The Penn State College of Medicine, Department of Cellular and Molecular Physiology, Hershey, PA, USA.
The Penn State College of Medicine, Department of Neural and Behavioral Sciences, Hershey, PA, USA.
Exp Physiol. 2021 Feb;106(2):506-518. doi: 10.1113/EP089130. Epub 2021 Jan 6.
What is the central question of this study? Cachexia causes severe changes in skeletal muscle metabolism and function and is a key predictor of negative outcomes in cancer patients: what are the changes in whole animal energy metabolism and mitochondria in skeletal muscle? What is the main finding and its importance? There is decreased whole animal energy expenditure in mice with cachexia. They displayed highly dysmorphic mitochondria and mitophagy in skeletal muscle.
Cachexia causes changes in skeletal muscle metabolism. Mice with MDA-MB-231 breast cancer bone metastases and cachexia have decreased whole animal energy metabolism and increased skeletal muscle mitophagy. We examined whole animal energy metabolism by indirect calorimetry in mice with MDA-MB-231 breast cancer bone metastases, and showed decreased energy expenditure. We also examined skeletal muscle mitochondria and found that mitochondria in mice with MDA-MB-231 bone metastases are highly dysmorphic and have altered protein markers of mitochondrial biogenesis and dynamics. In addition, LC3B protein was increased in mitochondria of skeletal muscle from cachectic mice, and colocalized with the mitochondrial protein Tom20. Our data demonstrate the importance of mitophagy in cachexia. Understanding these changes will help contribute to defining treatments for cancer cachexia.
本研究的核心问题是什么?恶病质导致骨骼肌代谢和功能发生严重变化,是癌症患者不良预后的关键预测因素:整体动物能量代谢和骨骼肌中线粒体有何变化?主要发现及其重要性是什么?恶病质小鼠的整体动物能量消耗减少。它们的骨骼肌中存在高度畸形的线粒体和线粒体自噬。
恶病质导致骨骼肌代谢发生变化。患有 MDA-MB-231 乳腺癌骨转移和恶病质的小鼠的整体动物能量代谢降低,骨骼肌的线粒体自噬增加。我们通过间接测热法检查了患有 MDA-MB-231 乳腺癌骨转移的小鼠的整体动物能量代谢情况,结果显示能量消耗减少。我们还检查了骨骼肌中的线粒体,发现 MDA-MB-231 骨转移小鼠的线粒体高度畸形,并且线粒体生物发生和动力学的蛋白质标志物发生改变。此外,来自恶病质小鼠骨骼肌的线粒体中 LC3B 蛋白增加,并与线粒体蛋白 Tom20 共定位。我们的数据表明线粒体自噬在恶病质中很重要。了解这些变化将有助于确定癌症恶病质的治疗方法。