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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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