Lundholm K, Edström S, Ekman L, Karlberg I, Bylund A C, Scherstén T
Cancer. 1978 Aug;42(2):453-61. doi: 10.1002/1097-0142(197808)42:2<453::aid-cncr2820420212>3.0.co;2-t.
Metabolic alterations in skeletal muscles and liver tissue from cancer patients were compared with corresponding alterations in mice (C-57) with sarcoma (MCG-101). In tumor-bearing man and mice similar changes in enzyme activities and in protein turnover were found. Glycolytic and oxidative enzyme activities were decreased in skeletal muscle tissue. Tumor-associated increase in lysosomal enzyme activities was found in both species. Leucine was incorporated into skeletal muscle proteins at a lower rate and into hepatic proteins at a higher rate in both species with malignant tumor. In tumor-bearing mice ribosome profiles from skeletal muscle, heart muscle and liver showed a preponderance of slowly sedimenting units of polyribosomes suggesting that initiation of protein synthesis may be a rate limiting step. The metabolic host reactions in tumor-bearing mice were similar to those in cancer patients implying that experimental tumors are relevant to use for analysis of mechanisms behind the development of cancer cachexia in man.
将癌症患者骨骼肌和肝脏组织中的代谢改变与患有肉瘤(MCG - 101)的小鼠(C - 57)的相应改变进行了比较。在患肿瘤的人和小鼠中,发现酶活性和蛋白质周转有相似的变化。骨骼肌组织中的糖酵解和氧化酶活性降低。在这两个物种中均发现与肿瘤相关的溶酶体酶活性增加。在患有恶性肿瘤的两个物种中,亮氨酸掺入骨骼肌蛋白的速率较低,而掺入肝脏蛋白的速率较高。在患肿瘤的小鼠中,骨骼肌、心肌和肝脏的核糖体图谱显示多核糖体缓慢沉降单位占优势,这表明蛋白质合成的起始可能是一个限速步骤。患肿瘤小鼠的代谢宿主反应与癌症患者相似,这意味着实验性肿瘤可用于分析人类癌症恶病质发生背后的机制。