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Identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics

BACKGROUND: The occurrence of abdominal aortic aneurysms (AAAs) is related to the disorder of immune microenvironment. Cuprotosis was reported to influence the immune microenvironment. The objective of this study is to identify cuprotosis-related genes involved in the pathogenesis and progression of...

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Autores principales: Hu, Jiateng, Xue, Song, Xu, Zhijue, Wu, Zhaoyu, Xu, Xintong, Wang, Xin, Liu, Guang, Lu, Xinwu, Li, Bo, Liu, Xiaobing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150024/
https://www.ncbi.nlm.nih.gov/pubmed/37138870
http://dx.doi.org/10.3389/fimmu.2023.1138126
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author Hu, Jiateng
Xue, Song
Xu, Zhijue
Wu, Zhaoyu
Xu, Xintong
Wang, Xin
Liu, Guang
Lu, Xinwu
Li, Bo
Liu, Xiaobing
author_facet Hu, Jiateng
Xue, Song
Xu, Zhijue
Wu, Zhaoyu
Xu, Xintong
Wang, Xin
Liu, Guang
Lu, Xinwu
Li, Bo
Liu, Xiaobing
author_sort Hu, Jiateng
collection PubMed
description BACKGROUND: The occurrence of abdominal aortic aneurysms (AAAs) is related to the disorder of immune microenvironment. Cuprotosis was reported to influence the immune microenvironment. The objective of this study is to identify cuprotosis-related genes involved in the pathogenesis and progression of AAA. METHODS: Differentially expressed lncRNAs (DElncRNAs) and mRNAs (DEmRNAs) in mouse were identified following AAA through high-throughput RNA sequencing. The enrichment analyses of pathway were selected through Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG). The validation of cuprotosis-related genes was conducted through immunofluorescence and western blot analyses. RESULTS: Totally, 27616 lncRNAs and 2189 mRNAs were observed to be differentially expressed (|Fold Change| ≥ 2 and q< 0.05) after AAA, including 10424 up-regulated and 17192 down-regulated lncRNAs, 1904 up-regulated and 285 down-regulated mRNAs. Gene ontology and KEGG pathway analysis showed that the DElncRNAs and DEmRNAs were implicated in many different biological processes and pathways. Furthermore, Cuprotosis-related genes (NLRP3, FDX1) were upregulated in the AAA samples compared with the normal one. CONCLUSION: Cuprotosis-related genes (NLRP3,FDX1) involved in AAA immune environment might be critical for providing new insight into identification of potential targets for AAA therapy.
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spelling pubmed-101500242023-05-02 Identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics Hu, Jiateng Xue, Song Xu, Zhijue Wu, Zhaoyu Xu, Xintong Wang, Xin Liu, Guang Lu, Xinwu Li, Bo Liu, Xiaobing Front Immunol Immunology BACKGROUND: The occurrence of abdominal aortic aneurysms (AAAs) is related to the disorder of immune microenvironment. Cuprotosis was reported to influence the immune microenvironment. The objective of this study is to identify cuprotosis-related genes involved in the pathogenesis and progression of AAA. METHODS: Differentially expressed lncRNAs (DElncRNAs) and mRNAs (DEmRNAs) in mouse were identified following AAA through high-throughput RNA sequencing. The enrichment analyses of pathway were selected through Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG). The validation of cuprotosis-related genes was conducted through immunofluorescence and western blot analyses. RESULTS: Totally, 27616 lncRNAs and 2189 mRNAs were observed to be differentially expressed (|Fold Change| ≥ 2 and q< 0.05) after AAA, including 10424 up-regulated and 17192 down-regulated lncRNAs, 1904 up-regulated and 285 down-regulated mRNAs. Gene ontology and KEGG pathway analysis showed that the DElncRNAs and DEmRNAs were implicated in many different biological processes and pathways. Furthermore, Cuprotosis-related genes (NLRP3, FDX1) were upregulated in the AAA samples compared with the normal one. CONCLUSION: Cuprotosis-related genes (NLRP3,FDX1) involved in AAA immune environment might be critical for providing new insight into identification of potential targets for AAA therapy. Frontiers Media S.A. 2023-04-17 /pmc/articles/PMC10150024/ /pubmed/37138870 http://dx.doi.org/10.3389/fimmu.2023.1138126 Text en Copyright © 2023 Hu, Xue, Xu, Wu, Xu, Wang, Liu, Lu, Li and Liu 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 Immunology
Hu, Jiateng
Xue, Song
Xu, Zhijue
Wu, Zhaoyu
Xu, Xintong
Wang, Xin
Liu, Guang
Lu, Xinwu
Li, Bo
Liu, Xiaobing
Identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics
title Identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics
title_full Identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics
title_fullStr Identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics
title_full_unstemmed Identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics
title_short Identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics
title_sort identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150024/
https://www.ncbi.nlm.nih.gov/pubmed/37138870
http://dx.doi.org/10.3389/fimmu.2023.1138126
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