转铁蛋白
流式细胞术
癌症研究
干细胞
小RNA
转铁蛋白受体
细胞培养
化学
U87型
胶质母细胞瘤
分子生物学
生物
细胞生物学
生物化学
基因
遗传学
作者
Xinmei Wang,Xiaomeng Huang,Zhaogang Yang,Daniel Gallego‐Perez,Jun‐Yu Ma,Xi Zhao,Jing Xie,Ichiro Nakano,Li‐Na Lee
标识
DOI:10.2174/1389201015666141031105234
摘要
Tf-NPmiR- 1 treatment resulted in an over 200-fold increase of mature miR-1 compared to free miR-1 and Tf-NP-miR negative control (Tf-NP-miR-NC). Transferrin-mediated NP delivery resulted in a 3-fold higher delivery efficiency compared to NP without transferrin modification. Tf-NP-miR-1 treatment on GBM spheres significantly inhibited migration of GBM spheres by 30-50% with associated decline of MET and EGFR expression. Our data supported that Tf-NP could be used as an efficient and effective delivery system which has high potential to benefit the development of miR-based therapeutics for GBM treatment.
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