State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, China.
Nanomedicine. 2019 Oct;21:102061. doi: 10.1016/j.nano.2019.102061. Epub 2019 Jul 22.
Targeted DNA nanoparticles have been identified as one of the most promising nanocarriers in anti-glioma drug delivery. We established a multifunctional nanosystem for targeted glioma therapy. Tetrahedral framework nucleic acid (tFNA), entering U87MG cells and bEnd.3 cells, was chosen to deliver two aptamers, GMT8 and Gint4.T, and paclitaxel. GMT8 and Gint4.T, which specifically bind with U87MG cells and with PDGFRβ, were linked with tFNA, to form Gint4.T-tFNA-GMT8 (GTG). GTG was efficiently internalized by U87MG and bEnd.3 cells and penetrated an in-vitro blood-brain-barrier model. GTG loaded with paclitaxel (GPC) had potentiated anti-glioma efficacy. It inhibited the proliferation, migration, and invasion of U87MG cells, and enhanced apoptosis induction in these cells. The expression of apoptosis-related proteins was significantly changed after treatment with GPC, confirming apoptosis induction. Our study demonstrated that the combination of GTG and paclitaxel has great potential for glioma treatment and tFNA shows great promise for use in drug delivery.
靶向 DNA 纳米颗粒已被确定为抗神经胶质瘤药物递送中最有前途的纳米载体之一。我们建立了一种用于靶向神经胶质瘤治疗的多功能纳米系统。选择进入 U87MG 细胞和 bEnd.3 细胞的四面体框架核酸 (tFNA) 来递送两种适体 GMT8 和 Gint4.T 以及紫杉醇。GMT8 和 Gint4.T 特异性结合 U87MG 细胞和 PDGFRβ,与 tFNA 连接,形成 Gint4.T-tFNA-GMT8 (GTG)。GTG 被 U87MG 和 bEnd.3 细胞有效内化,并穿透体外血脑屏障模型。负载紫杉醇的 GTG (GPC) 增强了抗神经胶质瘤功效。它抑制了 U87MG 细胞的增殖、迁移和侵袭,并增强了这些细胞的凋亡诱导。用 GPC 处理后,凋亡相关蛋白的表达明显改变,证实了凋亡诱导。我们的研究表明,GTG 和紫杉醇的联合具有很大的神经胶质瘤治疗潜力,tFNA 在药物递送中具有很大的应用潜力。