Cruz-Bermúdez A, Vicente-Blanco R J, Gonzalez-Vioque E, Provencio M, Fernández-Moreno M Á, Garesse R
Departamento de Bioquímica and Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), Facultad de Medicina, UAM, Madrid, Spain.
Instituto de Investigaciones Biomédicas "Alberto Sols", Consejo Superior de Investigaciones Científicas (CSIC), Universidad Autónoma de Madrid (UAM), C/Arturo Duperier 4, Madrid, Spain.
Clin Transl Oncol. 2017 Apr;19(4):409-418. doi: 10.1007/s12094-016-1561-6. Epub 2016 Oct 24.
The potential role of the mitochondrial genome has recently attracted interest because of its high mutation frequency in tumors. Different aspects of mtDNA make it relevant for cancer's biology, such as it encodes a limited but essential number of genes for OXPHOS biogenesis, it is particularly susceptible to mutations, and its copy number can vary. Moreover, most ROS in mitochondria are produced by the electron transport chain. These characteristics place the mtDNA in the center of multiple signaling pathways, known as mitochondrial retrograde signaling, which modifies numerous key processes in cancer. Cybrid studies support that mtDNA mutations are relevant and exert their effect through a modification of OXPHOS function and ROS production. However, there is still much controversy regarding the clinical relevance of mtDNA mutations. New studies should focus more on OXPHOS dysfunction associated with a specific mutational signature rather than the presence of mutations in the mtDNA.
线粒体基因组的潜在作用最近因其在肿瘤中的高突变频率而受到关注。线粒体DNA的不同方面使其与癌症生物学相关,例如它编码数量有限但对氧化磷酸化生物合成至关重要的基因,它特别容易发生突变,并且其拷贝数会发生变化。此外,线粒体中的大多数活性氧是由电子传递链产生的。这些特征使线粒体DNA处于多个信号通路的中心,即所谓的线粒体逆行信号通路,该通路会改变癌症中的许多关键过程。细胞杂交研究支持线粒体DNA突变是相关的,并通过改变氧化磷酸化功能和活性氧产生来发挥作用。然而,关于线粒体DNA突变的临床相关性仍存在很多争议。新的研究应更多地关注与特定突变特征相关的氧化磷酸化功能障碍,而不是线粒体DNA中突变的存在。