Inter-university Laboratory of Human Movement Biology, Université de Lyon, University Jean Monnet Saint-Etienne, Saint-Étienne, France.
J Cachexia Sarcopenia Muscle. 2021 Apr;12(2):252-273. doi: 10.1002/jcsm.12678. Epub 2021 Mar 30.
Cancer cachexia is a complex multi-organ catabolic syndrome that reduces mobility, increases fatigue, decreases the efficiency of therapeutic strategies, diminishes the quality of life, and increases the mortality of cancer patients. This review provides an exhaustive and comprehensive analysis of cancer cachexia-related phenotypic changes in skeletal muscle at both the cellular and subcellular levels in human cancer patients, as well as in animal models of cancer cachexia. Cancer cachexia is characterized by a major decrease in skeletal muscle mass in human and animals that depends on the severity of the disease/model and the localization of the tumour. It affects both type 1 and type 2 muscle fibres, even if some animal studies suggest that type 2 muscle fibres would be more prone to atrophy. Animal studies indicate an impairment in mitochondrial oxidative metabolism resulting from a decrease in mitochondrial content, an alteration in mitochondria morphology, and a reduction in mitochondrial metabolic fluxes. Immuno-histological analyses in human and animal models also suggest that a faulty mechanism of skeletal muscle repair would contribute to muscle mass loss. An increase in collagen deposit, an accumulation of fat depot outside and inside the muscle fibre, and a disrupted contractile machinery structure are also phenotypic features that have been consistently reported in cachectic skeletal muscle. Muscle function is also profoundly altered during cancer cachexia with a strong reduction in skeletal muscle force. Even though the loss of skeletal muscle mass largely contributes to the loss of muscle function, other factors such as muscle-nerve interaction and calcium handling are probably involved in the decrease in muscle force. Longitudinal analyses of skeletal muscle mass by imaging technics and skeletal muscle force in cancer patients, but also in animal models of cancer cachexia, are necessary to determine the respective kinetics and functional involvements of these factors. Our analysis also emphasizes that measuring skeletal muscle force through standardized tests could provide a simple and robust mean to early diagnose cachexia in cancer patients. That would be of great benefit to cancer patient's quality of life and health care systems.
癌症恶病质是一种复杂的多器官消耗综合征,它降低了患者的活动能力,增加了疲劳感,降低了治疗策略的效率,降低了生活质量,并增加了癌症患者的死亡率。这篇综述全面分析了人类癌症患者和癌症恶病质动物模型中骨骼肌在细胞和亚细胞水平上与癌症恶病质相关的表型变化。癌症恶病质的特征是骨骼肌质量的大量减少,这取决于疾病/模型的严重程度和肿瘤的位置。它影响到 1 型和 2 型肌肉纤维,尽管一些动物研究表明 2 型肌肉纤维更容易萎缩。动物研究表明,线粒体氧化代谢受损是由于线粒体含量减少、线粒体形态改变和线粒体代谢通量减少所致。人类和动物模型的免疫组织化学分析也表明,骨骼肌修复的机制失灵会导致肌肉质量的丧失。胶原蛋白沉积的增加、肌肉纤维内外脂肪库的积累以及收缩机制结构的破坏也是恶病质骨骼肌的一致表型特征。肌肉功能在癌症恶病质期间也受到严重影响,骨骼肌力量明显下降。尽管骨骼肌质量的丧失在很大程度上导致了肌肉功能的丧失,但其他因素,如肌肉-神经相互作用和钙处理,可能也参与了肌肉力量的下降。通过影像学技术对癌症患者的骨骼肌质量进行纵向分析,以及对癌症恶病质动物模型的骨骼肌力量进行纵向分析,有助于确定这些因素的各自动力学和功能相关性。我们的分析还强调,通过标准化测试测量骨骼肌力量可以提供一种简单而可靠的方法,以便早期诊断癌症患者的恶病质。这将对癌症患者的生活质量和医疗保健系统有很大的好处。