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癌症恶病质及相关代谢功能障碍

Cancer Cachexia and Related Metabolic Dysfunction.

机构信息

Heart Institute (InCor), University of São Paulo Medical School, São Paulo SP 05403-900, Brazil.

Department of Cardiology and Pneumology, University Medicine Göttingen (UMG), DE-37075 Goettingen, Germany.

出版信息

Int J Mol Sci. 2020 Mar 27;21(7):2321. doi: 10.3390/ijms21072321.

Abstract

Cancer cachexia is a complex multifactorial syndrome marked by a continuous depletion of skeletal muscle mass associated, in some cases, with a reduction in fat mass. It is irreversible by nutritional support alone and affects up to 74% of patients with cancer-dependent on the underlying type of cancer-and is associated with physical function impairment, reduced response to cancer-related therapy, and higher mortality. Organs, like muscle, adipose tissue, and liver, play an important role in the progression of cancer cachexia by exacerbating the pro- and anti-inflammatory response initially activated by the tumor and the immune system of the host. Moreover, this metabolic dysfunction is produced by alterations in glucose, lipids, and protein metabolism that, when maintained chronically, may lead to the loss of skeletal muscle and adipose tissue. Although a couple of drugs have yielded positive results in increasing lean body mass with limited impact on physical function, a single therapy has not lead to effective treatment of this condition. Therefore, a multimodal intervention, including pharmacological agents, nutritional support, and physical exercise, may be a reasonable approach for future studies to better understand and prevent the wasting of body compartments in patients with cancer cachexia.

摘要

癌症恶病质是一种复杂的多因素综合征,其特征是骨骼肌持续消耗,在某些情况下,还伴有脂肪量减少。仅靠营养支持是无法逆转的,并且影响到高达 74%的癌症患者——具体取决于潜在的癌症类型——并与身体功能障碍、对癌症相关治疗的反应降低和更高的死亡率有关。肌肉、脂肪组织和肝脏等器官通过加剧最初由肿瘤和宿主免疫系统激活的促炎和抗炎反应,在癌症恶病质的进展中起着重要作用。此外,这种代谢功能障碍是由葡萄糖、脂质和蛋白质代谢的改变引起的,当这些改变持续存在时,可能导致骨骼肌和脂肪组织的丧失。尽管有几种药物在增加瘦体重方面取得了积极的结果,但对身体功能的影响有限,单一疗法尚未有效治疗这种疾病。因此,包括药物治疗、营养支持和体育锻炼在内的多模式干预可能是未来研究的合理方法,以更好地理解和预防癌症恶病质患者身体各部位的消耗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/643e/7177950/fa7e25ec9981/ijms-21-02321-g001.jpg

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