Molecular and neuroendocrine mechanisms of cancer cachexia

被引:60
作者
Mendes, Maria Carolina S. [1 ]
Pimentel, Gustavo D. [1 ]
Costa, Felipe O. [1 ]
Carvalheira, Jose B. C. [1 ]
机构
[1] State Univ Campinas UNICAMP, Dept Internal Med, Fac Med Sci, BR-13083970 Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
hypothalamus; cancer; muscle; neuropeptides; neuroendocrinology; TUMOR-BEARING RATS; LIPID-MOBILIZING FACTOR; SKELETAL-MUSCLE ATROPHY; NECROSIS-FACTOR-ALPHA; BROWN-ADIPOSE-TISSUE; ACTIVATED PROTEIN-KINASE; NF-KAPPA-B; MELANOCORTIN-4 RECEPTOR ANTAGONIST; PROTEOLYSIS-INDUCING FACTOR; AGOUTI-RELATED PEPTIDE;
D O I
10.1530/JOE-15-0170
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cancer and its morbidities, such as cancer cachexia, constitute a major public health problem. Although cancer cachexia has afflicted humanity for centuries, its underlying multifactorial and complex physiopathology has hindered the understanding of its mechanism. During the last few decades we have witnessed a dramatic increase in the understanding of cancer cachexia pathophysiology. Anorexia and muscle and adipose tissue wasting are the main features of cancer cachexia. These apparently independent symptoms have humoral factors secreted by the tumor as a common cause. Importantly, the hypothalamus has emerged as an organ that senses the peripheral signals emanating from the tumoral environment, and not only elicits anorexia but also contributes to the development of muscle and adipose tissue loss. Herein, we review the roles of factors secreted by the tumor and its effects on the hypothalamus, muscle and adipose tissue, as well as highlighting the key targets that are being exploited for cancer cachexia treatment.
引用
收藏
页码:R29 / R43
页数:15
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