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Identification of Novel Plasma Biomarkers for Abdominal Aortic Aneurysm by Protein Array Analysis
Abdominal aortic aneurysm (AAA) is a potentially life-threatening disease that is common in the aging population. Currently, there are no approved diagnostic biomarkers or therapeutic drugs for AAA. We aimed to identify novel plasma biomarkers or potential therapeutic targets for AAA using a high-th...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775419/ https://www.ncbi.nlm.nih.gov/pubmed/36551281 http://dx.doi.org/10.3390/biom12121853 |
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author | Wu, Jianqiang Wang, Wei Xie, Ting Chen, Zhaoran Zhou, Lei Song, Xiaohong Kan, Haoxuan Lv, Yanze Wu, Lianglin Li, Fangda Yang, Dan Chen, Yuexin Liu, Bao Zheng, Yuehong |
author_facet | Wu, Jianqiang Wang, Wei Xie, Ting Chen, Zhaoran Zhou, Lei Song, Xiaohong Kan, Haoxuan Lv, Yanze Wu, Lianglin Li, Fangda Yang, Dan Chen, Yuexin Liu, Bao Zheng, Yuehong |
author_sort | Wu, Jianqiang |
collection | PubMed |
description | Abdominal aortic aneurysm (AAA) is a potentially life-threatening disease that is common in the aging population. Currently, there are no approved diagnostic biomarkers or therapeutic drugs for AAA. We aimed to identify novel plasma biomarkers or potential therapeutic targets for AAA using a high-throughput protein array-based method. Proteomics expression profiles were investigated in plasma from AAA patients and healthy controls (HC) using 440-cytokine protein array analysis. Several promising biomarkers were further validated in independent cohorts using enzyme-linked immunosorbent assay (ELISA). Thirty-nine differentially expressed plasma proteins were identified between AAA and HC. Legumain (LGMN) was significantly higher in AAA patients and was validated in another large cohort. Additionally, “AAA without diabetes” (AAN) patients and “AAA complicated with type 2 diabetes mellitus” (AAM) patients had different cytokine expression patterns in their plasma, and nine plasma proteins were differentially expressed among the AAN, AAM, and HC subjects. Delta-like protein 1 (DLL1), receptor tyrosine-protein kinase erbB-3 (ERBB3), and dipeptidyl peptidase 4 (DPPIV) were significantly higher in AAM than in AAN. This study identified several promising plasma biomarkers of AAA. Their role as therapeutic targets for AAA warrants further investigation. |
format | Online Article Text |
id | pubmed-9775419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97754192022-12-23 Identification of Novel Plasma Biomarkers for Abdominal Aortic Aneurysm by Protein Array Analysis Wu, Jianqiang Wang, Wei Xie, Ting Chen, Zhaoran Zhou, Lei Song, Xiaohong Kan, Haoxuan Lv, Yanze Wu, Lianglin Li, Fangda Yang, Dan Chen, Yuexin Liu, Bao Zheng, Yuehong Biomolecules Article Abdominal aortic aneurysm (AAA) is a potentially life-threatening disease that is common in the aging population. Currently, there are no approved diagnostic biomarkers or therapeutic drugs for AAA. We aimed to identify novel plasma biomarkers or potential therapeutic targets for AAA using a high-throughput protein array-based method. Proteomics expression profiles were investigated in plasma from AAA patients and healthy controls (HC) using 440-cytokine protein array analysis. Several promising biomarkers were further validated in independent cohorts using enzyme-linked immunosorbent assay (ELISA). Thirty-nine differentially expressed plasma proteins were identified between AAA and HC. Legumain (LGMN) was significantly higher in AAA patients and was validated in another large cohort. Additionally, “AAA without diabetes” (AAN) patients and “AAA complicated with type 2 diabetes mellitus” (AAM) patients had different cytokine expression patterns in their plasma, and nine plasma proteins were differentially expressed among the AAN, AAM, and HC subjects. Delta-like protein 1 (DLL1), receptor tyrosine-protein kinase erbB-3 (ERBB3), and dipeptidyl peptidase 4 (DPPIV) were significantly higher in AAM than in AAN. This study identified several promising plasma biomarkers of AAA. Their role as therapeutic targets for AAA warrants further investigation. MDPI 2022-12-12 /pmc/articles/PMC9775419/ /pubmed/36551281 http://dx.doi.org/10.3390/biom12121853 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wu, Jianqiang Wang, Wei Xie, Ting Chen, Zhaoran Zhou, Lei Song, Xiaohong Kan, Haoxuan Lv, Yanze Wu, Lianglin Li, Fangda Yang, Dan Chen, Yuexin Liu, Bao Zheng, Yuehong Identification of Novel Plasma Biomarkers for Abdominal Aortic Aneurysm by Protein Array Analysis |
title | Identification of Novel Plasma Biomarkers for Abdominal Aortic Aneurysm by Protein Array Analysis |
title_full | Identification of Novel Plasma Biomarkers for Abdominal Aortic Aneurysm by Protein Array Analysis |
title_fullStr | Identification of Novel Plasma Biomarkers for Abdominal Aortic Aneurysm by Protein Array Analysis |
title_full_unstemmed | Identification of Novel Plasma Biomarkers for Abdominal Aortic Aneurysm by Protein Array Analysis |
title_short | Identification of Novel Plasma Biomarkers for Abdominal Aortic Aneurysm by Protein Array Analysis |
title_sort | identification of novel plasma biomarkers for abdominal aortic aneurysm by protein array analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775419/ https://www.ncbi.nlm.nih.gov/pubmed/36551281 http://dx.doi.org/10.3390/biom12121853 |
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