黑色素瘤
小RNA
微泡
免疫系统
细胞毒性
癌症研究
生物
细胞外小泡
转染
活力测定
细胞生长
细胞
细胞培养
分子生物学
体外
化学
细胞生物学
免疫学
生物化学
基因
遗传学
作者
Najla Adel Saleh,Michele Patrícia Rode,Júlia Cisilotto,Adny Henrique Silva,Anne Natalie Prigol,Fernanda da Luz Efe,Evelyn Winter,Fabíola Branco Filippin-Monteiro,Tânia Beatriz Creczynski‐Pasa
标识
DOI:10.1080/08820139.2023.2278774
摘要
Introduction Research in tumor treatment has shown promising results using extracellular vesicles (EVs) derived from immune cells. EVs derived from M1 macrophages (proinflammatory), known as M1-EVs, have properties that suppress tumor growth, making them a promising treatment tool for immune susceptible tumors such as melanoma. Here, small unaltered M1-EVs (M1-sEVs) were employed in a 3D mouse melanoma model (melanospheres) to evaluate such activity.
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