Ikezaki K, Black K L, Conklin S G, Becker D P
Division of Neurosurgery, Jonsson Cancer Center, University of California Los Angeles School of Medicine 90024.
Neurol Res. 1992 Sep;14(4):289-93. doi: 10.1080/01616412.1992.11740072.
The key enzymes of oxidative phosphorylation and glycolysis were evaluated histochemically in rat-implanted C6 gliomas using spot densitometry. Hexokinase, the initial enzyme for the glycolysis pathway, was 40% higher within tumour than the contralateral cerebral cortex. A similar increase within tumours for 2-deoxyglucose was observed by autoradiography. Glucose-6-phosphate dehydrogenase (G6PDH), which is the first enzyme in the pentose phosphate pathway, shunting glucose towards nucleic acid synthesis, was more than 300% higher in gliomas compared with the normal cortex. In contrast, enzymes in the energy producing tricarboxylic acid cycle (succinate-, isocitrate-, and malate-dehydrogenase) and in the electron-transport system (cytochrome c oxidase) were significantly reduced in tumour (58% less than the contralateral cortex). Lactate dehydrogenase activity, which converts pyruvate to lactate, was 50% higher within tumour. Significant reductions of enzymatic activities also occurred in non-neoplastic tissue in ipsilateral hemisphere, with larger tumours. Some enzymes showed heterogeneous activity within tumours, especially G6PDH. These results suggest that: (1) energy production is more dependent on lactate production than on oxidative phosphorylation in C6 glioma, and (2) a significant part of the increased glucose utilization in glioma cells is due to increased activity of the pentose phosphate shunt for increased DNA synthesis, and not energy production.
采用斑点光密度测定法,通过组织化学方法对大鼠植入的C6胶质瘤中氧化磷酸化和糖酵解的关键酶进行了评估。己糖激酶作为糖酵解途径的起始酶,在肿瘤中的含量比同侧大脑皮质高40%。通过放射自显影观察到肿瘤内2-脱氧葡萄糖也有类似的增加。葡萄糖-6-磷酸脱氢酶(G6PDH)是磷酸戊糖途径的首个酶,可使葡萄糖转向核酸合成,与正常皮质相比,其在胶质瘤中的含量高出300%以上。相比之下,参与能量产生的三羧酸循环(琥珀酸脱氢酶、异柠檬酸脱氢酶和苹果酸脱氢酶)以及电子传递系统(细胞色素c氧化酶)中的酶在肿瘤中显著减少(比同侧皮质少58%)。将丙酮酸转化为乳酸的乳酸脱氢酶活性在肿瘤内高出50%。在同侧半球有较大肿瘤的非肿瘤组织中,酶活性也出现显著降低。一些酶在肿瘤内表现出异质性活性,尤其是G6PDH。这些结果表明:(1)在C6胶质瘤中,能量产生更多地依赖于乳酸生成而非氧化磷酸化;(2)胶质瘤细胞中葡萄糖利用增加的很大一部分是由于磷酸戊糖途径活性增加以促进DNA合成,而非能量产生。