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dc.contributor.authorEfovi, D
dc.contributor.authorXiao, Q
dc.date.accessioned2024-01-30T09:05:45Z
dc.date.available2022-12-20
dc.date.available2024-01-30T09:05:45Z
dc.date.issued2022-12-22
dc.identifier.otherARTN 24
dc.identifier.otherARTN 24
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/94307
dc.description.abstractIn-stent restenosis (ISR), characterised by ≥50% re-narrowing of the target vessel, is a common complication following stent implantation and remains a significant challenge to the long-term success of angioplasty procedures. Considering the global burden of cardiovascular diseases, improving angioplasty patient outcomes remains a key priority. Noncoding RNAs (ncRNAs) including microRNA (miRNA), long noncoding RNA (lncRNA) and circular RNA (circRNA) have been extensively implicated in vascular cell biology and ISR through multiple, both distinct and overlapping, mechanisms. Vascular smooth muscle cells, endothelial cells and macrophages constitute the main cell types involved in the multifactorial pathophysiology of ISR. The identification of critical regulators exemplified by ncRNAs in all these cell types and processes makes them an exciting therapeutic target in the field of restenosis. In this review, we will comprehensively explore the potential functions and underlying molecular mechanisms of ncRNAs in vascular cell biology in the context of restenosis, with an in-depth focus on vascular cell dysfunction during restenosis development and progression. We will also discuss the diagnostic biomarker and therapeutic target potential of ncRNAs in ISR. Finally, we will discuss the current shortcomings, challenges, and perspectives toward the clinical application of ncRNAs.en_US
dc.publisherMDPIen_US
dc.relation.ispartofBIOLOGY-BASEL
dc.rightsThis article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/4.0/).
dc.subjectnoncoding RNAsen_US
dc.subjectmicroRNAsen_US
dc.subjectlong noncoding RNAsen_US
dc.subjectcircRNAsen_US
dc.subjectvascular cellsen_US
dc.subjectsmooth muscle cellsen_US
dc.subjectendothelial cellsen_US
dc.subjectrestenosisen_US
dc.subjectin-stent restenosisen_US
dc.subjectneointimal hyperplasiaen_US
dc.subjectcardiovascular diseaseen_US
dc.titleNoncoding RNAs in Vascular Cell Biology and Restenosisen_US
dc.typeArticleen_US
dc.rights.holder© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
dc.identifier.doi10.3390/biology12010024
pubs.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000914230900001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume12en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
qmul.funderFunctional roles of hnRNPA1 in vascular smooth muscle cell phenotype modulation and neointima hyperplasia::British Heart Foundationen_US
qmul.funderFunctional roles of hnRNPA1 in vascular smooth muscle cell phenotype modulation and neointima hyperplasia::British Heart Foundationen_US
qmul.funderFunctional roles of hnRNPA1 in vascular smooth muscle cell phenotype modulation and neointima hyperplasia::British Heart Foundationen_US
qmul.funderFunctional roles of hnRNPA1 in vascular smooth muscle cell phenotype modulation and neointima hyperplasia::British Heart Foundationen_US


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