MOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.
Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.
Biochem J. 2021 May 14;478(9):1663-1688. doi: 10.1042/BCJ20201009.
Cancer cachexia often occurs in malignant tumors and is a multifactorial and complex symptom characterized by wasting of skeletal muscle and adipose tissue, resulting in weight loss, poor life quality and shorter survival. The pathogenic mechanism of cancer cachexia is complex, involving a variety of molecular substrates and signal pathways. Advancements in understanding the molecular mechanisms of cancer cachexia have provided a platform for the development of new targeted therapies. Although recent outcomes of early-phase trials have showed that several drugs presented an ideal curative effect, monotherapy cannot be entirely satisfactory in the treatment of cachexia-associated symptoms due to its complex and multifactorial pathogenesis. Therefore, the lack of definitive therapeutic strategies for cancer cachexia emphasizes the need to develop a better understanding of the underlying mechanisms. Increasing evidences show that the progression of cachexia is associated with metabolic alternations, which mainly include excessive energy expenditure, increased proteolysis and mitochondrial dysfunction. In this review, we provided an overview of the key mechanisms of cancer cachexia, with a major focus on muscle atrophy, adipose tissue wasting, anorexia and fatigue and updated the latest progress of pharmacological management of cancer cachexia, thereby further advancing the interventions that can counteract cancer cachexia.
癌症恶病质常发生于恶性肿瘤,并以骨骼肌和脂肪组织减少为特征的多因素、复杂症状,导致体重减轻、生活质量差和生存期缩短。癌症恶病质的发病机制复杂,涉及多种分子底物和信号通路。对癌症恶病质分子机制的深入了解为新的靶向治疗的发展提供了平台。尽管最近早期试验的结果表明,几种药物表现出理想的疗效,但由于其发病机制复杂且多因素,单一疗法在治疗恶病质相关症状方面并不能完全令人满意。因此,癌症恶病质缺乏明确的治疗策略强调需要更好地了解潜在的机制。越来越多的证据表明,恶病质的进展与代谢改变有关,主要包括能量消耗过多、蛋白水解增加和线粒体功能障碍。在这篇综述中,我们概述了癌症恶病质的关键机制,主要集中在肌肉萎缩、脂肪组织减少、厌食和疲劳上,并更新了癌症恶病质药物治疗的最新进展,从而进一步推进对抗癌症恶病质的干预措施。