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肽功能化和载药的番茄丛枝矮化病毒纳米颗粒在 Shh 依赖性髓母细胞瘤小鼠模型中抑制肿瘤生长。

Peptide-Functionalized and Drug-Loaded Tomato Bushy Stunt Virus Nanoparticles Counteract Tumor Growth in a Mouse Model of Shh-Dependent Medulloblastoma.

机构信息

Laboratory of Biomedical Technologies, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, ENEA, Casaccia Research Center, Via Anguillarese 301, 00123 Rome, Italy.

Department of Agriculture and Forest Sciences (DAFNE), University of Tuscia, Via S. Camillo De Lellis, 01100 Viterbo, Italy.

出版信息

Int J Mol Sci. 2023 May 17;24(10):8911. doi: 10.3390/ijms24108911.

Abstract

Sonic hedgehog medulloblastoma (SHH-MB) accounts for 25-30% of all MBs, and conventional therapy results in severe long-term side effects. New targeted therapeutic approaches are urgently needed, drawing also on the fields of nanoparticles (NPs). Among these, plant viruses are very promising, and we previously demonstrated that tomato bushy stunt virus (TBSV), functionalized on the surface with CooP peptide, specifically targets MB cells. Here, we tested the hypothesis that TBSV-CooP can specifically deliver a conventional chemotherapeutic drug (i.e., doxorubicin, DOX) to MB in vivo. To this aim, a preclinical study was designed to verify, by histological and molecular methods, if multiple doses of DOX-TBSV-CooP were able to inhibit tumor progression of MB pre-neoplastic lesions, and if a single dose was able to modulate pro-apoptotic/anti-proliferative molecular signaling in full-blown MBs. Our results demonstrate that when DOX is encapsulated in TBSV-CooP, its effects on cell proliferation and cell death are similar to those obtained with a five-fold higher dose of non-encapsulated DOX, both in early and late MB stages. In conclusion, these results confirm that CooP-functionalized TBSV NPs are efficient carriers for the targeted delivery of therapeutics to brain tumors.

摘要

Sonic hedgehog 型髓母细胞瘤 (SHH-MB) 占所有 MB 的 25-30%,常规疗法会导致严重的长期副作用。迫切需要新的靶向治疗方法,这也借鉴了纳米颗粒 (NPs) 的领域。在这些方法中,植物病毒非常有前途,我们之前证明,番茄丛矮病毒 (TBSV) 在表面上用 CooP 肽功能化,可特异性靶向 MB 细胞。在这里,我们测试了这样一个假设,即 TBSV-CooP 可以将常规化疗药物(即阿霉素,DOX)特异性递送至体内的 MB。为此,设计了一项临床前研究,通过组织学和分子方法验证,多剂量 DOX-TBSV-CooP 是否能够抑制 MB 前瘤病变的肿瘤进展,以及单剂量是否能够调节完全形成的 MB 中的促凋亡/抗增殖分子信号。我们的结果表明,当 DOX 被封装在 TBSV-CooP 中时,其对细胞增殖和细胞死亡的影响与非封装 DOX 的五倍更高剂量所获得的影响相似,无论是在早期还是晚期 MB 阶段。总之,这些结果证实 CooP 功能化的 TBSV NPs 是将治疗药物靶向递送至脑肿瘤的有效载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb03/10219057/e01913d331ed/ijms-24-08911-g001.jpg

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