Suppr超能文献

通过 GPC3 靶向协同化疗-光热治疗促进肝细胞癌的早期诊断和精准治疗。

Promoting Early Diagnosis and Precise Therapy of Hepatocellular Carcinoma by Glypican-3-Targeted Synergistic Chemo-Photothermal Theranostics.

机构信息

Department of Pharmaceutics, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences , Shandong University , 44 Wenhua Xi Road , Jinan , Shandong Province 250012 , People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2019 Jul 3;11(26):23591-23604. doi: 10.1021/acsami.9b05526. Epub 2019 Jun 19.

Abstract

The specific-targeting approach could promote the specificity of diagnosis and the accuracy of cancer treatment. The choice of a specific-targeting receptor is the key step in this approach. Glypican-3 (GPC3) is an oncofetal proteoglycan anchored on the cell membrane. It is overexpressed even in the early stage of hepatocellular carcinoma (HCC), whereas it shows almost no expression in the healthy adult liver. Therefore, GPC3 may be applied as a specific-targeting receptor for HCC theranostics. In this study, a GPC3 specific-targeting theranostics nanodevice, GPC3 targeting peptide (named G12)-modified liposomes co-loaded with sorafenib (SF) and IR780 iodide (IR780), was developed (GSI-Lip), which aims to realize early diagnosis and precise chemo-photothermal therapy of HCC. SF was the first-line chemotherapy drug for the treatment of HCC. IR780 was used for photothermal therapy and near-infrared fluorescence imaging. The evaluation of early diagnosis verified that early-stage tumors (3.45 ± 0.98 mm, 2 days after 5 × 10 H22 cells' inoculation in mice) could be clearly detected using GSI-Lip, which was significantly more sensitive than folic acid-modified liposomes ( p < 0.01, 32.90 ± 10.01 mm, 4 days after 1 × 10 H22 cells' inoculation in mice). The study of the endocytic pathway indicated that specific G12/GPC3 recognition may induce caveolae-mediated endocytosis of GSI-Lip. Notably, the accumulation of GSI-Lip in tumors was significantly increased compared with that observed with folic acid-modified liposomes ( p < 0.01). Specific-targeting endowed the precise antitumor effect of GSI-Lip. GSI-Lip showed a higher antitumor efficacy in comparison with folic acid-modified liposomes (inhibition rate: 90.52% vs 84.22%, respectively; p < 0.01). During a period of 21 days, the synergistic chemo-photothermal therapy (GSI-Lip + laser) exhibited a better antitumor effect versus GSI-Lip without laser (inhibition rate: 94.93% vs 90.52%, respectively; p < 0.01). Overall, GPC3-targeted GSI-Lip promoted the sensitivity and specificity of HCC early diagnosis and achieved synergistic efficacy of chemo-photothermal theranostics, which has potential clinical applications. Furthermore, the present study revealed that a more specific-targeting ligand could further improve the efficacy of theranostics against HCC.

摘要

靶向特定受体的方法可以提高诊断的特异性和癌症治疗的准确性。选择特定的靶向受体是这种方法的关键步骤。磷脂酰聚糖-3(GPC3)是一种锚定在细胞膜上的癌胚蛋白聚糖。即使在肝癌(HCC)的早期阶段,它也过度表达,而在健康成人肝脏中几乎没有表达。因此,GPC3 可作为 HCC 治疗的特异性靶向受体。在这项研究中,开发了一种 GPC3 特异性靶向治疗纳米装置,即 GPC3 靶向肽(命名为 G12)修饰的脂质体共载索拉非尼(SF)和 IR780 碘化物(IR780)(GSI-Lip),旨在实现 HCC 的早期诊断和精确化疗-光热治疗。SF 是治疗 HCC 的一线化疗药物。IR780 用于光热治疗和近红外荧光成像。早期诊断的评估证实,早期肿瘤(接种小鼠 5×10 H22 细胞后 2 天,3.45±0.98mm)可以用 GSI-Lip 清楚地检测到,这明显比叶酸修饰的脂质体更敏感(p<0.01,接种小鼠 1×10 H22 细胞后 4 天,32.90±10.01mm)。内吞途径的研究表明,特异性 G12/GPC3 识别可能诱导 GSI-Lip 的小窝介导内吞作用。值得注意的是,与叶酸修饰的脂质体相比,GSI-Lip 在肿瘤中的积累明显增加(p<0.01)。特异性靶向赋予了 GSI-Lip 精确的抗肿瘤作用。GSI-Lip 与叶酸修饰的脂质体相比具有更高的抗肿瘤疗效(抑制率:分别为 90.52%和 84.22%;p<0.01)。在 21 天的时间内,协同化疗-光热治疗(GSI-Lip+激光)与无激光的 GSI-Lip 相比具有更好的抗肿瘤效果(抑制率:分别为 94.93%和 90.52%;p<0.01)。总的来说,GPC3 靶向 GSI-Lip 提高了 HCC 早期诊断的灵敏度和特异性,并实现了化疗-光热治疗的协同疗效,具有潜在的临床应用价值。此外,本研究表明,更特异性的靶向配体可以进一步提高 HCC 治疗的疗效。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验