Cargando…

Ubiquitin-specific protease as the underlying gene biomarker for aortic stenosis

BACKGROUND: Aortic stenosis is a common heart valvular disease whose pathological processes include an inflammatory reaction and lipid accumulation. However, its detailed pathogenesis is yet to be completely elucidated. Therefore, it is of great significance to further explore the molecular mechanis...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Yin, Wang, Lian-qun, Yao, Bo-chen, Guo, Zhi-gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260852/
https://www.ncbi.nlm.nih.gov/pubmed/32471496
http://dx.doi.org/10.1186/s12944-020-01299-3
_version_ 1783540407166042112
author Yang, Yin
Wang, Lian-qun
Yao, Bo-chen
Guo, Zhi-gang
author_facet Yang, Yin
Wang, Lian-qun
Yao, Bo-chen
Guo, Zhi-gang
author_sort Yang, Yin
collection PubMed
description BACKGROUND: Aortic stenosis is a common heart valvular disease whose pathological processes include an inflammatory reaction and lipid accumulation. However, its detailed pathogenesis is yet to be completely elucidated. Therefore, it is of great significance to further explore the molecular mechanisms of aortic stenosis. METHODS: Four datasets were downloaded from the Gene Expression Omnibus (GEO) database. Firstly, the differently expressed genes (DEGs) were screened between control and aortic stenosis samples. Secondly, weighted gene co-expression network analysis (WGCNA) was performed to find the highly relevant gene modules. Enrichment analysis and protein-protein interaction (PPI) networking were also performed, then Cytoscape was used to identify hub genes. Finally, the six participants (3 control participants and 3 patients with aortic stenosis) were recruited at the Tianjin Chest Hospital. In order to verify the expression level of USP14, several molecular experiments were performed, including hematoxylin-eosin (HE) staining, immunohistochemistry, immunofluorescence technology, real time-quantitative polymerase chain reaction (RT-qPCR), and western blotting. RESULTS: A total of 9636 DEGs were found between the control and aortic stenosis samples. The DEGs were mainly enriched in the autophagy-animal, cellular lipid catabolic process, apoptosis, and glycoside metabolic process categories. Eleven hub genes were identified via four different algorithms. Following verification of the patient samples, Ubiquitin-specific protease 14 (USP14) was found to be displayed at higher levels in the aortic stenosis samples. CONCLUSION: USP14 might be involved in the occurrence and development of aortic stenosis, so it would be a molecular target for early diagnosis and specific treatment of aortic stenosis. There is a significant association between the high expression of USP14 and aortic stenosis, indicating that this gene may be a genetic risk factor for aortic stenosis.
format Online
Article
Text
id pubmed-7260852
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-72608522020-06-07 Ubiquitin-specific protease as the underlying gene biomarker for aortic stenosis Yang, Yin Wang, Lian-qun Yao, Bo-chen Guo, Zhi-gang Lipids Health Dis Research BACKGROUND: Aortic stenosis is a common heart valvular disease whose pathological processes include an inflammatory reaction and lipid accumulation. However, its detailed pathogenesis is yet to be completely elucidated. Therefore, it is of great significance to further explore the molecular mechanisms of aortic stenosis. METHODS: Four datasets were downloaded from the Gene Expression Omnibus (GEO) database. Firstly, the differently expressed genes (DEGs) were screened between control and aortic stenosis samples. Secondly, weighted gene co-expression network analysis (WGCNA) was performed to find the highly relevant gene modules. Enrichment analysis and protein-protein interaction (PPI) networking were also performed, then Cytoscape was used to identify hub genes. Finally, the six participants (3 control participants and 3 patients with aortic stenosis) were recruited at the Tianjin Chest Hospital. In order to verify the expression level of USP14, several molecular experiments were performed, including hematoxylin-eosin (HE) staining, immunohistochemistry, immunofluorescence technology, real time-quantitative polymerase chain reaction (RT-qPCR), and western blotting. RESULTS: A total of 9636 DEGs were found between the control and aortic stenosis samples. The DEGs were mainly enriched in the autophagy-animal, cellular lipid catabolic process, apoptosis, and glycoside metabolic process categories. Eleven hub genes were identified via four different algorithms. Following verification of the patient samples, Ubiquitin-specific protease 14 (USP14) was found to be displayed at higher levels in the aortic stenosis samples. CONCLUSION: USP14 might be involved in the occurrence and development of aortic stenosis, so it would be a molecular target for early diagnosis and specific treatment of aortic stenosis. There is a significant association between the high expression of USP14 and aortic stenosis, indicating that this gene may be a genetic risk factor for aortic stenosis. BioMed Central 2020-05-29 /pmc/articles/PMC7260852/ /pubmed/32471496 http://dx.doi.org/10.1186/s12944-020-01299-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yang, Yin
Wang, Lian-qun
Yao, Bo-chen
Guo, Zhi-gang
Ubiquitin-specific protease as the underlying gene biomarker for aortic stenosis
title Ubiquitin-specific protease as the underlying gene biomarker for aortic stenosis
title_full Ubiquitin-specific protease as the underlying gene biomarker for aortic stenosis
title_fullStr Ubiquitin-specific protease as the underlying gene biomarker for aortic stenosis
title_full_unstemmed Ubiquitin-specific protease as the underlying gene biomarker for aortic stenosis
title_short Ubiquitin-specific protease as the underlying gene biomarker for aortic stenosis
title_sort ubiquitin-specific protease as the underlying gene biomarker for aortic stenosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260852/
https://www.ncbi.nlm.nih.gov/pubmed/32471496
http://dx.doi.org/10.1186/s12944-020-01299-3
work_keys_str_mv AT yangyin ubiquitinspecificproteaseastheunderlyinggenebiomarkerforaorticstenosis
AT wanglianqun ubiquitinspecificproteaseastheunderlyinggenebiomarkerforaorticstenosis
AT yaobochen ubiquitinspecificproteaseastheunderlyinggenebiomarkerforaorticstenosis
AT guozhigang ubiquitinspecificproteaseastheunderlyinggenebiomarkerforaorticstenosis