共 50 条
Regulation of cell function and identity by cellular senescence
被引:2
|作者:
Huna, Anda
[1
]
Massemin, Amelie
[1
]
Makulyte, Gabriela
[1
]
Flaman, Jean-Michel
[1
]
Martin, Nadine
[1
]
Bernard, David
[1
]
机构:
[1] Univ Lyon, CNRS UMR 5286, Equipe Labellisee Ligue Contre Canc, Inserm U1052,Ctr Rech Cancerol Lyon,Ctr Leon Berar, Lyon, France
来源:
关键词:
ONCOGENE-INDUCED SENESCENCE;
LIVER-CANCER;
TELOMERASE;
CULTURE;
GROWTH;
TUMORIGENESIS;
SURVEILLANCE;
MECHANISMS;
SECRETION;
BARRIER;
D O I:
10.1083/jcb.202401112
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Huna et al. provide insights into the shifting perception of cellular senescence: from a mere cell proliferation arrest to a reinforcement or change of cell identity. During aging and in some contexts, like embryonic development, wound healing, and diseases such as cancer, senescent cells accumulate and play a key role in different pathophysiological functions. A long-held belief was that cellular senescence decreased normal cell functions, given the loss of proliferation of senescent cells. This view radically changed following the discovery of the senescence-associated secretory phenotype (SASP), factors released by senescent cells into their microenvironment. There is now accumulating evidence that cellular senescence also promotes gain-of-function effects by establishing, reinforcing, or changing cell identity, which can have a beneficial or deleterious impact on pathophysiology. These effects may involve both proliferation arrest and autocrine SASP production, although they largely remain to be defined. Here, we provide a historical overview of the first studies on senescence and an insight into emerging trends regarding the effects of senescence on cell identity.
引用
收藏
页数:9
相关论文