Effects of Citrus-derived Diosmetin on Melanoma: Induction of Apoptosis and Autophagy Mediated by PI3K/Akt/mTOR Pathway Inhibition
- Autores: Li j.1, Xu M.2, Wu N.2, Wu F.2, Chen J.2, Xu X.3, Tan F.1, Liu Y.1
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Afiliações:
- Shanghai Skin Disease Clinical College, The Fifth Clinical Medical College, Anhui Medical University
- Shanghai Skin Disease Hospital, Tongji University School of Medicine
- Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai Skin Disease Hospital
- Edição: Volume 25, Nº 13 (2025)
- Páginas: 921-933
- Seção: Chemistry
- URL: https://kld-journal.fedlab.ru/1871-5206/article/view/694434
- DOI: https://doi.org/10.2174/0118715206360266250115065234
- ID: 694434
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Texto integral
Resumo
Background:Diosmetin (DIOS) is a naturally abundant flavonoid and possesses various biological activities that hold promise as an anti-cancer agent. However, the anti-cancer activities and underlying mechanism of DIOS on cutaneous melanoma remain unclear.
Objective:This study seeks to explore the anti-tumor effect and mechanism of DIOS in cutaneous melanoma.
Methods:Here, a variety of in vitro and in vivo experiments, combined with RNA sequencing (RNA-seq), were employed to ascertain the potential anti-cutaneous melanoma capacity and mechanism of DIOS.
Results:The results demonstrated that DIOS considerably impeded cell proliferation and triggered cell apoptosis in a dose- and time-dependent manner. Concurrently, DIOS markedly elevated the expression of pro-apoptotic proteins (Cleaved caspase-3, Bax, Cleaved PARP, and Cleaved caspase-9) and downregulated the expression of Bcl-2. Additionally, DIOS markedly upregulated the protein expressions of LC3B-II and Atg5, while downregulating p62 protein expression. Notably, pre-treatment with an autophagy inhibitor significantly inhibited DIOSinduced cell apoptosis and autophagy. Mechanistically, DIOS was identified to repress the PI3K/Akt/mTOR signaling pathway by western blot analyses and RNA-seq. Finally, in vivo experiments using a syngeneic mouse model confirmed the anti-tumor effect of DIOS, which exhibited high levels of apoptosis and autophagy.
Conclusion:These findings propose that DIOS acts as a potential melanoma therapy that exerts its anti-tumor effects by triggering apoptosis and autophagy via inhibition of the PI3K/Akt/mTOR pathway.
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Sobre autores
jie Li
Shanghai Skin Disease Clinical College, The Fifth Clinical Medical College, Anhui Medical University
Email: info@benthamscience.net
Mingyuan Xu
Shanghai Skin Disease Hospital, Tongji University School of Medicine
Email: info@benthamscience.net
Nanhui Wu
Shanghai Skin Disease Hospital, Tongji University School of Medicine
Email: info@benthamscience.net
Fei Wu
Shanghai Skin Disease Hospital, Tongji University School of Medicine
Email: info@benthamscience.net
Jiashe Chen
Shanghai Skin Disease Hospital, Tongji University School of Medicine
Email: info@benthamscience.net
Xiaoxiang Xu
Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai Skin Disease Hospital
Autor responsável pela correspondência
Email: info@benthamscience.net
Fei Tan
Shanghai Skin Disease Clinical College, The Fifth Clinical Medical College, Anhui Medical University
Autor responsável pela correspondência
Email: info@benthamscience.net
Yeqiang Liu
Shanghai Skin Disease Clinical College, The Fifth Clinical Medical College, Anhui Medical University
Autor responsável pela correspondência
Email: info@benthamscience.net
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