Short interfering RNA delivered by a hybrid nanoparticle targeting VEGF: Biodistribution and anti-tumor effect

纳米载体 体内 小干扰RNA 基因沉默 癌症研究 材料科学 RNA干扰 纳米颗粒 体内分布 癌症 小发夹RNA 纳米技术 化学 核糖核酸 医学 生物 内科学 基因 生物化学 生物技术
作者
Gabriela Regina Rosa Souza,Milene Dalmina,Jelver A. Sierra,Leônidas João de Mello,Adny Henrique Silva,Ana Cristina Moura Gualberto,Jacy Gameiro,Dalton Dittz,André A. Pasa,Frederico Pittella,Tânia Beatriz Creczynski-Pasa
出处
期刊:Biochimica Et Biophysica Acta - General Subjects [Elsevier BV]
卷期号:1865 (9): 129938-129938 被引量:5
标识
DOI:10.1016/j.bbagen.2021.129938
摘要

The use of RNA interference (iRNA) therapy has proved to be an interesting target therapy for the cancer treatment; however, siRNAs are unstable and quickly eliminated from the bloodstream. To face these barriers, the use of biocompatible and efficient nanocarriers emerges as an alternative to improve the success application of iRNA to the cancer, including breast cancer.A hybrid nanocarrier composed of calcium phosphate as the inorganic phase and a block copolymer containing polyanions as organic phase, named HNPs, was developed to deliver VEGF siRNA into metastatic breast cancer in mice. The particles presented a rounded shape by TEM images with average size measured by DLS suitable and biocompatible for biomedical applications. The XPS and EDS spectra confirmed the hybrid composition of the nanoparticles. Moreover, after intravenous administration, the particles accumulated mainly in the tumor site and kidneys, which demonstrates the tumor targeting accumulation through the Enhanced Permeability and Retention Effect (EPR). A significant decrease in size of the tumors treated with the nanoparticles containing siVEGF (HNPs-siVEGF) was observed and the reduction was related to enhanced tumor accumulation of siRNA as well as in vivo VEGF silencing at gene and protein levels.The hybrid system prepared was successful in promoting the RNAi effect in vivo with very low toxicity.This study shows the valuable development of a hybrid nanoparticle carrying VEGF siRNA, as well as their tumor targeting, accumulation and reduction in mice triple-negative breast cancer.
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