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线粒体介导热休克蛋白抑制策略增强低温光热治疗。

Mitochondria-Mediated HSP Inhibition Strategy for Enhanced Low-Temperature Photothermal Therapy.

机构信息

State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and KLMDASR of Tianjin, Nankai University, Tongyan Road, Haihe Education Park, Tianjin 300350, China.

出版信息

ACS Appl Mater Interfaces. 2023 Jun 7;15(22):26252-26262. doi: 10.1021/acsami.3c00870. Epub 2023 May 23.

Abstract

Low-temperature photothermal therapy (PTT) has the advantage of causing less damage to normal tissues and has attracted great attention in recent years. However, the efficacy of low-temperature PTT is restricted by the overexpression of heat shock proteins (HSPs), specifically HSP70 and HSP90. Inhibiting the function of these HSPs is a major strategy used in the development of new cancer therapies. Herein, we designed four T780T-containing thermosensitive nanoparticles to interrupt the energy supply for HSP expression using their TPP-based mitochondrial targeting action. The reversal behavior of the nanoparticles on the gambogic acid (GA)-induced compensatory increase of HSP70 was investigated by Western blot and by immunohistochemistry. The anticancer efficacy of the low-temperature PTT based on these thermosensitive nanoparticles was also systematically examined. The design proposes for the first time to utilize and elucidate the mechanism of the mitochondrial targeting of T780T-containing NPs in synergy with the HSP90 inhibition of GA to achieve an effective low-temperature PTT. This work not only provides a novel pathway for the dual inhibition of HSP70 and HSP90 but also opens up a new approach for low-temperature PTT of tumors.

摘要

低温光热疗法 (PTT) 的优点是对正常组织造成的损伤较小,近年来引起了广泛关注。然而,低温 PTT 的疗效受到热休克蛋白 (HSPs) 过度表达的限制,特别是 HSP70 和 HSP90。抑制这些 HSP 的功能是开发新癌症治疗方法的主要策略。在这里,我们设计了四种含有 T780T 的热敏纳米粒子,通过基于 TPP 的线粒体靶向作用来中断 HSP 表达的能量供应。通过 Western blot 和免疫组织化学研究了纳米粒子对 GA 诱导的 HSP70 代偿性增加的逆转行为。还系统地检查了基于这些热敏纳米粒子的低温 PTT 的抗癌功效。该设计首次提出利用并阐明含有 T780T 的 NPs 与 GA 抑制 HSP90 的线粒体靶向协同作用的机制,以实现有效的低温 PTT。这项工作不仅为 HSP70 和 HSP90 的双重抑制提供了一条新途径,也为肿瘤的低温 PTT 开辟了一条新途径。

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