Silver Nanotriangles and Chemotherapeutics Synergistically Induce Apoptosis in Glioma Cells via a ROS-Dependent Mitochondrial Pathway

Silver Nanotriangles and Chemotherapeutics Synergistically Induce Apoptosis in Glioma Cells via a ROS-Dependent Mitochondrial Pathway
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DOI:
10.2147/ijn.s267120
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发表时间:
2020
影响因子:
8
通讯作者:
Jing Zhao
Jing Zhao
中科院分区:
医学2区
文献类型:
--
作者:
Huiquan Yang;Wenbin Chen;Jun Ma;Jing Zhao

文献摘要

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Background: The synergistic effect of nanomaterials and chemotherapeutics provides.a novel strategy for the treatment of tumors. Silver nanotriangles (AgNTs) exhibited some.unique properties in nanomedicine. Studies on the synergy of silver-based nanomaterials and.anti-tumor drugs against gliomas are rare..Materials and Methods: Chitosan-coated AgNTs were prepared, followed by character-.ization using transmission electron microscopy, ultraviolet-visible spectroscopy and X-ray.diffraction. The anti-glioma effect of cyclophosphamide (CTX), 5-fluorouracil (5-FU), oxa-.liplatin (OXA), doxorubicin (DOX) or gemcitabine (GEM) combined with AgNTs in differ-.ent glioma cell lines (U87, U251 and C6) was assessed by the MTT assay to screen out.a drug with the most broad-spectrum and strongest synergistic anti-glioma activity. The.intracellular reactive oxygen species (ROS) level, mitochondrial membrane potential (MMP).and cell apoptosis were detected by flow cytometry. The possible underlying mechanisms of.the synergy were further investigated with ROS scavenger and specific inhibitors of C-jun.N-terminal kinase (JNK), p38 and extracellular signal-regulated kinase 1/2 pathways..Results: The synthesized AgNTs were mainly triangular and truncated triangular with an.average edge length of 125 nm. A synergistic anti-glioma effect of AgNTs combined with.CTX was not observed, and the synergism between AgNTs and 5-FU was cell type-specific..AgNTs combined with OXA, DOX or GEM displayed synergistic effects in various glioma.cell lines, and the combination of AgNTs and GEM showed the strongest synergistic activity..A decrease in cell viability, loss of the MMP and an increase in apoptosis rate induced by this.synergy could be significantly attenuated by the ROS scavenger N-acetylcysteine and JNK.inhibitor SP600125..Conclusion: Our results suggested that the combination of AgNTs and GEM possessed.broad-spectrum and potent synergistic anti-glioma activity, resulting from cell apoptosis.mediated by a ROS-dependent mitochondrial pathway in which JNK might be involved.