“…Thus far, replication-competent cell types that undergo senescence include fibroblasts, epithelial cells, melanocytes, endothelial cells, astrocytes and many others (Bitto et al, 2010; Coppe et al, 2010; Coppe et al, 2008; Voghel et al, 2007; Wajapeyee et al, 2008). The senescence response arrests cell proliferation, stably and essentially irreversibly, in response to stresses that puts cells at risk for malignant transformation (Campisi, 2001; Collado and Serrano, 2010; Prieri et al, 2008). These stresses include repeated cell division that erodes telomeres (perceived by cells as severely damaged DNA), DNA damage anywhere in the genome, and disrupted chromatin (epigenomic damage) (Campisi, 2007; Guney et al, 2006; Rodier et al, 2005; Shay and Wright, 2005).…”