

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