The Medical School, Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.
Biogerontology. 2020 Aug;21(4):445-459. doi: 10.1007/s10522-019-09853-y. Epub 2019 Dec 4.
Alterations in mitochondrial metabolism have been described as one of the major hallmarks of both ageing cells and cancer. Age is the biggest risk factor for the development of a significant number of cancer types and this therefore raises the question of whether there is a link between age-related mitochondrial dysfunction and the advantageous changes in mitochondrial metabolism prevalent in cancer cells. A common underlying feature of both ageing and cancer cells is the presence of somatic mutations of the mitochondrial genome (mtDNA) which we postulate may drive compensatory alterations in mitochondrial metabolism that are advantageous for tumour growth. In this review, we discuss basic mitochondrial functions, mechanisms of mtDNA mutagenesis and their metabolic consequences, and review the evidence for and against a role for mtDNA mutations in cancer development.
线粒体代谢的改变被描述为衰老细胞和癌症的主要特征之一。年龄是许多癌症类型发展的最大风险因素,因此这就提出了一个问题,即与年龄相关的线粒体功能障碍与癌细胞中普遍存在的有利的线粒体代谢变化之间是否存在联系。衰老细胞和癌细胞的一个共同潜在特征是线粒体基因组 (mtDNA) 的体细胞突变,我们推测这些突变可能会驱动线粒体代谢的代偿性改变,有利于肿瘤生长。在这篇综述中,我们讨论了基本的线粒体功能、mtDNA 突变的机制及其代谢后果,并回顾了 mtDNA 突变在癌症发展中的作用的证据。