Department of Cell Biology and Infection, Membrane Traffic and Pathogenesis Unit, Pasteur Institute, 25, rue du Dr. Roux, 75724 Paris Cedex 15, France.
Chembiochem. 2012 May 29;13(8):1191-8. doi: 10.1002/cbic.201200065. Epub 2012 Apr 24.
The natural product gambogic acid (GA) has shown significant potential as an anticancer agent as it is able to induce apoptosis in multiple tumor cell lines, including multidrug-resistant cell lines, as well as displaying antitumor activity in animal models. Despite the fact that GA has entered phase I clinical trials, the primary cellular target and mode of action of this compound remain unclear, although many proteins have been shown to be affected by it. By thorough analysis of several cellular organelles, at both the morphological and functional levels, we demonstrate that the primary effect of GA is at the mitochondria. We found that GA induces mitochondrial damage within minutes of incubation at low-micromolar concentrations. Moreover, a fluorescent derivative of GA was able to localize specifically to the mitochondria and was displaced from these organelles after competition with unlabeled GA. These findings indicate that GA directly targets the mitochondria to induce the intrinsic pathway of apoptosis, and thus represents a new member of the mitocans.
天然产物藤黄酸(GA)已显示出作为抗癌剂的巨大潜力,因为它能够诱导多种肿瘤细胞系凋亡,包括多药耐药细胞系,并且在动物模型中显示出抗肿瘤活性。尽管 GA 已进入 I 期临床试验,但该化合物的主要细胞靶标和作用方式仍不清楚,尽管已经证明许多蛋白质受到它的影响。通过对几种细胞细胞器进行彻底的分析,在形态和功能水平上,我们证明 GA 的主要作用是在线粒体上。我们发现,GA 在低微摩尔浓度孵育数分钟内即可诱导线粒体损伤。此外,GA 的荧光衍生物能够特异性地定位于线粒体,并在与未标记的 GA 竞争后从这些细胞器中移位。这些发现表明 GA 直接靶向线粒体以诱导细胞凋亡的内在途径,因此代表了新型的线粒体靶向药物。