College of Pharmacy, Dalian Medical University, Dalian 116044, China.
College of Pharmacy, Dalian Medical University, Dalian 116044, China.
Carbohydr Polym. 2024 Apr 1;329:121795. doi: 10.1016/j.carbpol.2024.121795. Epub 2024 Jan 9.
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.
三阴性乳腺癌(TNBC)由于其高恶性度、强侵袭性、早期复发和转移倾向,对女性的生命和健康构成严重威胁。因此,迫切需要开发一种高效低毒的 TNBC 治疗方案,以提高抗癌疗效,延长患者的生存时间。在本工作中,我们设计并合成了一种化学动力学治疗(CDT)剂(HA-Fc-Mal)。基于透明质酸的化疗/化学动力学(CT/CDT)纳米颗粒(HCM@DOX)通过 HA-Fc-Mal 和阿霉素(DOX)的自组装构建,用于 TNBC 治疗。HCM@DOX 有序地实现了 TNBC 的靶向、控制 DOX 的释放、GSH 的耗竭和诱导 ROS 的爆发。体内外实验证实,HCM@DOX 通过铁死亡和细胞凋亡抑制了 4T1 肿瘤的生长,肿瘤抑制率高达 81.87%。此外,HCM@DOX 还显著抑制了肺转移,并表现出优异的生物安全性。总之,我们的研究结果为使用诱导铁死亡和细胞凋亡的 CT/CDT 纳米颗粒治疗 TNBC 提供了一种新策略。