Cargando…

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....

Descripción completa

Detalles Bibliográficos
Autores principales: Moushi, Areti, Pillar, Nir, Keravnou, Anna, Soteriou, Marinos, Shomron, Noam, Cariolou, Marios A., Bashiardes, Evy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
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
_version_ 1783563815226441728
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
work_keys_str_mv AT moushiareti micrornasinascendingthoracicaorticaneurysms
AT pillarnir micrornasinascendingthoracicaorticaneurysms
AT keravnouanna micrornasinascendingthoracicaorticaneurysms
AT soterioumarinos micrornasinascendingthoracicaorticaneurysms
AT shomronnoam micrornasinascendingthoracicaorticaneurysms
AT carioloumariosa micrornasinascendingthoracicaorticaneurysms
AT bashiardesevy micrornasinascendingthoracicaorticaneurysms