阿霉素
雷公藤醇
抗药性
药品
纳米晶
纳米技术
抗癌药
药理学
生物相容性材料
化疗
材料科学
癌症研究
化学
医学
生物医学工程
内科学
生物化学
生物
细胞凋亡
微生物学
作者
Yating Xiao,Jing Liu,Mengyu Guo,Huige Zhou,Jun‐O Jin,Jiaming Liu,Ying Liu,Zhanjun Zhang,Chunying Chen
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2018-01-01
卷期号:10 (26): 12639-12649
被引量:97
摘要
A key challenge of chemotherapy in clinical treatments is multidrug resistance (MDR), which mainly arises from drug efflux-induced tumor cell survival. Thus, it is necessary to provide biocompatible chemotherapeutics to improve drug accumulation in MDR cells. Herein, two clinical small molecular drugs, celastrol (CST) and doxorubicin (DOX), were self-assembled into carrier-free and biocompatible nanoparticles (CST/DOX NPs) via a simple and green precipitation method for synergistic combination chemotherapy to overcome DOX resistance. These spherical CST/DOX NPs can improve the water-solubility of CST, reduce the dosage of DOX, and therefore significantly enhance cellular drug accumulation by activating heat shock factor 1 (HSF-1) and inhibiting NF-κB to depress P-gp expression, which results in apoptosis and autophagy of DOX resistant cells through the ROS/JNK signaling pathway. Finally, synergistic combination chemotherapy was attained in both MCF-7/MDR cells and 3D multicellular tumor spheroids. Thus, CST/DOX NPs provide an alternative for overcoming drug resistance in future clinical applications.
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