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线粒体自噬在骨关节炎中的作用。

The role of mitochondrial autophagy in osteoarthritis.

作者信息

Wang Genchun, Zhang Xiong, Xu Jingting, Hou Liangcai, Guo Zhou, Sun Kai, Guo Fengjing

机构信息

Department of Orthopedics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, China.

Orthopedic Medical Center, Union Hospital, Fujian Medical University, Fuzhou, Fujian 350000, China.

出版信息

iScience. 2024 Aug 15;27(9):110741. doi: 10.1016/j.isci.2024.110741. eCollection 2024 Sep 20.

Abstract

Osteoarthritis (OA) is a progressive degenerative joint disease, and the underlying molecular mechanisms of OA remain poorly understood. This study aimed to elucidate the relationship between mitochondrial autophagy and OA by identifying key regulatory genes and their biological functions. Utilizing bioinformatics analyses of RNA expression profiles from the GSE55235 dataset, we identified 2,136 differentially expressed genes, leading to the discovery of hub genes associated with mitochondrial autophagy and OA. Gene set enrichment analysis (GSEA) revealed their involvement in critical pathways, highlighting their potential roles in OA pathogenesis. Furthermore, our study explored the immunological landscape of OA, identifying distinct immune cell infiltration patterns that contribute to the disease's inflammatory profile. We also evaluated the therapeutic potential of drugs targeting these hub genes, suggesting potential approaches for OA treatment. Collectively, this study advances our knowledge of mitochondrial autophagy in OA and proposes promising biomarkers and therapeutic targets.

摘要

骨关节炎(OA)是一种进行性退行性关节疾病,而OA的潜在分子机制仍知之甚少。本研究旨在通过鉴定关键调控基因及其生物学功能来阐明线粒体自噬与OA之间的关系。利用来自GSE55235数据集的RNA表达谱进行生物信息学分析,我们鉴定出2136个差异表达基因,从而发现了与线粒体自噬和OA相关的枢纽基因。基因集富集分析(GSEA)揭示了它们参与关键途径,突出了它们在OA发病机制中的潜在作用。此外,我们的研究探索了OA的免疫格局,确定了导致该疾病炎症特征的独特免疫细胞浸润模式。我们还评估了靶向这些枢纽基因的药物的治疗潜力,提出了OA治疗的潜在方法。总的来说,本研究推进了我们对OA中线粒体自噬的认识,并提出了有前景的生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09c6/11402317/1c86c921d38c/fx1.jpg

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