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Cellular senescence and the senescent secretory phenotype: therapeutic opportunities

Tamar Tchkonia, Yi Zhu, Jan van Deursen, Judith Campisi, James L. Kirkland

Journal of Clinical Investigation · 2013 · ▲ 1,748 citations

Abstract

Aging is the largest risk factor for most chronic diseases, which account for the majority of morbidity and health care expenditures in developed nations. New findings suggest that aging is a modifiable risk factor, and it may be feasible to delay age-related diseases as a group by modulating fundamental aging mechanisms. One such mechanism is cellular senescence(definition), which can cause chronic inflammation through the senescence-associated secretory phenotype (SASP). We review the mechanisms that induce senescence and the SASP, their associations with chronic disease and frailty, therapeutic opportunities based on targeting senescent cells and the SASP, and potential paths to developing clinical interventions.

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Provenance

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OpenAlex
DOI
10.1172/jci64098
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2026-05-31 MST

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APA
Tchkonia, T., Zhu, Y., Deursen, J.V., Campisi, J., &amp; Kirkland, J.L. (2013). Cellular senescence and the senescent secretory phenotype: therapeutic opportunities. <em>Journal of Clinical Investigation</em>. https://doi.org/10.1172/jci64098
Vancouver
Tchkonia T, Zhu Y, Deursen JV, Campisi J, Kirkland JL. Cellular senescence and the senescent secretory phenotype: therapeutic opportunities. Journal of Clinical Investigation. 2013. doi:10.1172/jci64098.
BibTeX
@article{tamar2013Cellul, title = {Cellular senescence and the senescent secretory phenotype: therapeutic opportunities}, author = {Tamar Tchkonia and Yi Zhu and Jan van Deursen and Judith Campisi and James L. Kirkland}, journal = {Journal of Clinical Investigation}, year = {2013}, doi = {10.1172/jci64098}, }

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