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《骨关节炎的遗传学和功能基因组学》。

The Genetics and Functional Genomics of Osteoarthritis.

机构信息

Graduate School of Experimental Medicine, TUM School of Medicine and Health, Technical University of Munich, Munich, Germany.

Institute of Translational Genomics, Helmholtz Munich, Neuherberg, Germany; email:

出版信息

Annu Rev Genomics Hum Genet. 2024 Aug;25(1):239-257. doi: 10.1146/annurev-genom-010423-095636.

Abstract

Osteoarthritis is the most prevalent whole-joint degenerative disorder, and is characterized by the degradation of articular cartilage and the underlying bone structures. Almost 600 million people are affected by osteoarthritis worldwide. No curative treatments are available, and management strategies focus mostly on pain relief. Here, we provide a comprehensive overview of the available human genetic and functional genomics studies for osteoarthritis to date and delineate how these studies have helped shed light on disease etiopathology. We highlight genetic discoveries from genome-wide association studies and provide a detailed overview of molecular-level investigations in osteoarthritis tissues, including methylation-, transcriptomics-, and proteomics-level analyses. We review how functional genomics data from different molecular levels have helped to prioritize effector genes that can be used as drug targets or drug-repurposing opportunities. Finally, we discuss future directions with the potential to drive a step change in osteoarthritis research.

摘要

骨关节炎是最常见的全关节退行性疾病,其特征是关节软骨和下面的骨结构退化。全世界有近 6 亿人受骨关节炎影响。目前尚无有效的治疗方法,治疗策略主要集中在缓解疼痛上。在这里,我们全面概述了迄今为止已有的针对骨关节炎的人类遗传和功能基因组学研究,并阐明了这些研究如何帮助揭示疾病的病因病理。我们重点介绍了全基因组关联研究中的遗传发现,并详细概述了骨关节炎组织中的分子水平研究,包括甲基化、转录组学和蛋白质组学分析。我们回顾了来自不同分子水平的功能基因组学数据如何有助于确定可作为药物靶点或药物再利用机会的效应基因。最后,我们讨论了具有推动骨关节炎研究取得重大进展潜力的未来方向。

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