Web of Science: 0 cites, Scopus: 0 cites, Google Scholar: cites,
Reduced blood EPAC1 protein levels as a marker of severe Coronary Artery Disease: The role of hypoxic foam cell-transformed smooth muscle cells
Garcia, Eduardo (Universitat Autònoma de Barcelona. Departament de Medicina)
Claudi, Lene (Institut d'Investigacions Biomèdiques de Barcelona)
La Chica Lhoëst, Maria Teresa (Institut de Recerca Sant Pau)
Polishuck, Anna (Institut d'Investigacions Biomèdiques de Barcelona)
Samouillan, Valerie (Université de Toulouse)
Benitez Amaro, Aleyda (Institut de Recerca Sant Pau)
Piñero, Janet (Universitat Pompeu Fabra)
Escolà-Gil, Joan Carles (Institut de Recerca Sant Pau)
Sabidó, Eduard (Universitat Pompeu Fabra)
Leta, Ruben (Institut de Recerca Sant Pau)
Vilades, David (Institut de Recerca Sant Pau)
Llorente Cortes, Vicenta (Institut de Recerca Sant Pau)

Data: 2025
Resum: Background: Vascular smooth muscle cells loaded with cholesterol (foam-VSMCs) play a crucial role in the progression of human atherosclerosis. Exchange Protein Directly Activated by cAMP 1 (EPAC1) is a critical protein in the regulation of vascular tone, endothelial function, and inflammation. Our objectives were to identify proteins specifically secreted by foam human coronary VSMCs (foam-hcVSMC) to evaluate their potential as circulating biomarkers for diagnosing coronary artery disease (CAD), and to ascertain the mechanisms underlying their levels in the blood of patients with CAD. Methods and Results: Differential proteomics identified EPAC1 as a differential foamhcVSMC-secreted protein. Circulating EPAC1 levels were measured by ELISA in blood from 202 patients with suspected CAD who underwent coronary computed tomography angiography (CCTA). Blood EPAC1 levels were significantly lower in CAD patients compared to controls (p < 0. 001). EPAC1 levels were reduced in both men and women with severe CAD (SIS > 4) compared to those with moderate CAD (SIS 1–4). ROC analysis identified 9. 16 ng/ml as the optimal EPAC1 cut-off for severe CAD. At this threshold, EPAC1 predicted severe CAD (SIS > 4) with 69. 6% sensitivity and 79. 4% specificity, outperforming hs-CRP and hs-TnT in predicting CAD severity. Real-time PCR and Western blot analysis revealed that human foam-SMCs under hypoxic conditions exhibited a significant reduction in EPAC1 mRNA (p = 0. 013) and protein (p < 0. 001) levels. Conclusions: These findings suggest that circulating EPAC1 protein levels lower than 9. 16 ng/mL are predictive of severe CAD in humans. Hypoxic foam-SMCs, characteristic of advanced atherosclerotic lesions, exhibit diminished production of EPAC1, potentially contributing to the decreased circulating EPAC1 levels in patients with severe CAD.
Ajuts: Instituto de Salud Carlos III PI21/01523
Instituto de Salud Carlos III FI19/00205
Ministerio de Ciencia, Innovación y Universidades FPU21/01173
Instituto de Salud Carlos III PI24/00618
Ministerio de Ciencia, Innovación y Universidades FPU22/01888
Agència de Gestió d'Ajuts Universitaris i de Recerca 2021/SGR-00834
Nota: Altres ajuts: CSIC, "Ucrania doctores 2022", UCRAN20011
Drets: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Llengua: Anglès
Document: Article ; recerca ; Versió publicada
Matèria: Coronary artery disease (CAD) ; Coronary computed tomographic angiography (CCTA) ; Human coronary vascular smooth muscle cells (hcVSMC) ; EPAC1 ; Biomarker
Publicat a: Journal of translational medicine, Vol. 23, Num. 523 (May 2025) , ISSN 1479-5876

DOI: 10.1186/s12967-025-06513-3
PMID: 40346550


18 p, 1.9 MB

El registre apareix a les col·leccions:
Documents de recerca > Documents dels grups de recerca de la UAB > Centres i grups de recerca (producció científica) > Ciències de la salut i biociències > Institut de Recerca Sant Pau
Articles > Articles de recerca
Articles > Articles publicats

 Registre creat el 2025-04-23, darrera modificació el 2025-06-12



   Favorit i Compartir