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Cu2-xSe nanoparticles enhance the anticancer activity of oxaliplatin by inhibiting autophagic degradation
by
Sheng, Fangfang
, Leng, Faning
, Lai, Wenjing
, Zhou, Min
, Liu, Yali
, Li, Guobing
, Hu, Changpeng
, Zhang, Qian
, Huang, Jingbin
, Zhang, Rong
, Liu, Wuyi
, Tang, Qin
in
Alzheimer's disease
/ Apoptosis
/ Autophagy
/ Cancer therapies
/ Chemotherapy
/ Drug resistance
/ Liver cancer
/ Metabolism
/ Microscopy
/ Nanocrystals
/ Nanomaterials
/ Nanoparticles
/ Quantum dots
2019
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Cu2-xSe nanoparticles enhance the anticancer activity of oxaliplatin by inhibiting autophagic degradation
by
Sheng, Fangfang
, Leng, Faning
, Lai, Wenjing
, Zhou, Min
, Liu, Yali
, Li, Guobing
, Hu, Changpeng
, Zhang, Qian
, Huang, Jingbin
, Zhang, Rong
, Liu, Wuyi
, Tang, Qin
in
Alzheimer's disease
/ Apoptosis
/ Autophagy
/ Cancer therapies
/ Chemotherapy
/ Drug resistance
/ Liver cancer
/ Metabolism
/ Microscopy
/ Nanocrystals
/ Nanomaterials
/ Nanoparticles
/ Quantum dots
2019
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Cu2-xSe nanoparticles enhance the anticancer activity of oxaliplatin by inhibiting autophagic degradation
by
Sheng, Fangfang
, Leng, Faning
, Lai, Wenjing
, Zhou, Min
, Liu, Yali
, Li, Guobing
, Hu, Changpeng
, Zhang, Qian
, Huang, Jingbin
, Zhang, Rong
, Liu, Wuyi
, Tang, Qin
in
Alzheimer's disease
/ Apoptosis
/ Autophagy
/ Cancer therapies
/ Chemotherapy
/ Drug resistance
/ Liver cancer
/ Metabolism
/ Microscopy
/ Nanocrystals
/ Nanomaterials
/ Nanoparticles
/ Quantum dots
2019
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Cu2-xSe nanoparticles enhance the anticancer activity of oxaliplatin by inhibiting autophagic degradation
Journal Article
Cu2-xSe nanoparticles enhance the anticancer activity of oxaliplatin by inhibiting autophagic degradation
2019
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Overview
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.
Publisher
Future Medicine Ltd
Subject
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