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Novel gene therapy CM-YAPon protects the mouse heart from myocardial infarction - MI

GSE293327 Mus musculus Expression profiling by high throughput sequencing 4 samples Submitted 2025/09/30 Platform GPL34290
Summary
Myocardial infarction (MI), which affects about 3 million people globally each year, permanently damages the heart and reduces cardiac function1. Recent studies have indicated that activating YAP in cardiomyocytes (CMs) promotes cardiac regeneration and mitigates pathological remodeling in mouse and pig MI models2,3. To precisely control YAP activity in vivo and encourage its clinical application, we developed an adeno-associated virus 9 (AAV9)-based therapy, termed CM-YAPon, which triggers YAP activation in CMs upon exposure to a small molecule LMI070. One dose of LMI070 in mice induced a transient expression of active YAP (YAP5SA), which was subsequently degraded within a week. Consistent with earlier findings, YAP activation after injury improved cardiac function. Interestingly, administering a single LMI070 injection two weeks before MI provided lasting cardioprotection, which diminished by four weeks after the transient YAP activation, by reducing non-CMs cell death and enhancing cardiac function. Taken together, our novel gene therapy CM-YAPon presents a promising avenue for developing protective strategies against MI-induced cardiac injury.
Published in
Gene therapy CM-YAP(on) protects the mouse heart from myocardial infarction
Meng F, Steimle JD, Straight E et al. · Nature cardiovascular research 2025 · PMID 41233538 · doi:10.1038/s44161-025-00744-9
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Also filed as BioProject PRJNA1244144 and SRA study SRP575251. Searching any of these in the dataset finder brings you back here.

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