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The role of long non-coding RNA in abdominal aortic aneurysm

The abdominal aortic aneurysm (AAA) is characterized by segmental expansion of the abdominal aorta and a high mortality rate. The characteristics of AAA suggest that apoptosis of smooth muscle cells, the production of reactive oxygen species, and inflammation are potential pathways for the formation...

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Detalles Bibliográficos
Autores principales: Xu, Yi, Yang, Shuofei, Xue, Guanhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050724/
https://www.ncbi.nlm.nih.gov/pubmed/37007957
http://dx.doi.org/10.3389/fgene.2023.1153899
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author Xu, Yi
Yang, Shuofei
Xue, Guanhua
author_facet Xu, Yi
Yang, Shuofei
Xue, Guanhua
author_sort Xu, Yi
collection PubMed
description The abdominal aortic aneurysm (AAA) is characterized by segmental expansion of the abdominal aorta and a high mortality rate. The characteristics of AAA suggest that apoptosis of smooth muscle cells, the production of reactive oxygen species, and inflammation are potential pathways for the formation and development of AAA. Long non-coding RNA (lncRNA) is becoming a new and essential regulator of gene expression. Researchers and physicians are focusing on these lncRNAs to use them as clinical biomarkers and new treatment targets for AAAs. LncRNA studies are beginning to emerge, suggesting that they may play a significant but yet unidentified role in vascular physiology and disease. This review examines the role of lncRNA and their target genes in AAA to increase our understanding of the disease’s onset and progression, which is crucial for developing potential AAA therapies.
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spelling pubmed-100507242023-03-30 The role of long non-coding RNA in abdominal aortic aneurysm Xu, Yi Yang, Shuofei Xue, Guanhua Front Genet Genetics The abdominal aortic aneurysm (AAA) is characterized by segmental expansion of the abdominal aorta and a high mortality rate. The characteristics of AAA suggest that apoptosis of smooth muscle cells, the production of reactive oxygen species, and inflammation are potential pathways for the formation and development of AAA. Long non-coding RNA (lncRNA) is becoming a new and essential regulator of gene expression. Researchers and physicians are focusing on these lncRNAs to use them as clinical biomarkers and new treatment targets for AAAs. LncRNA studies are beginning to emerge, suggesting that they may play a significant but yet unidentified role in vascular physiology and disease. This review examines the role of lncRNA and their target genes in AAA to increase our understanding of the disease’s onset and progression, which is crucial for developing potential AAA therapies. Frontiers Media S.A. 2023-03-15 /pmc/articles/PMC10050724/ /pubmed/37007957 http://dx.doi.org/10.3389/fgene.2023.1153899 Text en Copyright © 2023 Xu, Yang and Xue. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Xu, Yi
Yang, Shuofei
Xue, Guanhua
The role of long non-coding RNA in abdominal aortic aneurysm
title The role of long non-coding RNA in abdominal aortic aneurysm
title_full The role of long non-coding RNA in abdominal aortic aneurysm
title_fullStr The role of long non-coding RNA in abdominal aortic aneurysm
title_full_unstemmed The role of long non-coding RNA in abdominal aortic aneurysm
title_short The role of long non-coding RNA in abdominal aortic aneurysm
title_sort role of long non-coding rna in abdominal aortic aneurysm
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050724/
https://www.ncbi.nlm.nih.gov/pubmed/37007957
http://dx.doi.org/10.3389/fgene.2023.1153899
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