Cellular and molecular mechanisms of stress-induced premature senescence (SIPS) of human diploid fibroblasts and melanocytes.
By O. Toussaint, E. Medrano, T. Zglinicki. Experimental Gerontology, 2000
693 citations recorded by the source corpus.
Subfields: Aging, Dermatology, Physiology
View Paper: https://www.semanticscholar.org/paper/0f0ca4110a479486a336fb0930fb1fa2792199f9
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Citations in the corpus
- Oxidative Stress in Aging Human Skin (2015, background): “Senescence is initiated after such dramatic incidences as severe DNA damage, critical telomere shortening, oxidative stress and hyperactive oncogenic RAS [339–342].”
- Inflammation and aging: signaling pathways and intervention therapies (2023, background): “In the laboratory aging of human diploid fibroblasts (HDFs), as the cells undergo a certain number of population doublings, telomeres become shorter, leading to cell cycle arrest, reduced cell saturation density, and increased cell surface and volume.(280) Hydrogen peroxide is commonly used to induc”
- Ionizing radiation reduces ADAM10 expression in brain microvascular endothelial cells undergoing stress-induced senescence (2017, background): “Premature stress-induced senescence is more common in non-proliferating cells and is caused primarily by oxidative stress and DNA damage [16].”