共 50 条
Epigenetic regulation in cell senescence
被引:44
|作者:
Cheng, Li-Qin
[1
,2
]
Zhang, Zhu-Qin
[1
,2
]
Chen, Hou-Zao
[1
,2
]
Liu, De-Pei
[1
,2
]
机构:
[1] Chinese Acad Med Sci, Inst Basic Med Sci, Dept Biochem & Mol Biol, State Key Lab Med Mol Biol, Beijing 100005, Peoples R China
[2] Peking Union Med Coll, Beijing 100005, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Senescence;
DNA methylation;
Histone modification;
Chromatin remodelling complex;
ncRNA;
CHROMATIN REMODELING COMPLEX;
TELOMERASE REVERSE-TRANSCRIPTASE;
MESENCHYMAL STROMAL CELLS;
DNA-DAMAGE RESPONSE;
REPLICATIVE SENESCENCE;
HISTONE MODIFICATIONS;
ENDOTHELIAL-CELLS;
DOWN-REGULATION;
CANCER-CELLS;
SECRETORY PHENOTYPE;
D O I:
10.1007/s00109-017-1581-x
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Cell senescence, which is an irreversible state of cell proliferative arrest, has emerged as a potentially important contributor to tissue dysfunction and organismal ageing. Cell senescence is triggered by a variety of senescence stressors, which affect gene expression and multiple signalling pathways that give rise to various senescence phenotypes. Epigenetic mechanisms, as critical regulators of chromosomal architecture and gene expression, have added an extra dimension to the molecular mechanisms of cell senescence. Cell senescence is accompanied by changes in DNA methylation, histone-associated epigenetic processes, chromatin remodelling and ncRNA expression. Those senescence-associated epigenetic alterations interact with the senescence regulatory programme networks and lead to various cell senescence phenotypes. This review provides a comprehensive overview of epigenetic changes and their effects on cell senescence. The differences in epigenetic alterations among different types of senescence are also discussed. Furthermore, we summarise the interactions among different epigenetic mechanisms during cell senescence and analyse the possibility of using epigenetic signatures as biomarkers and therapeutic targets for the treatment of senescence-associated diseases.
引用
收藏
页码:1257 / 1268
页数:12
相关论文