Hwang Ming-Shih, Rohlena Jakub, Dong Lan-Feng, Neuzil Jiri, Grimm Stefan
Division of Experimental Medicine, Imperial College London, Hammersmith Campus, Du Cane Road, London W12 0NN, UK.
Institute of Biotechnology, Academy of Sciences of the Czech Republic, Prague 142 20, Czech Republic.
Mitochondrion. 2014 Nov;19 Pt A:20-8. doi: 10.1016/j.mito.2014.06.001. Epub 2014 Jun 13.
Complex II of the respiratory chain (RC) recently emerged as a prominent regulator of cell death. In both cancer cells as well as neurodegenerative diseases, mutations in subunits have been found along with other genetic alterations indirectly affecting this complex. Anticancer compounds were developed that target complex II and cause cell death in a tumor-specific way. Our mechanistic understanding of how complex II is activated for cell death induction has recently been made clearer in recent studies, the results of which are covered in this review. This protein assembly is specifically activated for cell death via the dissociation of its SDHA and SDHB subunits from the membrane-anchoring proteins through pH change or mitochondrial Ca(2+) influx. The SDH activity contained in the SDHA/SDHB subcomplex remains intact and then generates, in an uncontrolled fashion, excessive amounts of reactive oxygen species (ROS) for cell death. Future studies on this mitochondrial complex will further elucidate it as a target for cancer treatments and reveal its role as a nexus for many diverse stimuli in cell death signaling.
呼吸链(RC)的复合物II最近成为细胞死亡的重要调节因子。在癌细胞和神经退行性疾病中,均发现了亚基突变以及其他间接影响该复合物的基因改变。已开发出靶向复合物II并以肿瘤特异性方式导致细胞死亡的抗癌化合物。最近的研究使我们对复合物II如何被激活以诱导细胞死亡的机制有了更清晰的认识,本综述涵盖了这些研究结果。这种蛋白质组装体通过其SDHA和SDHB亚基通过pH变化或线粒体Ca(2+)内流从膜锚定蛋白解离而被特异性激活以诱导细胞死亡。SDHA/SDHB亚复合物中所含的SDH活性保持完整,然后以不受控制的方式产生过量的活性氧(ROS)以导致细胞死亡。对这种线粒体复合物的未来研究将进一步阐明其作为癌症治疗靶点的作用,并揭示其作为细胞死亡信号传导中多种不同刺激的连接点的作用。