自噬
体内
自噬体
体外
免疫印迹
化学
溶酶体
癌症研究
细胞生物学
生物化学
生物
酶
细胞凋亡
基因
生物技术
作者
Yali Liu,Wuyi Liu,Jingbin� Huang,Wenjing Lai,Faning Leng,Changpeng� Hu,Qian Zhang,Min Zhou,Qin Tang,Fangfang Sheng,Guobing� Li,Rong Zhang
出处
期刊:Nanomedicine
[Future Medicine]
日期:2019-05-01
卷期号:14 (10): 1307-1321
被引量:5
标识
DOI:10.2217/nnm-2018-0284
摘要
Aim: To confirm Cu2-xSe nanoparticles (NPs) could inhibit autophagic degradation and based on this property to develop a novel therapeutic strategy for cancer treatment. Materials & methods: Transmission electronic microscopy and confocal laser-scanning microscope were used to observe the accumulation of autophagosome. Western blot was used to investigate the expression of autophagy-associated proteins. Chemotherapeutic drug oxaliplatin was cotreatment with Cu2-xSe in vivo and in vitro to study therapeutic efficacy of autophagy caused by Cu2-xSe NPs. Results & conclusion: Cu2-xSe NPs significantly induce autophagosome accumulation in hepatocellular carcinoma cells, and they mainly inhibit the late-stage autophagy degradation through reducing lysosomal cathepsin activity. Moreover, Cu2-xSe NPs enhance the anticancer activity of oxaliplatin in vivo and in vitro through blocking autophagosome degradation.
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