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超声诱导金纳米颗粒联合巨噬细胞声学重编程用于增强癌症治疗

Ultrasound-Induced Gold Nanoparticle United with Acoustic Reprogramming of Macrophages for Enhanced Cancer Therapy.

作者信息

Tang Qinchao, Zhang Fanyu, Luo Licheng, Duan Yiling, Zhu Taomin, Ni Yueqi, Wang Yang, Qi Haoning, Jiang Shuting, Zhou Jingxuan, Ma Xiaoxin, Zhang Yufeng

机构信息

State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan 430079, China.

Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education and School of Physics and Technology, Wuhan University, Wuhan 430079, China.

出版信息

ACS Appl Mater Interfaces. 2023 Oct 25. doi: 10.1021/acsami.3c12599.

Abstract

Sonodynamic therapy (SDT) has considerable potential in cancer treatment and exhibits high tissue penetration with minimal damage to healthy tissues. The efficiency of SDT is constrained by the complex immunological environment and tumor treatment resistance. Herein, a specific acoustic-actuated tumor-targeted nanomachine is proposed to generate mechanical damage to lysosomes for cancer SDT. The hybrid nanomachine was assembled with gold nanoparticles (GNPs) as the core and encapsulated with macrophage exosomes modified by AS1411 aptamers (GNP@EXO-APs) to optimize the pharmacokinetics and tumor aggregation. GNP@EXO-APs could be specifically transferred to the lysosomes of tumor cells. After induction with ultrasound, GNP@EXO-APs generated strong mechanical stress to produce lysosomal-dependent cell death in cancer cells. Notably, tumor-associated macrophages were reprogrammed in the ultrasound environment to an antitumor phenotype. Enhanced mechanical destruction via GNP@EXO-APs and immunotherapy of cancer cells were verified both in vitro and in vivo under SDT. This study provides a new direction for inside-out killing effects on tumor cells for cancer treatment.

摘要

声动力疗法(SDT)在癌症治疗中具有巨大潜力,且对健康组织损伤最小,组织穿透性高。SDT的效率受到复杂免疫环境和肿瘤治疗抗性的限制。在此,我们提出一种特定的声学驱动肿瘤靶向纳米机器,用于对溶酶体产生机械损伤以进行癌症SDT。这种混合纳米机器以金纳米颗粒(GNPs)为核心组装而成,并包裹有经AS1411适配体修饰的巨噬细胞外泌体(GNP@EXO-APs),以优化药代动力学和肿瘤聚集。GNP@EXO-APs能够特异性转移至肿瘤细胞的溶酶体。在超声诱导后,GNP@EXO-APs产生强大的机械应力,导致癌细胞发生溶酶体依赖性细胞死亡。值得注意的是,肿瘤相关巨噬细胞在超声环境中被重编程为抗肿瘤表型。在SDT条件下,通过GNP@EXO-APs增强机械破坏以及对癌细胞进行免疫治疗,在体外和体内均得到了验证。本研究为癌症治疗中对肿瘤细胞进行由内而外的杀伤作用提供了新方向。

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