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Chemokine Receptor 2 Is a Theranostic Biomarker for Abdominal Aortic Aneurysms

Title: Chemokine Receptor 2 Is a Theranostic Biomarker for Abdominal Aortic Aneurysms
Authors: Santiago Elizondo-Benedetto, MD; Sergio Sastriques-Dunlop, MD; Lisa Detering, MS; Batool Arif, MS; Gyu Seong Heo, PhD; Deborah Sultan, BS; Hannah Luehmann, MS; Xiaohui Zhang, PhD; Xuefeng Gao, PhD; Andrea Bredemeyer, PhD; Mohamed S. Zaghloul, MD; Kitty Harrison, BS; Dakkota Thies, BS; Laura McDonald, BS; Christophe Combadière, PhD; Chieh-Yu Lin, MD, PhD; Yeona Kang, PhD; Jie Zheng, PhD; Joseph Ippolito, MD, PhD; Richard Laforest, PhD; Kory Lavine, MD, PhD; Robert J. Gropler, MD; Sean J. English, MD; Mohamed A. Zayed, MD, PhD; Yongjian Liu, PhD
Source: JACC: Basic to Translational Science, Vol 10, Iss 7, Pp 101250- (2025)
Publisher Information: Elsevier
Publication Year: 2025
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: abdominal aortic aneurysm; CCR2; inflammation; theranostic; translation; Diseases of the circulatory (Cardiovascular) system; RC666-701
Description: Summary: Abdominal aortic aneurysm (AAA) is a degenerative vascular disease with a high mortality upon rupture. There is no diagnosis to predict the rupture nor effective medical therapies to prevent rupture. Here we demonstrate that the C-C chemokine receptor type 2 (CCR2) is a theranostic biomarker for AAA. In rat AAA models, we determined the potential of a CCR2-targeted positron emission tomography radiotracer [64Cu]Cu-DOTA-ECL1i predicting AAA rupture. Using a CCR2 inhibitor, we observed the effective prevention of rupture in AAA rat models. In humans, CCR2 positron emission tomography showed intense radiotracer uptake along the AAA wall in patients while little signal was observed in healthy volunteers.
Document Type: article in journal/newspaper
Language: English
Relation: http://www.sciencedirect.com/science/article/pii/S2452302X25000671; https://doaj.org/toc/2452-302X; https://doaj.org/article/36ff84107dd74ec18dfca5c4c5900049
DOI: 10.1016/j.jacbts.2025.02.010
Availability: https://doi.org/10.1016/j.jacbts.2025.02.010; https://doaj.org/article/36ff84107dd74ec18dfca5c4c5900049
Accession Number: edsbas.CD14F5
Database: BASE