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A chemo/chemodynamic nanoparticle based on hyaluronic acid induces ferroptosis and apoptosis for triple-negative breast cancer therapy
被引:18
|作者:
Wang, Ning
[1
]
Zhang, Qiyu
[1
]
Wang, Zhuoya
[1
]
Liu, Yichao
[1
]
Yang, Sen
[1
]
Zhao, Xuerong
[1
]
Peng, Jinyong
[1
,2
,3
]
机构:
[1] Dalian Med Univ, Coll Pharm, Dalian 116044, Peoples R China
[2] Anhui Univ Chinese Med, Coll Pharm, Hefei 230012, Peoples R China
[3] Hubei Univ Chinese Med, Coll Pharm, Wuhan 430065, Peoples R China
关键词:
Chemo/chemodynamic therapy;
Ferroptosis/apoptosis;
Hyaluronic acid;
Controlled drugs release;
TNBC;
DRUG-DELIVERY SYSTEM;
D O I:
10.1016/j.carbpol.2024.121795
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Triple-negative breast cancer (TNBC) poses a serious threat to women's life and health due to its high malignancy, strong invasiveness, and propensity for early recurrence and metastasis. Therefore, there is an urgent need to develop a highly effective and low-toxic TNBC treatment scheme to enhance the anti-cancer efficacy and prolong the survival of patients. In this work, we designed and synthesized a chemodynamic therapy (CDT) agent (HA-Fc-Mal). The chemo/chemodynamic (CT/CDT) nanoparticle (HCM@DOX) based on hyaluronic acid induces ferroptosis and apoptotic for TNBC therapy was constructed via self-assembled of HA-Fc-Mal and doxorubicin (DOX). HCM@DOX orderly realized the TNBC targeting, controlled DOX release, GSH depletion and induce ROS erupt. In vivo and in vitro experiments confirmed that HCM@DOX inhibited the growth of 4 T1 tumors through ferroptosis and apoptosis, and the tumor inhibition rate was as high as 81.87 %. In addition, HCM@DOX significantly inhibited lung metastasis and exhibited excellent biosafety. Overall, our findings offer a new strategy for TNBC therapy using a CT/CDT nanoparticle that induces ferroptosis and apoptosis.
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页数:16
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