Tumour-derived PTH-related protein triggers adipose tissue browning and cancer cachexia

被引:560
作者
Kir, Serkan [1 ]
White, James P. [1 ]
Kleiner, Sandra [1 ]
Kazak, Lawrence [1 ]
Cohen, Paul [1 ]
Baracos, Vickie E. [2 ]
Spiegelman, Bruce M. [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02215 USA
[2] Univ Alberta, Div Palliat Care Med, Dept Oncol, Edmonton, AB T6G 1Z2, Canada
基金
美国国家卫生研究院;
关键词
HORMONE-RELATED PROTEIN; SKELETAL-MUSCLE; MONOCLONAL-ANTIBODY; NUDE-MICE; MECHANISMS; CELL; THERMOGENESIS; ACTIVATION; SURVIVAL;
D O I
10.1038/nature13528
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Cachexia is a wasting disorder of adipose and skeletal muscle tissues that leads to profound weight loss and frailty. About half of all cancer patients suffer from cachexia, which impairs quality of life, limits cancer therapy and decreases survival. One key characteristic of cachexia is higher resting energy expenditure levels than in healthy individuals, which has been linked to greater thermogenesis by brown fat(1-6). How tumours induce brown fat activity is unknown. Here, using a Lewis lung carcinoma model of cancer cachexia, we show that tumour-derived parathyroid-hormone-related protein (PTHrP) has an important role in wasting, through driving the expression of genes involved in thermogenesis in adipose tissues. Neutralization of PTHrP in tumour-bearing mice blocked adipose tissue browning and the loss of muscle mass and strength. Our results demonstrate that PTHrP mediates energy wasting in fat tissues and contributes to the broader aspects of cancer cachexia. Thus, neutralization of PTHrP might hold promise for ameliorating cancer cachexia and improving patient survival.
引用
收藏
页码:100 / +
页数:18
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