Commentary: "Aptamer-functionalized hybrid nanoparticle for the treatment of breast cancer".

Ronise Evans
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引用次数: 0

Abstract

The major theme throughout this paper was solving the problem of multidrug resistance (MDR) in chemotherapeutic remediation for breast cancer patients by an aptamer-labeled hybrid nanoparticle to enhance selective delivery of siRNA into tumor cells and produce an enhanced knock-down of P-glycoprotein (P-gp); which was detected mainly by western blot. The primary focus of this study was to know whether labeling nanoparticles with a cancer cell specific aptamer could enhance selective delivery of siRNA into tumor cells leading to enhanced knock-down of P-glycoprotein or P-gp as compared to non-labeled nanoparticles. The goal is to minimize cancerous gene expression by silencing its mRNA. Target specificity is not only key in completing this goal, but it is also necessary regarding, biodegradability, cytotoxicity and immune response. To accomplish this goal, the design methods had to be meticulous and carefully researched and applied.

评论:“用于治疗乳腺癌的适配体功能化杂交纳米颗粒”。
本文的主要主题是解决乳腺癌患者化疗修复中的多药耐药(MDR)问题,通过适体标记的杂交纳米颗粒增强siRNA进入肿瘤细胞的选择性递送,并产生p -糖蛋白(P-gp)的增强敲除;主要采用免疫印迹法检测。本研究的主要重点是了解与未标记的纳米颗粒相比,用癌细胞特异性适配体标记纳米颗粒是否可以增强siRNA进入肿瘤细胞的选择性递送,从而增强p糖蛋白或P-gp的敲除。其目标是通过沉默其mRNA来减少癌基因的表达。靶向特异性不仅是实现这一目标的关键,而且在生物降解性、细胞毒性和免疫应答方面也是必要的。为了实现这一目标,设计方法必须细致、仔细地研究和应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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