4.6 Article

TCF7L1 Accelerates Smooth Muscle Cell Phenotypic Switching and Aggravates Abdominal Aortic Aneurysms

Journal

JACC-BASIC TO TRANSLATIONAL SCIENCE
Volume 8, Issue 2, Pages 155-170

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacbts.2022.07.012

Keywords

KEY WORDS abdominal aortic aneurysms; phenotypic switching; smooth muscle cell

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Phenotypic switching of vascular smooth muscle cells plays a central role in abdominal aortic aneurysm pathology. Knockdown of TCF7L1 inhibits the differentiation of vascular smooth muscle cells. This study suggests potential interventions to prevent AAA by maintaining a normal differentiated smooth muscle cell state, and TCF7L1 may serve as a biomarker for AAA.
Phenotypic switching of vascular smooth muscle cells is a central process in abdominal aortic aneurysm (AAA) pathology. We found that knockdown TCF7L1 (transcription factor 7-like 1), a member of the TCF/LEF (T cell factor/lymphoid enhancer factor) family of transcription factors, inhibits vascular smooth muscle cell differ-entiation. This study hints at potential interventions to maintain a normal, differentiated smooth muscle cell state, thereby eliminating the pathogenesis of AAA. In addition, our study provides insights into the potential use of TCF7L1 as a biomarker for AAA. (J Am Coll Cardiol Basic Trans Science 2023;8:155-170) & COPY; 2023 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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