Ősz Fanni, Nazir Aamir, Takács-Vellai Krisztina, Farkas Zsolt
Department of Biological Anthropology, Eötvös Loránd University, Pázmány P. stny. 1/C, H-1117 Budapest, Hungary.
Laboratory of Functional Genomics and Molecular Toxicology, Division of Toxicology, CSIR-Central Drug Research Institute, Lucknow 226031, India.
Antioxidants (Basel). 2025 Jan 10;14(1):76. doi: 10.3390/antiox14010076.
Mutations in highly conserved genes encoding components of the electron transport chain (ETC) provide valuable insights into the mechanisms of oxidative stress and mitochondrial ROS (mtROS) in a wide range of diseases, including cancer, neurodegenerative disorders, and aging. This review explores the structure and function of the ETC in the context of its role in mtROS generation and regulation, emphasizing its dual roles in cellular damage and signaling. Using as a model organism, we discuss how ETC mutations manifest as developmental abnormalities, lifespan alterations, and changes in mtROS levels. We highlight the utility of redox sensors in for in vivo studies of reactive oxygen species, offering both quantitative and qualitative insights. Finally, we examine the potential of as a platform for testing ETC-targeting drug candidates, including OXPHOS inhibitors, which represent promising avenues in cancer therapeutics. This review underscores the translational relevance of ETC research in , bridging fundamental biology and therapeutic innovation.
编码电子传递链(ETC)组分的高度保守基因中的突变,为深入了解包括癌症、神经退行性疾病和衰老在内的多种疾病中的氧化应激和线粒体活性氧(mtROS)机制提供了有价值的见解。本综述探讨了ETC在mtROS生成和调节中的作用背景下的结构和功能,强调了其在细胞损伤和信号传导中的双重作用。以 作为模式生物,我们讨论了ETC突变如何表现为发育异常、寿命改变和mtROS水平变化。我们强调了氧化还原传感器在 中用于活性氧体内研究的效用,提供了定量和定性的见解。最后,我们研究了 作为测试靶向ETC的候选药物(包括氧化磷酸化抑制剂,这是癌症治疗中有前景的途径)平台的潜力。本综述强调了ETC在 研究中的转化相关性,架起了基础生物学和治疗创新之间的桥梁。