Cargando…
Persistent DNA damage signaling triggers senescence-associated inflammatory cytokine secretion
Cellular senescence suppresses cancer by stably arresting the proliferation of damaged cells1. Paradoxically, senescent cells also secrete factors that alter tissue microenvironments2. The pathways regulating this secretion are unknown. We show that damaged human cells develop persistent chromatin l...
Autores principales: | Rodier, Francis, Coppé, Jean-Philippe, Patil, Christopher K., Hoeijmakers, Wieteke A. M., Muñoz, Denise P., Raza, Saba R., Freund, Adam, Campeau, Eric, Davalos, Albert R., Campisi, Judith |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743561/ https://www.ncbi.nlm.nih.gov/pubmed/19597488 http://dx.doi.org/10.1038/ncb1909 |
Ejemplares similares
-
Senescent cells as a source of inflammatory factors for tumor progression
por: Davalos, Albert R., et al.
Publicado: (2010) -
Senescence-Associated Secretory Phenotypes Reveal Cell-Nonautonomous Functions of Oncogenic RAS and the p53 Tumor Suppressor
por: Coppé, Jean-Philippe, et al.
Publicado: (2008) -
p53-dependent release of Alarmin HMGB1 is a central mediator of senescent phenotypes
por: Davalos, Albert R., et al.
Publicado: (2013) -
Four faces of cellular senescence
por: Rodier, Francis, et al.
Publicado: (2011) -
A Human-Like Senescence-Associated Secretory Phenotype Is Conserved in Mouse Cells Dependent on Physiological Oxygen
por: Coppé, Jean-Philippe, et al.
Publicado: (2010)