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

Authors :
Xiaohua Zhang
Liemei Guo
Jing Cui
Zhengping Zhuang
Yingying Lin
Herui Wang
Rogelio Medina
Shilei Zhang
Source :
Molecular Therapy Oncolytics, Molecular Therapy: Oncolytics, Vol 20, Iss, Pp 119-131 (2021)
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

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 in vitro and in vivo, 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.<br />Graphical Abstract<br />Lin, Zhuang, and their scholars confirmed for the first time that metformin combined with cisplatin is a safe and effective treatment for high-grade meningioma. This study illuminates a new direction for treating high-grade meningioma.

Details

ISSN :
23727705
Volume :
20
Database :
OpenAIRE
Journal :
Molecular Therapy - Oncolytics
Accession number :
edsair.doi.dedup.....2b475b8b9b54296caa3ea4a26c94c990