Noncoding RNA control of cellular senescence
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 prot...
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| Published in: | Wiley interdisciplinary reviews. RNA Vol. 6; no. 6; pp. 615 - 629 |
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| Main Authors: | , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Hoboken, USA
John Wiley & Sons, Inc
01.11.2015
Wiley Subscription Services, Inc |
| Subjects: | |
| ISSN: | 1757-7004, 1757-7012 |
| Online Access: | Get full text |
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| Summary: | 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
This article is categorized under:
RNA Interactions with Proteins and Other Molecules > RNA–Protein Complexes
Regulatory RNAs/RNAi/Riboswitches > Regulatory RNAs
RNA in Disease and Development > RNA in Development |
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| Bibliography: | ark:/67375/WNG-3JHRK3F7-G istex:31E4D5072119C3C3771A32B18D95314DF51B4D9B NIA-IRP, NIH ArticleID:WRNA1297 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Feature-3 content type line 23 ObjectType-Review-2 |
| ISSN: | 1757-7004 1757-7012 |
| DOI: | 10.1002/wrna.1297 |