Department of Orthopaedics, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, China.
Department of Sports Medicine, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, China; School of Medicine, Guangxi University of Chinese Medicine, Nanning, China.
Am J Pathol. 2022 Dec;192(12):1648-1657. doi: 10.1016/j.ajpath.2022.09.003. Epub 2022 Sep 27.
Skeletal muscle atrophy is the consequence of protein degradation exceeding protein synthesis because of disease, aging, and physical inactivity. Patients with skeletal muscle atrophy have decreased muscle mass and fiber cross-sectional area, and experience reduced survival quality and motor function. The forkhead box O (FOXO) signaling pathway plays an important role in the pathogenesis of skeletal muscle atrophy by regulating E3 ubiquitin ligases and some autophagy factors. However, the mechanism of FOXO signaling pathway leading to skeletal muscle atrophy is still unclear. The development of treatment strategies for skeletal muscle atrophy has been a thorny clinical problem. FOXO-targeted therapy to treat skeletal muscle atrophy is a promising approach, and an increasing number of relevant studies have been reported. This article reviews the mechanism and therapeutic targets of the FOXO signaling pathway mediating skeletal muscle atrophy, and provides ideas for the clinical treatment of this condition.
骨骼肌萎缩是由于疾病、衰老和身体活动减少导致蛋白质降解超过蛋白质合成的结果。患有骨骼肌萎缩的患者肌肉质量和纤维横截面积减少,生存质量和运动功能降低。叉头框 O(FOXO)信号通路通过调节 E3 泛素连接酶和一些自噬因子在骨骼肌萎缩的发病机制中发挥重要作用。然而,FOXO 信号通路导致骨骼肌萎缩的机制尚不清楚。骨骼肌萎缩治疗策略的发展一直是一个棘手的临床问题。针对 FOXO 治疗骨骼肌萎缩是一种很有前途的方法,并且已经有越来越多的相关研究报告。本文综述了 FOXO 信号通路介导骨骼肌萎缩的机制和治疗靶点,为该疾病的临床治疗提供了思路。