Endogenous Magnetic Lipid Droplet-Mediated Cascade-Targeted Sonodynamic Therapy as an Approach to Reversing Breast Cancer Multidrug Resistance.

IF 15.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY ACS Nano Pub Date : 2024-10-22 Epub Date: 2024-10-10 DOI:10.1021/acsnano.4c05938
Zhan Shi, Yiqing Zeng, Jiali Luo, Xue Wang, Guangrong Ma, Tao Zhang, Pintong Huang
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Abstract

Multidrug resistance (MDR) has emerged as a major barrier to effective breast cancer treatment, contributing to high rates of chemotherapy failure and disease recurrence. There is thus a pressing need to overcome MDR and to facilitate the efficient and precise treatment of breast cancer in a targeted manner. In this study, endogenous functional lipid droplets (IR780@LDs-Fe3O4/OA) were developed and used to effectively overcome the limited diffusion distance of reactive oxygen species owing to their amenability to cascade-targeted delivery, thereby facilitating precise and effective sonodynamic therapy (SDT) for MDR breast cancer. Initially, IR780@LDs-Fe3O4/OA was efficiently enriched within tumor sites in a static magnetic field, achieving the visualization of tumor treatment. Subsequently, the cascade-targeted SDT combined with the Fenton effect induced lysosome membrane permeabilization and relieved lysosomal sequestration, thus elevating drug concentration at the target site. This treatment approach also suppressed ATP production, thereby inhibiting P-glycoprotein-mediated chemotherapeutic drug efflux. This cascade-targeted SDT strategy significantly increased the sensitivity of MDR cells to doxorubicin, increasing the IC50 value of doxorubicin by approximately 10-fold. Moreover, the cascade-targeted SDT also altered the gene expression profiles of MDR cells and suppressed the expression of MDR-related genes. In light of these promising results, the combination of cascade-targeted SDT and conventional chemotherapy holds great clinical promise as an effective treatment modality with excellent biocompatibility that can improve MDR breast cancer patient outcomes.

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内源性磁脂滴介导的级联靶向声动力疗法作为逆转乳腺癌多药耐药性的一种方法
多药耐药性(MDR)已成为乳腺癌有效治疗的主要障碍,导致化疗失败率和疾病复发率居高不下。因此,克服多药耐药性,促进乳腺癌高效、精准的靶向治疗迫在眉睫。本研究开发了内源性功能性脂滴(IR780@LDs-Fe3O4/OA),由于其适合级联靶向递送,可有效克服活性氧的有限扩散距离,从而促进对MDR乳腺癌进行精确有效的声动力治疗(SDT)。最初,IR780@LDs-Fe3O4/OA 在静态磁场中被有效地富集到肿瘤部位,实现了肿瘤治疗的可视化。随后,级联靶向 SDT 与芬顿效应相结合,诱导溶酶体膜通透,缓解溶酶体螯合,从而提高靶点的药物浓度。这种治疗方法还能抑制 ATP 的产生,从而抑制 P 糖蛋白介导的化疗药物外流。这种级联靶向 SDT 策略大大提高了 MDR 细胞对多柔比星的敏感性,使多柔比星的 IC50 值提高了约 10 倍。此外,级联靶向 SDT 还改变了 MDR 细胞的基因表达谱,抑制了 MDR 相关基因的表达。鉴于这些令人鼓舞的结果,级联靶向 SDT 与传统化疗的结合在临床上大有可为,它是一种有效的治疗模式,具有良好的生物相容性,可改善 MDR 乳腺癌患者的预后。
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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
期刊最新文献
A Direct Current Self-Sustained Moisture-Electric Generator with 1D/2D Hierarchical Nanostructure for Continuous Operation of Off-Grid Electronics. Atomic Manipulation to Create High-Valent Fe4+ for Efficient and Ultrastable Oxygen Evolution at Industrial-Level Current Density. Defect-Driven Evolution of Oxo-Coordinated Cobalt Active Sites with Rapid Structural Transformation for Efficient Water Oxidation. Endogenous Magnetic Lipid Droplet-Mediated Cascade-Targeted Sonodynamic Therapy as an Approach to Reversing Breast Cancer Multidrug Resistance. Unraveling the Origin of Elemental Chemical Shift and the Role of Atomic Hydrogen in a Surface Ullmann Coupling System.
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