SASP regulation by noncoding RNA

被引:67
作者
Panda, Amaresh C. [1 ]
Abdelmohsen, Kotb [1 ]
Gorospe, Myriam [1 ]
机构
[1] NIA, Lab Genet & Genom, Intramural Res Program, NIH, Baltimore, MD 21224 USA
关键词
Transcriptome; Post-transcriptional gene regulation; Noncoding RNA; Long noncoding RNA; microRNA; mRNA stability; mRNA translation; Ribonucleoprotein complexes; Transcriptional gene regulation; Aging; Inflammatory cytokines; Senescence; CELLULAR SENESCENCE; SECRETORY PHENOTYPE; CIRCULAR RNAS; MICRORNA BIOGENESIS; GENE-EXPRESSION; DOWN-REGULATION; TNF-ALPHA; CANCER; CELLS; AGE;
D O I
10.1016/j.mad.2017.05.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Noncoding RNAs (ncRNAs), including micro (mi)RNAs, long noncoding (lnc)RNAs, and circular (circ)RNAs, control specific gene expression programs by regulating transcriptional, post-transcriptional, and post-translational processes. Through their broad influence on protein expression and function, ncRNAs have been implicated in virtually all cellular processes such as proliferation, senescence, quiescence, differentiation, apoptosis, and the stress and immune responses. Senescence is a cellular phenotype associated with the physiologic decline of aging and with age-related pathologies. Besides their characteristic terminal growth arrest and differential gene expression programs, senescent cells are known to secrete potent pro-inflammatory, angiogenic, and tissue-remodeling factors. This important trait, known as the senescence-associated secretory phenotype (SASP), influences many biological processes such as tissue repair and regeneration, tumorigenesis, and the aging-associated pro-inflammatory state. Here, we review the microRNAs, lncRNAs, and circRNAs that influence the production of SASP factors and discuss the rising interest in SASP-regulatory ncRNAs as diagnostic and therapeutic targets.
引用
收藏
页码:37 / 43
页数:7
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