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二甲双胍通过AMPK-mTOR信号通路增强顺铂对脑膜瘤的抗癌作用。

Metformin enhances anti-cancer effects of cisplatin in meningioma through AMPK-mTOR signaling pathways.

作者信息

Guo Liemei, Cui Jing, Wang Herui, Medina Rogelio, Zhang Shilei, Zhang Xiaohua, Zhuang Zhengping, Lin Yingying

机构信息

Department of Neurosurgery, Renji Hospital, School of Medicine, Shanghai Jiaotong University, No. 160, Pujian Road, District Pudong, Shanghai 200127, China.

Neuro-Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Mol Ther Oncolytics. 2020 Nov 20;20:119-131. doi: 10.1016/j.omto.2020.11.004. eCollection 2021 Mar 26.

Abstract

Cisplatin is currently used to treat inoperable recurrent meningiomas, but its side effects and drug resistance limit its use. Metformin has recently been identified as a chemosensitizing agent. However, the combined treatment of cisplatin and metformin in high-grade meningiomas has not been reported. Herein, our findings demonstrate metformin significantly enhanced cisplatin-induced inhibition of proliferation in meningioma cells, which was associated with the induction of G0/G1 cell cycle arrest. Additionally, metformin activated adenosine monophosphate activated protein kinase (AMPK) and repressed the mammalian target of rapamycin (mTOR) signaling pathways via an AMPK-dependent mechanism. Furthermore, our xenograft murine model confirmed that metformin enhanced cisplatin's anti-cancer effect by upregulation of AMPK and downregulation of mTOR signaling pathways. In addition, in 63 patients with atypical meningiomas, the activation of AMPK was significantly associated with tumor recurrence and short disease-free survival (DFS). These results demonstrate metformin enhanced the anti-cancer effect of cisplatin in meningioma and , an effect mediated through the activation of AMPK and repression of mTOR signaling pathways. Our study suggests the combined treatment of metformin and cisplatin is an effective and safe treatment for high-grade meningiomas.

摘要

顺铂目前用于治疗无法手术的复发性脑膜瘤,但其副作用和耐药性限制了其应用。二甲双胍最近被确定为一种化学增敏剂。然而,顺铂和二甲双胍联合治疗高级别脑膜瘤的情况尚未见报道。在此,我们的研究结果表明,二甲双胍显著增强了顺铂诱导的脑膜瘤细胞增殖抑制作用,这与诱导G0/G1细胞周期停滞有关。此外,二甲双胍激活了腺苷单磷酸激活蛋白激酶(AMPK),并通过一种依赖AMPK的机制抑制了雷帕霉素靶蛋白(mTOR)信号通路。此外,我们的异种移植小鼠模型证实,二甲双胍通过上调AMPK和下调mTOR信号通路增强了顺铂的抗癌作用。此外,在63例非典型脑膜瘤患者中,AMPK的激活与肿瘤复发和无病生存期(DFS)短显著相关。这些结果表明,二甲双胍增强了顺铂在脑膜瘤中的抗癌作用,这种作用是通过激活AMPK和抑制mTOR信号通路介导的。我们的研究表明,二甲双胍和顺铂联合治疗是高级别脑膜瘤一种有效且安全的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8166/7851485/d21587b1385e/fx1.jpg

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