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Metformin enhances anti-cancer effects of cisplatin in meningioma through AMPK-mTOR signaling pathways
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 reporte...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851485/ https://www.ncbi.nlm.nih.gov/pubmed/33575476 http://dx.doi.org/10.1016/j.omto.2020.11.004 |
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author | Guo, Liemei Cui, Jing Wang, Herui Medina, Rogelio Zhang, Shilei Zhang, Xiaohua Zhuang, Zhengping Lin, Yingying |
author_facet | Guo, Liemei Cui, Jing Wang, Herui Medina, Rogelio Zhang, Shilei Zhang, Xiaohua Zhuang, Zhengping Lin, Yingying |
author_sort | Guo, Liemei |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7851485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-78514852021-02-10 Metformin enhances anti-cancer effects of cisplatin in meningioma through AMPK-mTOR signaling pathways Guo, Liemei Cui, Jing Wang, Herui Medina, Rogelio Zhang, Shilei Zhang, Xiaohua Zhuang, Zhengping Lin, Yingying Mol Ther Oncolytics Original Article 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. American Society of Gene & Cell Therapy 2020-11-20 /pmc/articles/PMC7851485/ /pubmed/33575476 http://dx.doi.org/10.1016/j.omto.2020.11.004 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Guo, Liemei Cui, Jing Wang, Herui Medina, Rogelio Zhang, Shilei Zhang, Xiaohua Zhuang, Zhengping Lin, Yingying Metformin enhances anti-cancer effects of cisplatin in meningioma through AMPK-mTOR signaling pathways |
title | Metformin enhances anti-cancer effects of cisplatin in meningioma through AMPK-mTOR signaling pathways |
title_full | Metformin enhances anti-cancer effects of cisplatin in meningioma through AMPK-mTOR signaling pathways |
title_fullStr | Metformin enhances anti-cancer effects of cisplatin in meningioma through AMPK-mTOR signaling pathways |
title_full_unstemmed | Metformin enhances anti-cancer effects of cisplatin in meningioma through AMPK-mTOR signaling pathways |
title_short | Metformin enhances anti-cancer effects of cisplatin in meningioma through AMPK-mTOR signaling pathways |
title_sort | metformin enhances anti-cancer effects of cisplatin in meningioma through ampk-mtor signaling pathways |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851485/ https://www.ncbi.nlm.nih.gov/pubmed/33575476 http://dx.doi.org/10.1016/j.omto.2020.11.004 |
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