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TNF-alpha and cancer cachexia: Molecular insights and clinical implications

机译:TNF-α和癌症恶毒糖尿病:分子见解和临床意义

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Cancer cachexia characterized by a chronic wasting syndrome, involves skeletal muscle loss and adipose tissue loss and resistance to conventional nutritional support. Cachexia is responsible for the reduction in quality and length of life of cancer patients. It also decreases the muscle strength of the patients. The pro-inflammatory and pro-cachectic factors produced by the tumor cells have important role in genesis of cachexia. A number of pro-inflammatory cytokines, like interleukin-1 (IL-1), IL-6, tumor necrosis factor- alpha (TNF-alpha) may have important role in the pathological mechanisms of cachexia in cancer. Particularly, TNF-alpha has a direct catabolic effect on skeletal muscle and causes wasting of muscle by the induction of the ubiquitin-proteasome system (UPS). In cancer cachexia condition, there is alteration in carbohydrate, protein and fat metabolism. TNF-alpha is responsible for the increase in gluconeogenesis, loss of adipose tissue and proteolysis, while causing decrease in protein, lipid and glycogen synthesis. It has been associated with the formation of IL-1 and increases the uncoupling protein-2 (UCP2) and UCP3 expression in skeletal muscle in cachectic state. The main aim of the present review is to evaluate and discuss the role of TNF-alpha in different metabolic alterations and muscle wasting in cancer cachexia. (C) 2016 Elsevier Inc. All rights reserved.
机译:癌症恶化以慢性浪费综合征为特征,涉及骨骼肌损失和脂肪组织丧失和对常规营养载体的抵抗力。 Cachexia负责降低癌症患者的寿命的质量和长度。它还降低患者的肌肉力量。由肿瘤细胞产生的促炎和亲谱因子在恶毒症的成因中具有重要作用。许多促炎细胞因子,如白细胞介素-1(IL-1),IL-6,肿瘤坏死因子 - α(TNF-alpha)可能在癌症恶病症的病理机制中具有重要作用。特别是,TNF-α对骨骼肌具有直接的分解代谢作用,并通过诱导泛素 - 蛋白酶体系(UPS)诱导肌肉浪费。在癌症恶毒症病症中,有碳水化合物,蛋白质和脂肪代谢的变化。 TNF-α负责葡糖生成增加,脂肪组织和蛋白水解的损失,同时导致蛋白质,脂质和糖原合成的降低。它已与IL-1的形成有关,并在骨颈肌肉中增加骨折蛋白-2(UCP2)和UCP3表达中的骨科肌肉。本综述的主要目的是评估和讨论TNF-α在癌症恶病症中不同代谢改变和肌肉萎缩的作用。 (c)2016 Elsevier Inc.保留所有权利。

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