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双波变性能量纳米诊疗剂用于癌症的双模成像引导光诱导的三重治疗。

Two-Wave Variable Nanotheranostic Agents for Dual-Mode Imaging-Guided Photo-Induced Triple-Therapy for Cancer.

机构信息

Department of Pharmaceutics, Key Laboratory of Chemical Biology (Ministry of Education), NMPA Key Laboratory for Technology Research and Evaluation of Drug Products, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, 44 Wenhua Xi Road, Jinan, Shandong Province, 250012, China.

Department of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, 324 Jingwu Weiqi Road, Jinan, Shandong Province, 250021, China.

出版信息

Adv Sci (Weinh). 2022 Sep;9(27):e2201834. doi: 10.1002/advs.202201834. Epub 2022 Aug 2.

Abstract

Photothermal therapy (PTT) is a promising strategy for cancer treatment, but its clinical application relies heavily on accurate tumor positioning and effective combination. Nanotheranostics has shown superior application in precise tumor positioning and treatment, bringing potential opportunities for developing novel PTT-based therapies. Here, a nanotheranostic agent is proposed to enhance magnetic resonance imaging (MRI)/ near-infrared fluorescence imaging (NIRFI) imaging-guided photo-induced triple-therapy for cancer. Thermosensitive liposomes co-loaded with SPIONs/IR780 and Abemaciclib (SIA-TSLs), peptide ACKFRGD, and click group 2-cyano-6-amino-benzothiazole (CABT) are co-modified on the surface of SIA-TSLs to form SIA-αTSLs. ACKFRGD can be hydrolyzed to expose the 1, 2-thiolamino groups in the presence of cathepsin B in tumors, which click cycloaddition with the cyano group on CABT, resulting in the formation of SIA-αTSLs aggregates. The aggregation of SIA-αTSLs in tumors enhances the MRI/NIRFI imaging capability and enables precise PTT. Photo-induced triple-therapy enhances precision cancer therapy. First, PTT ablates specific tumors and induces ICD via localized photothermal. Second, local tumor heating promotes the rupture of SIA-αTSLs, which release Abemaciclib to block the tumor cell cycle and inhibit Tregs proliferation. Third, injecting GM-CSF into tumor tissue leads to recruitment of dendritic cells and initiation of antitumor immunity. Collectively, these results present a promising nanotheranostic strategy for future cancer therapy.

摘要

光热治疗(PTT)是一种有前途的癌症治疗策略,但它的临床应用严重依赖于肿瘤的精确定位和有效结合。纳米诊疗在精确肿瘤定位和治疗方面显示出了卓越的应用,为开发新型基于 PTT 的治疗方法带来了潜在的机会。在这里,提出了一种纳米诊疗剂,以增强磁共振成像(MRI)/近红外荧光成像(NIRFI)成像引导的光诱导三重治疗癌症。载有 SPIONs/IR780 和 Abemaciclib(SIA-TSLs)的热敏脂质体,肽 ACKFRGD,和点击基团 2-氰基-6-氨基苯并噻唑(CABT)共同修饰在 SIA-TSLs 的表面,形成 SIA-αTSLs。在肿瘤中存在组织蛋白酶 B 的情况下,ACKFRGD 可以被水解,暴露出 1,2-硫醇基,然后与 CABT 上的氰基发生点击环加成反应,导致 SIA-αTSLs 聚集。SIA-αTSLs 在肿瘤中的聚集增强了 MRI/NIRFI 成像能力,并实现了精确的 PTT。光诱导三重治疗增强了精确癌症治疗。首先,PTT 通过局部光热消融特定的肿瘤并诱导 ICD。其次,局部肿瘤加热促进 SIA-αTSLs 的破裂,释放 Abemaciclib 以阻断肿瘤细胞周期并抑制 Tregs 增殖。第三,向肿瘤组织中注射 GM-CSF 导致树突状细胞的募集和抗肿瘤免疫的启动。总之,这些结果为未来的癌症治疗提供了一种有前途的纳米诊疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ea4/9507363/eec3fa9c4992/ADVS-9-2201834-g002.jpg

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