Aberrant mitochondrial function in ageing and cancer

被引:18
作者
Whitehall, Julia C. [1 ]
Greaves, Laura C. [1 ]
机构
[1] Newcastle Univ, Sch Med, Wellcome Ctr Mitochondrial Res, Inst Neurosci, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Mitochondria; Ageing; Cancer; Metabolism; mtDNA mutations; OXIDATIVE DNA-DAMAGE; SUPEROXIDE-DISMUTASE; S-ADENOSYLMETHIONINE; SIGNAL-TRANSDUCTION; ELECTRON-TRANSPORT; RESPIRATORY-CHAIN; POINT MUTATIONS; METABOLISM; MTDNA; APOPTOSIS;
D O I
10.1007/s10522-019-09853-y
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
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.
引用
收藏
页码:445 / 459
页数:15
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