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Harnessing copper-palladium alloy tetrapod nanoparticle-induced pro-survival autophagy for optimized photothermal therapy of drug-resistant cancer

机译:利用铜钯合金四足动物纳米颗粒诱导的生存自噬技术优化抗癌光热疗法

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摘要

Chemo-PTT, which combines chemotherapy with photothermal therapy, offers a viable approach for the complete tumor eradication but would likely fail in drug-resistant situations if conventional chemotherapeutic agents are used. Here we show that a type of copper (Cu)-palladium (Pd) alloy tetrapod nanoparticles (TNP-1) presents an ideal solution to the chemo-PTT challenges. TNP-1 exhibit superior near-infrared photothermal conversion efficiency, thanks to their special sharp-tip structure, and induce pro-survival autophagy in a shape- and composition-dependent manner. Inhibition of autophagy with 3-methyl adenine or chloroquine has a remarkable synergistic effect on TNP-1-mediated PTT in triple-negative (4T1), drug-resistant (MCF7/MDR) and patient-derived breast cancer models, achieving a level of efficacy unattainable with TNP-2, the identically-shaped CuPd nanoparticles that have a higher photothermal conversion efficiency but no autophagy-inducing activity. Our results provide a proof-of-concept for a chemo-PTT strategy, which utilizes autophagy inhibitors instead of traditional chemotherapeutic agents and is particularly useful for eradicating drug-resistant cancer.
机译:化学疗法-PTT将化学疗法与光热疗法相结合,为彻底根除肿瘤提供了可行的方法,但如果使用常规的化学治疗剂,在耐药情况下可能会失败。在这里,我们显示了一种类型的铜(Cu)-钯(Pd)合金四脚纳米颗粒(TNP-1)为化学PTT挑战提出了理想的解决方案。 TNP-1由于其特殊的尖端结构而表现出优异的近红外光热转换效率,并以依赖形状和成分的方式诱导生存前自噬。在三阴性(4T1),耐药(MCF7 / MDR)和患者来源的乳腺癌模型中,用3-甲基腺嘌呤或氯喹抑制自噬对TNP-1介导的PTT具有显着的协同作用。 TNP-2是具有相同形状的CuPd纳米颗粒,具有较高的光热转化效率,但没有自噬诱导活性,因此无法获得TNP-2的功效。我们的结果为化学PTT策略提供了概念验证,该策略利用自噬抑制剂代替传统的化学治疗剂,对于根除耐药性癌症特别有用。

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