RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The Potential of Magnetic Targeted Natural Killer Cell Therapy for Glioblastoma: An in Vivo Study of Natural Killer Cells Loaded With Low-Temperature Synthesized Folic Acid-Modified Superparamagnetic Iron Oxide Nanoparticles.
The Potential of Magnetic Targeted Natural Killer Cell Therapy for Glioblastoma: An in Vivo Study of Natural Killer Cells Loaded With Low-Temperature Synthesized Folic Acid-Modified Superparamagnetic Iron Oxide Nanoparticles.
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负载 SPIONs-PEG-FA 的 NK 细胞是靶向 GBM 治疗的一种有前景的方法。
胶质母细胞瘤(GBM)是一种高度恶性的脑肿瘤,治疗选择有限。自然杀伤(NK)细胞免疫疗法虽在癌症治疗中显示出前景,但有效靶向肿瘤仍是挑战。本研究探讨使用叶酸修饰的超顺磁性氧化铁纳米颗粒(SPIONs-PEG-FA)使NK细胞磁化,以便在外部磁场作用下富集于肿瘤部位,同时保留其对GBM细胞的细胞毒活性。
采用PEG化和共沉淀法合成SPIONs-PEG-FA,确保NK细胞高效摄取。通过X射线衍射、傅里叶变换红外光谱、透射电子显微镜和动态光散射等材料表征方法确认成功合成。体外研究评估其安全性、细胞摄取和细胞溶解活性;体内实验则在GBM荷瘤小鼠中评估肿瘤靶向性和治疗效果。
成功制备了负载SPIONs-PEG-FA的NK细胞,用于靶向治疗GBM。体外研究证实其安全性以及对GBM肿瘤细胞的杀伤效果;透射电子显微镜分析确认NK细胞摄取了SPIONs-PEG-FA。在GBM荷瘤小鼠中进行的体内实验显示,SPIONs-PEG-FA负载NK细胞具有更好的肿瘤靶向性、更强的细胞溶解效率,且总体安全性良好。
SPIONs-PEG-FA负载NK细胞是治疗GBM的一种有前景的方法。其成功制备和表征,以及体内外验证结果,凸显了改善治疗结局的潜力。这种磁场引导的NK细胞疗法为克服GBM治疗挑战提供了有前景的策略。
SPIONs-PEG-FA were synthesized using PEGylation and coprecipitation to ensure efficient NK cell uptake. Their successful synthesis was confirmed through material characterization, including X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and dynamic light scattering. In vitro studies evaluated their safety, cellular uptake, and cytolytic activity, whereas in vivo experiments assessed tumor targeting and therapeutic efficacy in GBM-bearing mice.
SPIONs-PEG-FA-loaded NK cells were successfully developed for targeted GBM therapy. In vitro studies confirmed their safety and effectiveness against GBM tumor cells, whereas transmission electron microscopy analysis verified the cellular uptake of SPIONs-PEG-FA by NK cells. In vivo experiments in GBM-bearing mice demonstrated improved tumor targeting, enhanced cytolytic efficiency, and overall safety of SPIONs-PEG-FA-loaded NK cells.
SPIONs-PEG-FA-loaded NK cells represent a promising approach for targeted GBM therapy. Their successful synthesis and characterization, coupled with in vitro and in vivo validation, highlight their potential for improved therapeutic outcomes. This magnetic field-guided NK cell therapy offers a promising strategy for overcoming challenges in GBM treatment.
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