“…Given that random mutations result in the formation of predominantly deleterious allele [ 1 , 46 , 47 , 86 , 87 ], their accumulation in cells during aging will translate into a decrease in functional proficiency, including proliferative and regenerative capacity [ 88 , 89 ]. For example, liver regeneration is delayed in elderly patients [ 90 ] and experimental animals [ 88 ], and this is due, at least in part, to a cell-autonomous decrease in proliferative potential of the aged hepatocyte [ 91 ]. Moreover, it adds to the observation referred to above that the aged liver microenvironment is clonogenic to both normal [ 62 ] and pre-neoplastic [ 63 ] transplanted hepatocytes.…”