Li Qiushi, Zhang Zhanzhan, Wu Xueyao, Zhao Yu, Liu Yang
Key Laboratory of Functional Polymer Materials of Ministry of Education, College of Chemistry, Nankai University, Tianjin 300071, China.
State Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin 300071, China.
ACS Appl Mater Interfaces. 2025 Jan 22;17(3):4480-4489. doi: 10.1021/acsami.4c15671. Epub 2025 Jan 11.
CRISPR/Cas9 (CRISPR, clustered regularly interspaced short palindromic repeats) gene editing technology represents great promise for treating glioblastoma (GBM) due to its potential to permanently eliminate tumor pathogenic genes. Unfortunately, delivering CRISPR to the GBM in a safe and effective manner is challenging. Herein, a glycosylated and cascade-responsive nanoparticle (GCNP) that can effectively cross the blood-brain barrier (BBB) and activate CRISPR/Cas9-based gene editing only in the GBM is designed. The GCNP possesses a cationic polyplex core and a glycosylated polymer layer that is capable of cascading response to low pH and high GSH concentration, so that the release of CRISPR/Cas9 only takes place after crossing the BBB and entering the GBM where the acidic tumor microenvironment and high concentration of glutathione (GSH) are present. By targeting the programmed death-ligand 1 (PD-L1) in GBM, GCNP effectively inhibited the tumor growth and greatly prolonged the survival time of GBM-bearing mice when combined with temozolomide (TMZ).
CRISPR/Cas9(CRISPR,成簇规律间隔短回文重复序列)基因编辑技术因其具有永久消除肿瘤致病基因的潜力,在治疗胶质母细胞瘤(GBM)方面展现出巨大前景。不幸的是,以安全有效的方式将CRISPR递送至GBM具有挑战性。在此,设计了一种糖基化且具有级联响应的纳米颗粒(GCNP),其能够有效穿过血脑屏障(BBB),并且仅在GBM中激活基于CRISPR/Cas9的基因编辑。GCNP具有阳离子多聚体核心和糖基化聚合物层,该层能够对低pH值和高谷胱甘肽(GSH)浓度产生级联响应,从而使CRISPR/Cas9仅在穿过BBB并进入存在酸性肿瘤微环境和高浓度谷胱甘肽(GSH)的GBM后才会释放。通过靶向GBM中的程序性死亡配体1(PD-L1),GCNP与替莫唑胺(TMZ)联合使用时可有效抑制肿瘤生长,并显著延长荷GBM小鼠的生存时间。