Resumen del estudio (inglés)
pathway, and these effects were reversed by the ROS scavenger N-acetylcysteine (NAC), confirming ROS-dependent suppression of this pathway. Both network pharmacology and RNA-sequencing analyses further supported PI3K/AKT as a critical regulatory node. In summary, EAO exerts potent antitumor effects against hepatocellular carcinoma by inducing mitochondrial dysfunction and apoptosis, while concurrently suppressing autophagy through ROS-mediated inhibition of the PI3K/AKT pathway. These results highlight EAO as a promising Copyright © 2026 Xu, Zhu, Zhao, Li, Xu, Yang, Wang, Long, Zhang, Cao, Huang, Li,
Traducción al español (IA · NME)
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Detalles bibliográficos
- Autores: Xu M, Zhu M, Zhao WY, Li Z, Xu K, Yang K
- Publicado en: Frontiers in pharmacology
- PMID: 42534684
- DOI: 10.3389/fphar.2026.1884083
