Insight in the (Phospho)proteome of Vascular Smooth Muscle Cells Derived From Patients With Abdominal Aortic Aneurysm Reveals Novel Disease Mechanisms

This study revealed changes in expression and phosphorylation levels of proteins involved in various processes responsible for AAA progression and development (eg, energy metabolism, ECM remodeling, actin cytoskeleton organization, contractility, intracellular communication, and cell adhesion). These newly identified proteins, phosphosites, and related kinases provide further insight into the underlying mechanism of vascular smooth muscle cell dysfunction within the aneurysmal wall. Our omics data thereby offer the opportunity to study the relevance, either as drug target or biomarker, of these proteins in AAA development.

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Publication Details

Journal
Arteriosclerosis Thrombosis and Vascular Biology
Published
2024-08-29
DOI
https://doi.org/10.1161/atvbaha.124.321087
Citations
5
Primary Topic
Aortic aneurysm repair treatments
Type
article
Field-Weighted Citation Impact
2.09
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article

Insight in the (Phospho)proteome of Vascular Smooth Muscle Cells Derived From Patients With Abdominal Aortic Aneurysm Reveals Novel Disease Mechanisms

Thang V. Pham, Jolanda van der Velden, Sander R. Piersma, Natalija Bogunovic et al.
5 citations
Arteriosclerosis Thrombosis and Vascular Biology
Aortic aneurysm repair treatments
2.09
article

Insight in the (Phospho)proteome of Vascular Smooth Muscle Cells Derived From Patients With Abdominal Aortic Aneurysm Reveals Novel Disease Mechanisms

Thang V. Pham, Jolanda van der Velden, Sander R. Piersma, Natalija Bogunovic, Alex A. Henneman, Tara A. R. van Merrienboer, Connie R. Jiménez, Karlijn B. Rombouts, Kak Khee Yeung, Jaco C. Knol
article en
5 citations

Abstract

This study revealed changes in expression and phosphorylation levels of proteins involved in various processes responsible for AAA progression and development (eg, energy metabolism, ECM remodeling, actin cytoskeleton organization, contractility, intracellular communication, and cell adhesion). These newly identified proteins, phosphosites, and related kinases provide further insight into the underlying mechanism of vascular smooth muscle cell dysfunction within the aneurysmal wall. Our omics data thereby offer the opportunity to study the relevance, either as drug target or biomarker, of these proteins in AAA development.

Arteriosclerosis Thrombosis and Vascular BiologyVol. 44(10)
Amsterdam University Medical Centers (NL), Amsterdam UMC Location Vrije Universiteit Amsterdam (NL)
Openalex Percentile: Top 12%
Aortic aneurysm repair treatments
2.09
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