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载多柔比星和 siRNA 鸡尾酒的双重靶向纳米颗粒克服卵巢癌干细胞

Dual Targeted Nanoparticles for the Codelivery of Doxorubicin and siRNA Cocktails to Overcome Ovarian Cancer Stem Cells.

机构信息

Fujian Provincial Key Laboratory of Tumor Biotherapy, Fujian Medical University Cancer Hospital & Fujian Cancer Hospital, Fuzhou 350014, China.

Fujian Provincial Key Laboratory of Medical Instrument and Pharmaceutical Technology, College of Biological Science and Technology, Fuzhou University, Fuzhou 350108, China.

出版信息

Int J Mol Sci. 2023 Jul 18;24(14):11575. doi: 10.3390/ijms241411575.

Abstract

Most anticancer treatments only induce the death of ordinary cancer cells, while cancer stem cells (CSCs) in the quiescent phase of cell division are difficult to kill, which eventually leads to cancer drug resistance, metastasis, and relapse. Therefore, CSCs are also important in targeted cancer therapy. Herein, we developed dual-targeted and glutathione (GSH)-responsive novel nanoparticles (SSBPEI-DOX@siRNAs/iRGD-PEG-HA) to efficiently and specifically deliver both doxorubicin and small interfering RNA cocktails (siRNAs) (survivin siRNA, Bcl-2 siRNA and ABCG2 siRNA) to ovarian CSCs. They are fabricated via electrostatic assembly of anionic siRNAs and cationic disulfide bond crosslinking-branched polyethyleneimine-doxorubicin (SSBPEI-DOX) as a core. Interestingly, the SSBPEI-DOX could be degraded into low-cytotoxic polyethyleneimine (PEI). Because of the enrichment of glutathione reductase in the tumor microenvironment, the disulfide bond (-SS-) in SSBPEI-DOX can be specifically reduced to promote the controlled release of siRNA and doxorubicin (DOX) in the CSCs. siRNA cocktails could specifically silence three key genes in CSCs, which, in combination with the traditional chemotherapy drug DOX, induces apoptosis or necrosis of CSCs. iRGD peptides and "sheddable" hyaluronic acid (HA) wrapped around the core could mediate CSC targeting by binding with neuropilin-1 (NRP1) and CD44 to enhance delivery. In summary, the multifunctional delivery system SSBPEI-DOX@siRNAs/iRGD-PEG-HA nanoparticles displays excellent biocompatibility, accurate CSC-targeting ability, and powerful anti-CSC ability, which demonstrates its potential value in future treatments to overcome ovarian cancer metastasis and relapse. To support this work, as exhaustive search was conducted for the literature on nanoparticle drug delivery research conducted in the last 17 years (2007-2023) using PubMed, Web of Science, and Google Scholar.

摘要

大多数抗癌治疗方法只能诱导普通癌细胞死亡,而处于细胞分裂静止期的癌症干细胞(CSC)则难以杀死,这最终导致癌症药物耐药性、转移和复发。因此,CSC 在靶向癌症治疗中也很重要。在此,我们开发了双靶向和谷胱甘肽(GSH)响应的新型纳米粒子(SSBPEI-DOX@siRNAs/iRGD-PEG-HA),以有效且特异性地递送阿霉素和小干扰 RNA 鸡尾酒(siRNAs)(survivin siRNA、Bcl-2 siRNA 和 ABCG2 siRNA)至卵巢 CSC。它们是通过将带负电荷的 siRNAs 和带正电荷的二硫键交联支化聚乙烯亚胺-阿霉素(SSBPEI-DOX)静电组装为核心来制备的。有趣的是,SSBPEI-DOX 可以降解为低细胞毒性的聚乙烯亚胺(PEI)。由于肿瘤微环境中还原型谷胱甘肽(GSH)还原酶的富集,SSBPEI-DOX 中的二硫键(-SS-)可以被特异性还原,以促进 CSC 中 siRNA 和阿霉素(DOX)的控制释放。siRNA 鸡尾酒可以特异性沉默 CSC 中的三个关键基因,与传统化疗药物 DOX 联合,诱导 CSC 的凋亡或坏死。包裹在核心周围的 iRGD 肽和“可脱落”透明质酸(HA)可以通过与神经纤毛蛋白-1(NRP1)和 CD44 结合来介导 CSC 靶向,从而增强递送。总之,多功能递送系统 SSBPEI-DOX@siRNAs/iRGD-PEG-HA 纳米粒子表现出优异的生物相容性、准确的 CSC 靶向能力和强大的抗 CSC 能力,这表明它在未来克服卵巢癌转移和复发的治疗中具有潜在的价值。为了支持这项工作,我们在过去 17 年(2007-2023 年)使用 PubMed、Web of Science 和 Google Scholar 对纳米药物递送研究的文献进行了全面搜索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7adf/10380749/320e1460d4fb/ijms-24-11575-sch001.jpg

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