DNA damage, aging, and cancer

JHJ Hoeijmakers - New England Journal of Medicine, 2009 - Mass Medical Soc
This review gives an account of how the cell repairs DNA damage and presents evidence
that DNA damage contributes to aging and cancer, with the outcome dependent on the type …

Energetics, epigenetics, mitochondrial genetics

DC Wallace, W Fan - Mitochondrion, 2010 - Elsevier
The epigenome has been hypothesized to provide the interface between the environment
and the nuclear DNA (nDNA) genes. Key factors in the environment are the availability of …

Progeria syndromes and ageing: what is the connection?

CR Burtner, BK Kennedy - Nature reviews Molecular cell biology, 2010 - nature.com
One of the many debated topics in ageing research is whether progeroid syndromes are
really accelerated forms of human ageing. The answer requires a better understanding of …

Rapamycin reverses cellular phenotypes and enhances mutant protein clearance in Hutchinson-Gilford progeria syndrome cells

K Cao, JJ Graziotto, CD Blair, JR Mazzulli… - Science translational …, 2011 - science.org
Hutchinson-Gilford progeria syndrome (HGPS) is a lethal genetic disorder characterized by
premature aging. HGPS is most commonly caused by a de novo single-nucleotide …

Human matrix metalloproteinases: an ubiquitarian class of enzymes involved in several pathological processes

D Sbardella, GF Fasciglione, M Gioia, C Ciaccio… - Molecular aspects of …, 2012 - Elsevier
Human matrix metalloproteinases (MMPs) belong to the M10 family of the MA clan of
endopeptidases. They are ubiquitarian enzymes, structurally characterized by an active site …

Histone H4 lysine 16 hypoacetylation is associated with defective DNA repair and premature senescence in Zmpste24-deficient mice

V Krishnan, MZY Chow, Z Wang… - Proceedings of the …, 2011 - National Acad Sciences
Specific point mutations in lamin A gene have been shown to accelerate aging in humans
and mice. Particularly, a de novo mutation at G608G position impairs lamin A processing to …

Resveratrol rescues SIRT1-dependent adult stem cell decline and alleviates progeroid features in laminopathy-based progeria

B Liu, S Ghosh, X Yang, H Zheng, X Liu, Z Wang, G Jin… - Cell metabolism, 2012 - cell.com
Abnormal splicing of LMNA gene or aberrant processing of prelamin A results in progeroid
syndrome. Here we show that lamin A interacts with and activates SIRT1. SIRT1 exhibits …

Structural basis for lamin assembly at the molecular level

J Ahn, I Jo, S Kang, S Hong, S Kim, S Jeong… - Nature …, 2019 - nature.com
Nuclear structure and function are governed by lamins, which are intermediate filaments that
mostly consist of α-helices. Different lamin assembly models have been proposed based on …

Oxidative stress induces an ATM‐independent senescence pathway through p38 MAPK‐mediated lamin B1 accumulation

A Barascu, C Le Chalony, G Pennarun, D Genet… - The EMBO …, 2012 - embopress.org
We report crosstalk between three senescence‐inducing conditions, DNA damage response
(DDR) defects, oxidative stress (OS) and nuclear shape alterations. The recessive …

[HTML][HTML] Aging genetics and aging

S Rodríguez-Rodero, JL Fernández-Morera… - Aging and …, 2011 - ncbi.nlm.nih.gov
The process of aging refers to the decay of an organism's structure and function, in which
molecular and cellular modifications can have various effects at the individual level over the …