NMR Surgical Laboratory, Massachusetts General and Shriners Hospitals, Harvard Medical School, Boston, MA 02114, USA.
Int J Mol Med. 2011 Jan;27(1):15-24. doi: 10.3892/ijmm.2010.557. Epub 2010 Nov 10.
Cancer patients commonly suffer from cachexia, a syndrome in which tumors induce metabolic changes in the host that lead to massive loss in skeletal muscle mass. Using a preclinical mouse model of cancer cachexia, we tested the hypothesis that tumor inoculation causes a reduction in ATP synthesis and genome-wide aberrant expression in skeletal muscle. Mice implanted with Lewis lung carcinomas were examined by in vivo 31P nuclear magnetic resonance (NMR). We examined ATP synthesis rate and the expression of genes that play key-regulatory roles in skeletal muscle metabolism. Our in vivo NMR results showed reduced ATP synthesis rate in tumor-bearing (TB) mice relative to control (C) mice, and were cross-validated with whole genome transcriptome data showing atypical expression levels of skeletal muscle regulatory genes such as peroxisomal proliferator activator receptor γ coactivator 1 ß (PGC-1ß), a major regulator of mitochondrial biogenesis and, mitochondrial uncoupling protein 3 (UCP3). Aberrant pattern of gene expression was also associated with genes involved in inflammation and immune response, protein and lipid catabolism, mitochondrial biogenesis and uncoupling, and inadequate oxidative stress defenses, and these effects led to cachexia. Our findings suggest that reduced ATP synthesis is linked to mitochondrial dysfunction, ultimately leading to skeletal muscle wasting and thus advance our understanding of skeletal muscle dysfunction suffered by cancer patients. This study represents a new line of research that can support the development of novel therapeutics in the molecular medicine of skeletal muscle wasting. Such therapeutics would have wide-spread applications not only for cancer patients, but also for many individuals suffering from other chronic or endstage diseases that exhibit muscle wasting, a condition for which only marginally effective treatments are currently available.
癌症患者通常患有恶病质,这是一种综合征,其中肿瘤诱导宿主发生代谢变化,导致骨骼肌大量丢失。我们使用癌症恶病质的临床前小鼠模型来检验以下假设:肿瘤接种导致 ATP 合成减少和骨骼肌全基因组异常表达。通过体内 31P 核磁共振(NMR)检查植入 Lewis 肺癌的小鼠。我们检查了 ATP 合成率以及在骨骼肌代谢中起关键调节作用的基因的表达。我们的体内 NMR 结果显示,与对照(C)小鼠相比,荷瘤(TB)小鼠的 ATP 合成率降低,这与全基因组转录组数据交叉验证,显示骨骼肌调节基因如过氧化物酶体增殖物激活受体γ共激活因子 1β(PGC-1β)的异常表达水平,这是线粒体生物发生的主要调节剂,和线粒体解偶联蛋白 3(UCP3)。基因表达的异常模式也与参与炎症和免疫反应、蛋白质和脂质分解代谢、线粒体生物发生和解偶联以及氧化应激防御不足的基因相关,这些效应导致恶病质。我们的发现表明,ATP 合成减少与线粒体功能障碍有关,最终导致骨骼肌消耗,从而加深了我们对癌症患者骨骼肌功能障碍的理解。这项研究代表了一条新的研究路线,可以支持骨骼肌消耗的分子医学中新型治疗方法的开发。这些治疗方法不仅将广泛应用于癌症患者,而且还将广泛应用于许多患有其他慢性或终末期疾病的个体,这些疾病都表现出肌肉消耗,而目前只有效果有限的治疗方法。