Anti-inflammatory therapies in cancer cachexia

被引:60
|
作者
Argiles, Josep M. [1 ]
Busquets, Silvia
Lopez-Soriano, Francisco J.
机构
[1] Univ Barcelona, Fac Biol, Canc Res Grp, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain
关键词
Cachexia; Inflammation; Muscle wasting; NECROSIS-FACTOR-ALPHA; TUMOR-BEARING RATS; CHAIN AMINO-ACIDS; EICOSAPENTAENOIC ACID; PARENTERAL-NUTRITION; SKELETAL-MUSCLE; DOUBLE-BLIND; CELL-PROLIFERATION; MURINE MODEL; BODY-WEIGHT;
D O I
10.1016/j.ejphar.2011.07.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Disease progression in cancer is dependent on the complex interaction between the tumor and the host inflammatory response. Indeed, both the tumor and the patient produce cytokines that act on multiple target sites such as bone marrow, myocytes. hepatocytes, adipocytes, endothelial cells and neurons, where they produce a complex cascade of biological responses leading to the wasting associated with cachexia. The cytokines that have been involved in this cachectic response are TNF-alpha, IL-1, IL-6 and interferon-gamma. Interestingly, these cytokines share the same metabolic effects and their activities are closely interrelated. In many cases these cytokines exhibit synergic effects when administered together. Therefore, therapeutic strategies - either nutritional or pharmacological - have been based on either blocking their synthesis or their action. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:S81 / S86
页数:6
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