Multifunctional iron-apigenin nanocomplex conducting photothermal therapy and triggering augmented immune response for triple negative breast cancer

光热治疗 免疫系统 三阴性乳腺癌 乳腺癌 纳米壳 肿瘤微环境 癌症研究 免疫原性细胞死亡 癌症 医学 癌细胞 化学 免疫学 纳米技术 免疫疗法 材料科学 内科学 纳米颗粒
作者
Ruijie Chen,Zewei Jiang,Yingfeng Cheng,Jinyao Ye,Shize Li,Yitianhe Xu,Zhanzheng Ye,Yifan Shi,Jie Ding,Yingyi Zhao,Hailun Zheng,Fu‐Gen Wu,Guangyong Lin,Congying Xie,Qing Yao,Longfa Kou
出处
期刊:International Journal of Pharmaceutics [Elsevier BV]
卷期号:655: 124016-124016 被引量:12
标识
DOI:10.1016/j.ijpharm.2024.124016
摘要

Triple negative breast cancer (TNBC) presents a formidable challenge due to its low sensitivity to many chemotherapeutic drugs and a relatively low overall survival rate in clinical practice. Photothermal therapy has recently garnered substantial interest in cancer treatment, owing to its swift therapeutic effectiveness and minimal impact on normal cells. Metal-polyphenol nanostructures have recently garnered significant attention as photothermal transduction agents due to their facile preparation and favorable photothermal properties. In this study, we employed a coordinated approach involving Fe3+ and apigenin, a polyphenol compound, to construct the nanostructure (nFeAPG), with the assistance of β-CD and DSPE-PEG facilitating the formation of the complex nanostructure. In vitro research demonstrated that the formed nFeAPG could induce cell death by elevating intracellular oxidative stress, inhibiting antioxidative system, and promoting apoptosis and ferroptosis, and near infrared spectrum irradiation further strengthen the therapeutic outcome. In 4T1 tumor bearing mice, nFeAPG could effectively accumulate into tumor site and exhibit commendable control over tumor growth. Futher analysis demonstrated that nFeAPG ameliorated the suppressed immune microenvironment by augmenting the response of DC cells and T cells. This study underscores that nFeAPG encompasses a multifaceted capacity to combat TNBC, holding promise as a compelling therapeutic strategy for TNBC treatment.
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