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
JOURNAL OF CELL BIOLOGY | 2024年 / 223卷 / 08期
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.
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页数:9
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