TY - JOUR
T1 - Senescent cells
T2 - A novel therapeutic target for aging and age-related diseases
AU - Naylor, R. M.
AU - Baker, D. J.
AU - Van Deursen, J. M.
PY - 2013/1
Y1 - 2013/1
N2 - Aging is the main risk factor for most chronic diseases, disabilities, and declining health. It has been proposed that senescent cells - damaged cells that have lost the ability to divide - drive the deterioration that underlies aging and age-related diseases. However, definitive evidence for this relationship has been lacking. The use of a progeroid mouse model (which expresses low amounts of the mitotic checkpoint protein BubR1) has been instrumental in demonstrating that p16 Ink4a -positive senescent cells drive age-related pathologies and that selective elimination of these cells can prevent or delay age-related deterioration. These studies identify senescent cells as potential therapeutic targets in the treatment of aging and age-related diseases. Here, we describe how senescent cells develop, the experimental evidence that causally implicates senescent cells in age-related dysfunction, the chronic diseases and disorders that are characterized by the accumulation of senescent cells at sites of pathology, and the therapeutic approaches that could specifically target senescent cells.
AB - Aging is the main risk factor for most chronic diseases, disabilities, and declining health. It has been proposed that senescent cells - damaged cells that have lost the ability to divide - drive the deterioration that underlies aging and age-related diseases. However, definitive evidence for this relationship has been lacking. The use of a progeroid mouse model (which expresses low amounts of the mitotic checkpoint protein BubR1) has been instrumental in demonstrating that p16 Ink4a -positive senescent cells drive age-related pathologies and that selective elimination of these cells can prevent or delay age-related deterioration. These studies identify senescent cells as potential therapeutic targets in the treatment of aging and age-related diseases. Here, we describe how senescent cells develop, the experimental evidence that causally implicates senescent cells in age-related dysfunction, the chronic diseases and disorders that are characterized by the accumulation of senescent cells at sites of pathology, and the therapeutic approaches that could specifically target senescent cells.
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U2 - 10.1038/clpt.2012.193
DO - 10.1038/clpt.2012.193
M3 - Article
C2 - 23212104
AN - SCOPUS:84871302192
SN - 0009-9236
VL - 93
SP - 105
EP - 116
JO - Clinical pharmacology and therapeutics
JF - Clinical pharmacology and therapeutics
IS - 1
ER -