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脂质体-丙咪嗪蓝在体内抑制音猬因子型髓母细胞瘤

Liposome-Imipramine Blue Inhibits Sonic Hedgehog Medulloblastoma In Vivo.

作者信息

MacDonald Tobey J, Liu Jingbo, Yu Bing, Malhotra Anshu, Munson Jenny, Park Jaekeun C, Wang Kenty, Fei Baowei, Bellamkonda Ravi, Arbiser Jack

机构信息

Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30329, USA.

Aflac Cancer & Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, GA 30329, USA.

出版信息

Cancers (Basel). 2021 Mar 11;13(6):1220. doi: 10.3390/cancers13061220.

DOI:10.3390/cancers13061220
PMID:33799550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8001973/
Abstract

Sonic hedgehog subtype of medulloblastoma (SHH MB) with metastasis or specific clinical or molecular alteration shas a poor prognosis and current therapy results in long-term cognitive impairment in the majority of survivors. Thus, a great need exists for new targeted therapeutic approaches to more effectively treat SHH MB in children. Imipramine blue (IB), a novel molecule with anti-tumor properties, inhibits the NADPH oxidase (NOX) family of enzymes, which are critical for SHH MB survival and treatment resistance. In this study, IB was encapsulated within a liposome to form a liposomal nanoparticle, Liposome-IB (Lipo-IB). This complex has the ability to cross the blood-brain barrier and be preferentially taken up by tumor cells within the brain. We demonstrated in vitro that Lipo-IB treatment caused a dose-dependent decrease in SHH MB cell viability and migration. Short-term administration of single agent Lipo-IB treatment of SHH MB in vivo significantly inhibited tumor growth, reduced the tumor volume, including a complete tumor response, and improved survival compared to control treated mice, without any observable toxicity. We conclude that Lipo-IB is a potential novel nanoparticle-based therapeutic for the treatment of SHH MB that warrants further preclinical safety and efficacy testing for development towards clinical investigation.

摘要

具有转移或特定临床或分子改变的髓母细胞瘤的音猬因子亚型(SHH MB)预后较差,目前的治疗方法会导致大多数幸存者出现长期认知障碍。因此,迫切需要新的靶向治疗方法来更有效地治疗儿童SHH MB。亚甲蓝(IB)是一种具有抗肿瘤特性的新型分子,可抑制NADPH氧化酶(NOX)家族的酶,这些酶对SHH MB的存活和治疗耐药性至关重要。在本研究中,IB被包裹在脂质体内形成脂质体纳米颗粒,即脂质体-IB(Lipo-IB)。这种复合物能够穿过血脑屏障,并被脑内的肿瘤细胞优先摄取。我们在体外证明,Lipo-IB处理导致SHH MB细胞活力和迁移呈剂量依赖性下降。与对照处理的小鼠相比,在体内对SHH MB进行单药Lipo-IB的短期给药显著抑制了肿瘤生长,减小了肿瘤体积,包括完全肿瘤反应,并提高了生存率,且没有任何可观察到的毒性。我们得出结论,Lipo-IB是一种潜在的基于纳米颗粒的新型SHH MB治疗药物,值得进一步进行临床前安全性和有效性测试,以推进临床研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/650a7838db26/cancers-13-01220-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/a1775cfc231e/cancers-13-01220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/8cf40d8f700f/cancers-13-01220-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/eb8301729197/cancers-13-01220-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/c983427d6b3b/cancers-13-01220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/7aa8f97b16e9/cancers-13-01220-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/650a7838db26/cancers-13-01220-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/a1775cfc231e/cancers-13-01220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/8cf40d8f700f/cancers-13-01220-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/eb8301729197/cancers-13-01220-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/c983427d6b3b/cancers-13-01220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/7aa8f97b16e9/cancers-13-01220-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53b/8001973/650a7838db26/cancers-13-01220-g006.jpg

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