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MicroRNAs in ascending thoracic aortic aneurysms
Thoracic Aortic Aneurysm (TAA) is characterized by the dilation of the aorta and is fatal if not diagnosed and treated appropriately. The underlying genetic mechanisms have not been completely delineated, so better knowledge of the physiopathology of TAAs is needed to improve detection and therapy....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385583/ https://www.ncbi.nlm.nih.gov/pubmed/32678444 http://dx.doi.org/10.1042/BSR20200218 |
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author | Moushi, Areti Pillar, Nir Keravnou, Anna Soteriou, Marinos Shomron, Noam Cariolou, Marios A. Bashiardes, Evy |
author_facet | Moushi, Areti Pillar, Nir Keravnou, Anna Soteriou, Marinos Shomron, Noam Cariolou, Marios A. Bashiardes, Evy |
author_sort | Moushi, Areti |
collection | PubMed |
description | Thoracic Aortic Aneurysm (TAA) is characterized by the dilation of the aorta and is fatal if not diagnosed and treated appropriately. The underlying genetic mechanisms have not been completely delineated, so better knowledge of the physiopathology of TAAs is needed to improve detection and therapy. MicroRNAs (miRNAs) regulate gene expression post-transcriptionally and are known to be involved in cardiovascular diseases (CVDs). The current study aimed to identify miRNAs that can be used as possible biomarkers for the early diagnosis of patients with ascending TAAs (ATAAs). MiRNA expression was profiled by NanoString nCounter technology using 12 samples including tissue and pre- and post-surgical plasma from ATAA patients. Four miRNAs were selected and further validated by real time polymerase chain reaction (RT-PCR) in 22 plasma samples from which three miRNAs (hsa-miR140-5p, hsa-miR-191-5p and hsa-miR-214-3p) showed significant expression level differences between the two types of plasma samples. Further analyses of the corresponding predicted target genes by these miRNAs, revealed two genes (Myotubularin-related protein 4 (MTMR4) and Phosphatase 1 catalytic subunit β (PPP1CB)) whose expression was inversely correlated with the expression of their respective miRNAs. Overall, in this pilot study, we identified three miRNAs that might serve as potential biomarkers and therapeutic targets in ATAA. |
format | Online Article Text |
id | pubmed-7385583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73855832020-08-05 MicroRNAs in ascending thoracic aortic aneurysms Moushi, Areti Pillar, Nir Keravnou, Anna Soteriou, Marinos Shomron, Noam Cariolou, Marios A. Bashiardes, Evy Biosci Rep Cardiovascular System & Vascular Biology Thoracic Aortic Aneurysm (TAA) is characterized by the dilation of the aorta and is fatal if not diagnosed and treated appropriately. The underlying genetic mechanisms have not been completely delineated, so better knowledge of the physiopathology of TAAs is needed to improve detection and therapy. MicroRNAs (miRNAs) regulate gene expression post-transcriptionally and are known to be involved in cardiovascular diseases (CVDs). The current study aimed to identify miRNAs that can be used as possible biomarkers for the early diagnosis of patients with ascending TAAs (ATAAs). MiRNA expression was profiled by NanoString nCounter technology using 12 samples including tissue and pre- and post-surgical plasma from ATAA patients. Four miRNAs were selected and further validated by real time polymerase chain reaction (RT-PCR) in 22 plasma samples from which three miRNAs (hsa-miR140-5p, hsa-miR-191-5p and hsa-miR-214-3p) showed significant expression level differences between the two types of plasma samples. Further analyses of the corresponding predicted target genes by these miRNAs, revealed two genes (Myotubularin-related protein 4 (MTMR4) and Phosphatase 1 catalytic subunit β (PPP1CB)) whose expression was inversely correlated with the expression of their respective miRNAs. Overall, in this pilot study, we identified three miRNAs that might serve as potential biomarkers and therapeutic targets in ATAA. Portland Press Ltd. 2020-07-27 /pmc/articles/PMC7385583/ /pubmed/32678444 http://dx.doi.org/10.1042/BSR20200218 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY). |
spellingShingle | Cardiovascular System & Vascular Biology Moushi, Areti Pillar, Nir Keravnou, Anna Soteriou, Marinos Shomron, Noam Cariolou, Marios A. Bashiardes, Evy MicroRNAs in ascending thoracic aortic aneurysms |
title | MicroRNAs in ascending thoracic aortic aneurysms |
title_full | MicroRNAs in ascending thoracic aortic aneurysms |
title_fullStr | MicroRNAs in ascending thoracic aortic aneurysms |
title_full_unstemmed | MicroRNAs in ascending thoracic aortic aneurysms |
title_short | MicroRNAs in ascending thoracic aortic aneurysms |
title_sort | micrornas in ascending thoracic aortic aneurysms |
topic | Cardiovascular System & Vascular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385583/ https://www.ncbi.nlm.nih.gov/pubmed/32678444 http://dx.doi.org/10.1042/BSR20200218 |
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