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Natural product nanozymes of herbal extract galangin in managing hepatocellular carcinoma.
Wang, Erhao; Wu, Yuxia; Wang, Yan; Li, Jiao; Liang, Xiuzhen; Wang, Zhongtao; Liu, Xiaofei; Feng, Faming; Mao, JianCang; Zhu, Yingqi; Li, Le.
Affiliation
  • Wang E; Hainan Women and Children's Medical Center, Haikou, China.
  • Wu Y; Hainan General Hospital/Hainan Affiliated Hospital of Hainan Medical University, Haikou, China.
  • Wang Y; Hainan Women and Children's Medical Center, Haikou, China.
  • Li J; Hainan Women and Children's Medical Center, Haikou, China.
  • Liang X; Hainan Women and Children's Medical Center, Haikou, China.
  • Wang Z; Hainan Women and Children's Medical Center, Haikou, China.
  • Liu X; Hainan Women and Children's Medical Center, Haikou, China.
  • Feng F; Hainan Women and Children's Medical Center, Haikou, China.
  • Mao J; NHC (National Health Commission of the People's Republic of China) Key Laboratory of Tropical Disease Control, School of Tropical Medicine, Hainan Medical University, Haikou, Hainan, China.
  • Zhu Y; NHC (National Health Commission of the People's Republic of China) Key Laboratory of Tropical Disease Control, School of Tropical Medicine, Hainan Medical University, Haikou, Hainan, China.
  • Li L; NHC (National Health Commission of the People's Republic of China) Key Laboratory of Tropical Disease Control, School of Tropical Medicine, Hainan Medical University, Haikou, Hainan, China.
Front Chem ; 12: 1426634, 2024.
Article de En | MEDLINE | ID: mdl-38915904
ABSTRACT
Numerous local herbal extract species have been investigated as potential medicinal ingredients due to their promising anti-cancer properties. However, the primary constraint of the class of plant flavonoids lies in their low solubility and limited membrane permeability, leading to chemical instability and restricted bioavailability that impede biomedical applications. In this study, we have developed an ideal nanozyme-Galazyme, comprising galangin-loaded copper Nanozyme coated by DSPE-PEG, which amplifies oxidative stress to induce apoptosis via the regulation of reactive oxygen species (ROS) generation and mitogen-activated protein kinase (MAPK) activation. Galazyme exhibited significant peroxidase mimetic activity, demonstrating its potential to generate ROS and elevate oxidative stress. Upon uptake by HepG-2 cells, Galazyme efficiently converts excess hydrogen peroxide (H2O2) into highly reactive •OH radicals and upregulates MAPK expression, leading to the activation of Bax and Caspase 3, thereby promoting irreversible tumor cell apoptosis. Both in vitro and in vivo results demonstrate that Galazyme inhibits tumor cell growth and induces apoptosis by generating ample ROS and activating the MAPK pathway. Our study offers novel evidence supporting the enhancement of Galazyme-induced apoptosis through the upregulation of Bax and Caspase 3, along with the elucidation of the interaction between MAPK and apoptosis.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Front Chem Année: 2024 Type de document: Article Pays d'affiliation: Chine

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Front Chem Année: 2024 Type de document: Article Pays d'affiliation: Chine