SCH79797, an Antiplatelet Agent, Alleviates Restenosis by Inducing Apoptosis via p53-Mediated Mitochondrial Depolarization and Inhibiting Thrombus Formation after Angioplasty
Our findings have established SCH79797 as a promising candidate for reducing ISR through apoptosis modulation. By leveraging the p53-mediated mitochondrial apoptotic pathway, SCH79797 may provide a groundbreaking approach to reducing restenosis. These findings could offer significant implications for the future development of targeted drug-eluting strategies by locally delivering SCH79797 in a controlled manner using DES or DEB, presenting SCH79797 as a transformative candidate in interventional cardiology.
Authors
- Kun‐Jing Hong (ORCID: https://orcid.org/0000-0003-4522-8423)
- Chieh‐Yu Chen (ORCID: https://orcid.org/0000-0001-8315-0781)
- Wen‐Chin Ko (ORCID: https://orcid.org/0000-0002-7109-832X)
- Ting‐Lin Yen (ORCID: https://orcid.org/0000-0002-1454-0521)
- Jing‐Shiun Jan (ORCID: https://orcid.org/0000-0003-0524-113X)
- Yi‐Ling Chen (ORCID: https://orcid.org/0000-0002-9789-2441)
- Po-Ching Chou
Institutions
- Fu Jen Catholic University (TW)
- Cathay General Hospital (TW)
- Taipei Medical University (TW)
Publication Details
- Journal
- Current Molecular Medicine
- Published
- 2025-10-01
- DOI
- https://doi.org/10.2174/0115665240375398250916093346
- Citations
- 1
- Primary Topic
- Coronary Interventions and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 2.01