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自噬抑制增强了LY3023414诱导的抗胶质瘤细胞活性 以及 。(原文结尾不完整)

Autophagy inhibition sensitizes LY3023414-induced anti-glioma cell activity and .

作者信息

Zheng Lan, Li Huanyin, Mo Yanqing, Qi Gong, Liu Bin, Zhao Jing

机构信息

Neurology Department, Minhang Hospital, Fudan University, Shanghai, China.

出版信息

Oncotarget. 2017 Oct 27;8(58):98964-98973. doi: 10.18632/oncotarget.22147. eCollection 2017 Nov 17.

Abstract

PI3K-AKT-mTOR signaling is a valuable treatment target for human glioma. LY3023414 is a novel, highly-potent and pan PI3K-AKT-mTOR inhibitor. Here, we show that LY3023414 efficiently inhibited survival and proliferation of primary and established human glioma cells. Meanwhile, apoptosis activation was observed in LY3023414-treated glioma cells. LY3023414 blocked AKT-mTOR activation in human glioma cells. Further studies show that LY3023414 induced feedback activation of autophagy in U251MG cells. On the other hand, autophagy inhibition via adding pharmacological inhibitors or silencing Beclin-1/ATG-5 significantly potentiated LY3023414-induced glioma cell apoptosis. studies demonstrated that U251MG xenograft tumor growth in mice was suppressed by oral administration of LY3023414. Remarkably, LY3023414's anti-tumor activity was further augmented against the Beclin-1-silenced U251MG tumors. Together, our results suggest that targeting PI3K-AKT-mTOR cascade by LY3023414 inhibits human glioma cell growth and . Autophagy inhibition could further sensitize LY3023414 against human glioma cells.

摘要

PI3K-AKT-mTOR信号通路是人类胶质瘤的一个有价值的治疗靶点。LY3023414是一种新型、高效的泛PI3K-AKT-mTOR抑制剂。在此,我们表明LY3023414能有效抑制原代和已建立的人类胶质瘤细胞的存活和增殖。同时,在LY3023414处理的胶质瘤细胞中观察到凋亡激活。LY3023414阻断了人类胶质瘤细胞中的AKT-mTOR激活。进一步研究表明,LY3023414在U251MG细胞中诱导自噬的反馈激活。另一方面,通过添加药理抑制剂或沉默Beclin-1/ATG-5来抑制自噬,可显著增强LY3023414诱导的胶质瘤细胞凋亡。研究表明,口服LY3023414可抑制小鼠体内U251MG异种移植瘤的生长。值得注意的是,LY3023414对Beclin-1沉默的U251MG肿瘤的抗肿瘤活性进一步增强。总之,我们的结果表明,LY3023414靶向PI3K-AKT-mTOR级联可抑制人类胶质瘤细胞生长,并且自噬抑制可进一步使LY3023414对人类胶质瘤细胞敏感。

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