Investigative Treatment Division, Research Center for Innovative Oncology, National Cancer Center Hospital East, Chiba, Japan.
Ann N Y Acad Sci. 2010 Jul;1201:44-9. doi: 10.1111/j.1749-6632.2010.05620.x.
Since deficiencies of critical nutrients and hypoxia are observed in hypovascular tumors, glycolysis alone cannot explain how cancer cells maintain their required energy levels. To study energy metabolism in cancer cells within such tumor microenvironments, we examined the NADH-fumarate reductase system, which is found in anaerobic organisms, such as parasitic helminthes. In human cancer cells cultured under tumor microenvironment-mimicking conditions, mitochondrial NADH-fumarate reductase activity increased in parallel with an increase in fumarate reductase activity, which is the reverse reaction of succinate-ubiquinone reductase and is regulated by the phosphorylation of its subunit. Pyrvinium pamoate, an anthelmintic drug, has an anticancer effect within tumor-mimicking microenvironments. We found that one of the biological mechanisms of pyrvinium is the inhibition of the NADH-fumarate reductase system. Therefore, the NADH-fumarate reductase system might be important for maintaining mitochondrial energy metabolism within the tumor microenvironments and might represent a novel target for anticancer therapies.
由于乏血管肿瘤中存在关键营养物质的缺乏和缺氧,仅糖酵解无法解释癌细胞如何维持其所需的能量水平。为了研究此类肿瘤微环境中的癌细胞内的能量代谢,我们研究了在厌氧生物(如寄生性蠕虫)中发现的烟酰胺腺嘌呤二核苷酸(NADH)-延胡索酸还原酶系统。在模拟肿瘤微环境培养的人癌细胞中,线粒体 NADH-延胡索酸还原酶活性随着延胡索酸还原酶活性的增加而平行增加,而后者是琥珀酸-泛醌还原酶的逆反应,并受其亚基磷酸化的调节。派吡嗪,一种驱虫药,在模拟肿瘤的微环境中具有抗癌作用。我们发现,吡嗪的生物学机制之一是抑制 NADH-延胡索酸还原酶系统。因此,NADH-延胡索酸还原酶系统对于维持肿瘤微环境中的线粒体能量代谢可能很重要,并且可能代表一种新的抗癌治疗靶标。