纳米载体
三阴性乳腺癌
细胞凋亡
癌症研究
药物输送
PI3K/AKT/mTOR通路
癌细胞
细胞毒性
化学
药理学
阿霉素
靶向给药
红细胞
体内
癌症
乳腺癌
化疗
生物
医学
体外
生物化学
内科学
生物技术
有机化学
作者
Chenxi Li,Jiaxin Zhang,Xianxian Yao,Yuxin Huang,Yingze Zhang,Wuli Yang
标识
DOI:10.1088/1748-605x/add4da
摘要
Abstract The application of the conventional drugs for triple-negative breast cancer (TNBC) treatment in chemotherapy is limited due to their intrinsic drawbacks such as short drug half-life, lack of tumor selectivity and systemic toxicity. Herein, an effective nanoparticle drug delivery system (NDDS) of red blood cell (RBC) membrane-camouflaged piperlongumine (PL)-loaded iron oxide (Fe 3 O 4 ) magnetic nanoparticles (Fe 3 O 4 -PL@RBC) was rationally designed as an effective drug delivery platform for in vivo TNBC treatment. The Fe 3 O 4 -PL@RBC showed considerable cytotoxicity against MDA-MB-231 cells, inducing intracellular accumulation of reactive oxygen species, mitochondrial dysfunction and apoptosis. Furthermore, transcriptomic analyses and western blotting analysis demonstrated that the Fe 3 O 4 -PL@RBC induced apoptosis through the inhibition of PI3K/AKT/mTOR pathway and downregulation of Bcl-2 protein. In MDA-MB-231 tumor models, the RBC membrane coating in Fe 3 O 4 -PL@RBC effectively prolonged the circulation time and sufficient enrichment at the tumor sites. And the Fe 3 O 4 -PL@RBC significantly inhibited tumor growth with good biosafety. This study provides guidance for the rational design of effective Fe 3 O 4 -based NDDS for TNBC treatment.
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