衰老
生物
细胞生物学
有丝分裂
癌变
细胞周期
细胞凋亡
细胞衰老
癌症研究
表型
细胞
细胞生长
细胞周期检查点
程序性细胞死亡
遗传学
癌症
基因
作者
Przemysław Sapieha,Frédérick A. Mallette
标识
DOI:10.1016/j.tcb.2018.03.003
摘要
In mitotic cells, cellular senescence is a permanent state of G1 arrest, that may have evolved in parallel to apoptosis, to limit proliferation of damaged cells and oncogenesis. Recent studies have suggested that postmitotic cells are also capable of entering a state of senescence, although the repercussions of postmitotic cellular senescence (PoMiCS) on tissue health and function are currently ill-defined. In tissues made largely of post-mitotic cells, it is evolutionary advantageous to preserve cellular integrity and cellular senescence of post-mitotic cells may prevent stressor-induced tissue degeneration and promote tissue repair. Paradoxically, PoMiCS may also contribute to disease progression through the generation of inflammatory mediators, termed the senescence-associated secretory phenotype. Here, we discuss the potential roles of PoMiCS and propose to enlarge the current definition of cellular senescence to postmitotic terminally differentiated cells.
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