Noncoding RNA control of cellular senescence

被引:83
作者
Abdelmohsen, Kotb [1 ]
Gorospe, Myriam [1 ]
机构
[1] NIA, Genet Lab, Intramural Res Program, NIH, Baltimore, MD 21224 USA
关键词
REPLICATIVE SENESCENCE; CANCER-CELLS; CYCLE ARREST; STEM-CELLS; CARCINOMA CELLS; GENE-EXPRESSION; GROWTH ARREST; TUMOR-GROWTH; PROLIFERATION; MICRORNA;
D O I
10.1002/wrna.1297
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Senescent cells accumulate in normal tissues with advancing age and arise by long-term culture of primary cells. Senescence develops following exposure to a range of stress-causing agents and broadly influences the physiology and pathology of tissues, organs, and systems in the body. While many proteins are known to control senescence, numerous noncoding (nc)RNAs are also found to promote or repress the senescent phenotype. Here, we review the regulatory ncRNAs (primarily microRNAs and lncRNAs) identified to-date as key modulators of senescence. We highlight the major senescent pathways (p53/p21 and pRB/p16), as well as the senescence-associated secretory phenotype (SASP) and other senescence-associated events governed by ncRNAs, and discuss the importance of understanding comprehensively the ncRNAs implicated in cell senescence. WIREs RNA 2015, 6:615-629. doi: 10.1002/wrna.1297 For further resources related to this article, please visit the .
引用
收藏
页码:615 / 629
页数:15
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