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层状镧系元素纳米颗粒作为新型 miRNA 治疗药物的递送平台。

Layered gadolinium-based nanoparticle as a novel delivery platform for microRNA therapeutics.

机构信息

Department of Radiation Oncology, Cross Cancer Institute, Edmonton, Alberta, Canada.

出版信息

Nanotechnology. 2014 Oct 24;25(42):425102. doi: 10.1088/0957-4484/25/42/425102. Epub 2014 Oct 3.

DOI:10.1088/0957-4484/25/42/425102
PMID:25277286
Abstract

Specific expression patterns of microRNA (miRNA) molecules have been linked to cancer initiation, progression, and metastasis. The accumulating evidence for the role of oncogenic or tumor-suppressing miRNAs identified the need for nano-scaled platform that can help deliver nucleotides to modulate miRNAs. Here we report the synthesis of novel layered gadolinium hydroxychloride (LGdH) nanoparticles, a member of the layered double hydroxide (LDH) family, with physiochemical properties suitable for cell uptake and tracing via magnetic resonance (MR) imaging. As a proof of concept, we demonstrate the inhibition of mature miRNA-10b in metastatic breast cancer cell line using LGdH nanoparticle as a delivery platform. Through characterization analysis, we show that nanoparticles are easily and stably loaded with anti-miRNA oligonucleotides (AMO) and efficiently penetrate cell membranes. We demonstrate that AMOs delivered by LGdH nanoparticles remain functional by inducing changes in the expression of its downstream effector and by curbing the invasive properties. Furthermore, we demonstrate the traceability of LGdH nanoparticles via T1 weighted MR imaging. LGdH nanoparticles, which are biocompatible with cells in vitro, provide a promising multifunctional platform for microRNA therapeutics through their diagnostic, imaging, and therapeutic potentials.

摘要

特定的 microRNA(miRNA)分子的表达模式与癌症的发生、进展和转移有关。越来越多的证据表明致癌或肿瘤抑制 miRNA 的作用,这就需要一种纳米级的平台,可以帮助输送核苷酸来调节 miRNA。在这里,我们报告了新型层状钆氢氧化物(LGdH)纳米粒子的合成,它是层状双氢氧化物(LDH)家族的一员,具有适合细胞摄取和通过磁共振(MR)成像进行跟踪的物理化学性质。作为概念验证,我们使用 LGdH 纳米粒子作为递送平台,抑制了转移性乳腺癌细胞系中成熟 miRNA-10b 的表达。通过特性分析,我们表明纳米粒子可以很容易地稳定地负载抗 miRNA 寡核苷酸(AMO),并有效地穿透细胞膜。我们证明,LGdH 纳米粒子递送的 AMO 通过诱导其下游效应物的表达变化并抑制侵袭性来保持其功能。此外,我们通过 T1 加权磁共振成像证明了 LGdH 纳米粒子的可追踪性。LGdH 纳米粒子在体外与细胞具有生物相容性,通过其诊断、成像和治疗潜力,为 miRNA 治疗提供了一种有前途的多功能平台。

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