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癌症恶病质与糖尿病:代谢改变的相似性及可能的治疗方法

Cancer cachexia and diabetes: similarities in metabolic alterations and possible treatment.

作者信息

Chevalier Stéphanie, Farsijani Samaneh

机构信息

a Department of Medicine and School of Dietetics and Human Nutrition, Crabtree Nutrition Laboratories, McGill University Health Centre-Royal Victoria Hospital, 687 ave des Pins Ouest, room H6.61, Montreal, QC H3A 1A1, Canada.

出版信息

Appl Physiol Nutr Metab. 2014 Jun;39(6):643-53. doi: 10.1139/apnm-2013-0369. Epub 2013 Nov 11.

Abstract

Cancer cachexia is a metabolic syndrome featuring many alterations typical of type 2 diabetes (T2D). While muscle wasting is a hallmark of cachexia, epidemiological evidence also supports an accelerated age-related muscle loss in T2D. Insulin resistance manifests in both conditions and impairs glucose disposal and protein anabolism by tissues. A greater contribution of gluconeogenesis to glucose production may limit amino acid availability for muscle protein synthesis, further aggravating muscle loss. In the context of inter-dependence between glucose and protein metabolism, the present review summarizes the current state of knowledge on alterations that may lead to muscle wasting in human cancer. By highlighting the similarities with T2D, a disease that has been more extensively studied, the objective of this review is to provide a better understanding of the pathophysiology of cancer cachexia and to consider potential treatments usually targeted for T2D. Nutritional approaches aimed at stimulating protein anabolism might include specially formulated food with optimal protein and amino acid composition. Because the gradual muscle loss in T2D may be attenuated by diabetes treatment, anti-diabetic drugs might be considered in cachexia treatment. Metformin emerges as a choice candidate as it acts both on reducing gluconeogenesis and improving insulin sensitivity, and has demonstrated tumour suppressor properties in multiple cancer types. Such a multimodal approach to slow or reverse muscle wasting in cachexia warrants further investigation.

摘要

癌症恶病质是一种代谢综合征,具有许多2型糖尿病(T2D)的典型改变。虽然肌肉萎缩是恶病质的一个标志,但流行病学证据也支持T2D患者与年龄相关的肌肉流失加速。胰岛素抵抗在这两种情况下均有表现,并损害组织的葡萄糖处理和蛋白质合成代谢。糖异生对葡萄糖生成的更大贡献可能会限制肌肉蛋白质合成所需的氨基酸供应,进一步加重肌肉流失。在葡萄糖和蛋白质代谢相互依存的背景下,本综述总结了目前关于可能导致人类癌症患者肌肉萎缩的改变的知识现状。通过强调与T2D(一种已得到更广泛研究的疾病)的相似性,本综述的目的是更好地理解癌症恶病质的病理生理学,并考虑通常针对T2D的潜在治疗方法。旨在刺激蛋白质合成代谢的营养方法可能包括具有最佳蛋白质和氨基酸组成的特殊配方食品。由于糖尿病治疗可能会减轻T2D患者逐渐出现的肌肉流失,因此在恶病质治疗中可能会考虑使用抗糖尿病药物。二甲双胍成为一个选择候选药物,因为它既可以减少糖异生又可以提高胰岛素敏感性,并且在多种癌症类型中已显示出肿瘤抑制特性。这种减缓或逆转恶病质中肌肉萎缩的多模式方法值得进一步研究。

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