Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, Colorado, USA.
Cancer Res. 2011 Mar 1;71(5):1710-20. doi: 10.1158/0008-5472.CAN-10-3145. Epub 2010 Dec 16.
Approximately one-third of cancer deaths are caused by cachexia, a severe form of skeletal muscle and adipose tissue wasting that affects men more than women. The heart also undergoes atrophy in cancer patients, but the mechanisms and the basis for apparent sex differences are unclear. In a mouse colon-adenocarcinoma model, cancer causes a loss of cardiac mass due to a decrease in cardiac myocyte size that is associated with reduced levels of all sarcomeric proteins. Unlike skeletal muscle cachexia, atrophic hearts do not upregulate the ubiquitin-proteasome system or its activity but increase autophagy. Thus, cancer causes cardiac atrophy by a mechanism distinct from that in skeletal muscle. Male tumor-bearing mice have a more severe phenotype than females, including greater cardiac mass loss and mortality, a more robust pro-inflammatory response to the tumor, and greater cardiac autophagy. In females, estrogen protects against cancer-induced cardiac atrophy and body weight loss by signaling through its receptor. Sex differences in cardiac atrophy need to be considered during the treatment of patients suffering from chemotherapy-induced cardiomyopathy to prevent exacerbation of cardiac dysfunction.
大约三分之一的癌症死亡是由恶病质引起的,这是一种严重的骨骼肌和脂肪组织消耗,男性比女性更容易受到影响。癌症患者的心脏也会发生萎缩,但机制和明显的性别差异的基础尚不清楚。在小鼠结肠腺癌模型中,癌症导致心脏质量的丧失,这是由于心肌细胞大小的减少,与所有肌节蛋白水平的降低有关。与骨骼肌恶病质不同,萎缩的心脏不会上调泛素-蛋白酶体系统或其活性,但会增加自噬。因此,癌症导致心脏萎缩的机制与骨骼肌不同。雄性荷瘤小鼠比雌性小鼠表现出更严重的表型,包括更大的心脏质量损失和死亡率、对肿瘤更强的促炎反应以及更大的心脏自噬。在雌性中,雌激素通过其受体信号转导来保护心脏免受癌症引起的萎缩和体重减轻。在治疗因化疗引起的心肌病的患者时,需要考虑心脏萎缩的性别差异,以防止心脏功能恶化。