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Cellular Senescence: Defining a Path Forward

Gorgoulis, V.; Adams, P. D.; Alimonti, A.; Bennett, D. C.; Bischof, O.; Bishop, C.; Campisi, J.; Collado Rodríguez, Manuel; Evangelou, K.; Ferbeyre, G.; Gil, J.; Hara, E.; Krizhanovsky, V.; Jurk, D.; Maier, A. B.; Narita, M.; Niedernhofer, L.; Passos, J. F.; Robbins, P. D.; Schmitt, C. A.; Sedivy, J.; Vougas, K.; von Zglinicki, T.; Zhou, D. H.; Serrano, M.; Demaria, M.
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URI: http://hdl.handle.net/20.500.11940/15650
PMID: 31675495
DOI: 10.1016/j.cell.2019.10.005
ISSN: 0092-8674
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Cell . 2019 Oct 31;179(4):813-827. doi: 10.1016/j.cell.2019.10.005. (1.286Mb)
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Date issued
2019
Journal title
CELL
Type of content
Artigo
DeCS
cromatina | humanos | puntos de comprobación del ciclo celular | envejecimiento | regulación de la expresión génica
MeSH
Aging | Humans | Gene Expression Regulation | Cell Cycle Checkpoints | Chromatin
Abstract
Cellular senescence is a cell state implicated in various physiological processes and a wide spectrum of age-related diseases. Recently, interest in therapeutically targeting senescence to improve healthy aging and age-related disease, otherwise known as senotherapy, has been growing rapidly. Thus, the accurate detection of senescent cells, especially in vivo, is essential. Here, we present a consensus from the International Cell Senescence Association (ICSA), defining and discussing key cellular and molecular features of senescence and offering recommendations on how to use them as biomarkers. We also present a resource tool to facilitate the identification of genes linked with senescence, SeneQuest (available at http://Senequest.net). Lastly, we propose an algorithm to accurately assess and quantify senescence, both in cultured cells and in vivo.

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