自噬
ATG5型
癌细胞
细胞生物学
程序性细胞死亡
沃特曼宁
生物
自噬体
胞饮病
细胞
PI3K/AKT/mTOR通路
化学
细胞凋亡
信号转导
生物化学
癌症
内吞作用
遗传学
作者
Jun Lin,Zhihai Huang,Hao Wu,Wei Zhou,Peipei Jin,Pengfei Wei,Yunjiao Zhang,Fang Zheng,Jiqian Zhang,Jing Xu,Yi Hu,Yanhong Wang,Yajuan Li,Ning Gu,Longping Wen
出处
期刊:Autophagy
[Taylor & Francis]
日期:2014-11-02
卷期号:10 (11): 2006-2020
被引量:218
摘要
Silver nanoparticles (Ag NPs) are cytotoxic to cancer cells and possess excellent potential as an antitumor agent. A variety of nanoparticles have been shown to induce autophagy, a critical cellular degradation process, and the elevated autophagy in most of these situations promotes cell death. Whether Ag NPs can induce autophagy and how it might affect the anticancer activity of Ag NPs has not been reported. Here we show that Ag NPs induced autophagy in cancer cells by activating the PtdIns3K signaling pathway. The autophagy induced by Ag NPs was characterized by enhanced autophagosome formation, normal cargo degradation, and no disruption of lysosomal function. Consistent with these properties, the autophagy induced by Ag NPs promoted cell survival, as inhibition of autophagy by either chemical inhibitors or ATG5 siRNA enhanced Ag NPs-elicited cancer cell killing. We further demonstrated that wortmannin, a widely used inhibitor of autophagy, significantly enhanced the antitumor effect of Ag NPs in the B16 mouse melanoma cell model. Our results revealed a novel biological activity of Ag NPs in inducing cytoprotective autophagy, and inhibition of autophagy may be a useful strategy for improving the efficacy of Ag NPs in anticancer therapy.
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