Toggle Main Menu Toggle Search

ePrints

Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: Is there a common mechanism?

Lookup NU author(s): Professor Patrick Chinnery, Dr David Samuels, Dr Joanna Elson, Professor Doug Turnbull

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Abstract

In man, cells accumulate somatic mutations of mitochondrial DNA (mtDNA) as part of normal ageing. Although the overall concentration of mutant mtDNA is low in tissue as a whole, very high numbers of various mtDNA mutations develop in individual cells within the same person, which causes age-associated mitochondrial dysfunction. Some tumours contain high numbers of mtDNA mutations that are not present in healthy tissues from the same individual. The proportion of mutant mtDNA also rises in patients with progressive neurological disease due to inherited mtDNA mutations. This increase parallels the relentless clinical progression seen in these disorders. Mathematical models suggest that the same basic cellular mechanisms are responsible for the amplification of mutant mtDNA in ageing, in tumours, and in mtDNA disease. The accumulation of cells that contain high levels of mutant mtDNA may be an inevitable result of the normal mechanisms that maintain cellular concentrations of mtDNA.


Publication metadata

Author(s): Chinnery PF, Samuels DC, Elson J, Turnbull DM

Publication type: Article

Publication status: Published

Journal: Lancet

Year: 2002

Volume: 360

Issue: 9342

Pages: 1323-1325

ISSN (print): 0140-6736

ISSN (electronic): 1474-547X

Publisher: The Lancet Publishing Group

URL: http://dx.doi.org/10.1016/S0140-6736(02)11310-9

DOI: 10.1016/S0140-6736(02)11310-9

PubMed id: 12414225


Altmetrics

Altmetrics provided by Altmetric


Actions

    Link to this publication


Share