Muscle wasting: An overview of recent developments in basic research

被引:29
作者
Palus, Sandra [1 ]
von Haehling, Stephan [1 ]
Springer, Jochen [1 ,2 ]
机构
[1] Univ Med Ctr Gottingen, Dept Innovat Clin Trials, D-37075 Gottingen, Germany
[2] Univ Med Ctr Gottingen, Dept Cardiol & Pneumol, D-37075 Gottingen, Germany
关键词
Cachexia; Muscle wasting; Signaling; Target; E3 UBIQUITIN LIGASE; HEART FAILURE MODEL; CREATINE POOL SIZE; GROWTH-FACTOR; SKELETAL-MUSCLE; CANCER CACHEXIA; SIGNALING PATHWAYS; BODY-COMPOSITION; ACTRIIB ANTAGONISM; INSULIN-RESISTANCE;
D O I
10.1016/j.ijcard.2014.08.086
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The syndrome of cachexia, i.e, involuntary weight loss in patients with underlying diseases, sarcopenia, i.e, loss of muscle mass due to ageing, and general muscle atrophy from disuse and/or prolonged bed rest have received more attention over the last decades. All lead to a higher morbidity and mortality in patients and therefore, they represent a major socio-economic burden for the society today. This mini-review looks at recent developments in basic research that are relevant to the loss of skeletal muscle. It aims to cover the most significant publication of last three years on the causes and effects of muscle wasting, new targets for therapy development and potential biomarkers for assessing skeletal muscle mass. The targets include 1) E-3 ligases: TRIM32, SOCS1 and SOCS3 by involving the elongin BC ubiquitin-ligase, Cbl-b, culling 7, Fbx040, MG53 (TRIM72) and the mitochondrial Mull, 2) the kinase MST1 and 3) the G-protein G alpha i(2) D(3)-creatine has the potential to be used as a novel biomarker that allows to monitor actual change in skeletal muscle mass over time. In conclusion, significant development efforts are being made by academic groups as well as numerous pharmaceutical companies to identify new targets and biomarkers muscle, as muscle wasting represents a great medical need, but no therapies have been approved in the last decades. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:640 / 644
页数:5
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