MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, UK.
CRUK Beatson Institute for Cancer Research, Glasgow, UK.
BMC Biol. 2019 Jul 8;17(1):53. doi: 10.1186/s12915-019-0668-y.
Perturbed mitochondrial bioenergetics constitute a core pillar of cancer-associated metabolic dysfunction. While mitochondrial dysfunction in cancer may result from myriad biochemical causes, a historically neglected source is that of the mitochondrial genome. Recent large-scale sequencing efforts and clinical studies have highlighted the prevalence of mutations in mitochondrial DNA (mtDNA) in human tumours and their potential roles in cancer progression. In this review we discuss the biology of the mitochondrial genome, sources of mtDNA mutations, and experimental evidence of a role for mtDNA mutations in cancer. We also propose a 'metabolic licensing' model for mtDNA mutation-derived dysfunction in cancer initiation and progression.
线粒体生物能量学的紊乱是癌症相关代谢功能障碍的核心基础。虽然癌症中线粒体功能障碍可能有多种生化原因,但一个历史上被忽视的来源是线粒体基因组。最近的大规模测序工作和临床研究强调了线粒体 DNA(mtDNA)突变在人类肿瘤中的普遍性及其在癌症进展中的潜在作用。在这篇综述中,我们讨论了线粒体基因组的生物学、mtDNA 突变的来源,以及 mtDNA 突变在癌症中的作用的实验证据。我们还提出了一个“代谢许可”模型,用于解释 mtDNA 突变导致的癌症发生和进展中的功能障碍。