Mechanisms involved in the anti-tumor effects of Toosendanin in glioma cells

Abstract Background Toosendanin (TSN) is a triterpenoid compound mainly used as an ascaris repellant. Recent studies have shown that it possesses antitumor effects in many types of tumor cells. However, the effects of TSN on glioma cells have rarely been reported. Methods Different assays were perfo...

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Main Authors: Chaochao Zhang, Haijun Gao, Ziqiang Liu, Jiacheng Lai, Zhixin Zhan, Yong Chen, Haiyan Huang
Format: Article
Language:English
Published: BMC 2021-09-01
Series:Cancer Cell International
Subjects:
Online Access:https://doi.org/10.1186/s12935-021-02186-2
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author Chaochao Zhang
Haijun Gao
Ziqiang Liu
Jiacheng Lai
Zhixin Zhan
Yong Chen
Haiyan Huang
author_facet Chaochao Zhang
Haijun Gao
Ziqiang Liu
Jiacheng Lai
Zhixin Zhan
Yong Chen
Haiyan Huang
author_sort Chaochao Zhang
collection DOAJ
description Abstract Background Toosendanin (TSN) is a triterpenoid compound mainly used as an ascaris repellant. Recent studies have shown that it possesses antitumor effects in many types of tumor cells. However, the effects of TSN on glioma cells have rarely been reported. Methods Different assays were performed to investigate the effects of TSN on the different glioma cell lines including U87MG and LN18. The assays included colony formation, wound healing, and transwell assays. Furthermore, Hoechst 33342 staining, flow cytometry, and western blotting analysis were performed to investigate the apoptotic activities of TSN. Finally, the results were confirmed using a xenograft tumor model that comprised of nude mice. Results In vitro, the CCK-8 and colony formation assays showed that TSN effectively inhibited glioma cell proliferation. Moreover, the inhibitory effects on glioma cell migration and invasion were demonstrated through the wound healing and transwell assays, respectively. Hoechst 33342 staining, flow cytometry, and western blotting assays demonstrated the significant effect of TSN in the apoptosis induction of glioma cells. Furthermore, the anti-glioma effect of TSN was exerted through the inhibition of the PI3K/Akt/mTOR signaling pathways as demonstrated by western blotting analysis. In addition, the effects of TSN on glioma cell viability, apoptosis, cell cycle arrest, migration, and invasion were reversed by 740Y-P, a PI3K activator. Finally, the mouse xenograft model confirmed the suppressive effect of TSN on tumor growth in vivo. Conclusion Our results suggest that TSN is a promising chemotherapeutic drug for patients with glioma.
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spelling doaj.art-61c95ef16c054dd49d35b87323fd63e22022-12-21T21:35:50ZengBMCCancer Cell International1475-28672021-09-0121111310.1186/s12935-021-02186-2Mechanisms involved in the anti-tumor effects of Toosendanin in glioma cellsChaochao Zhang0Haijun Gao1Ziqiang Liu2Jiacheng Lai3Zhixin Zhan4Yong Chen5Haiyan Huang6Department of Neurosurgery, The First Hospital of Jilin UniversityDepartment of Neurosurgery, The First Hospital of Jilin UniversityDepartment of Neurosurgery, The First Hospital of Jilin UniversityDepartment of Neurosurgery, The First Hospital of Jilin UniversityDepartment of Neurosurgery, The First Hospital of Jilin UniversityDepartment of Neurosurgery, The First Hospital of Jilin UniversityDepartment of Neurosurgery, The First Hospital of Jilin UniversityAbstract Background Toosendanin (TSN) is a triterpenoid compound mainly used as an ascaris repellant. Recent studies have shown that it possesses antitumor effects in many types of tumor cells. However, the effects of TSN on glioma cells have rarely been reported. Methods Different assays were performed to investigate the effects of TSN on the different glioma cell lines including U87MG and LN18. The assays included colony formation, wound healing, and transwell assays. Furthermore, Hoechst 33342 staining, flow cytometry, and western blotting analysis were performed to investigate the apoptotic activities of TSN. Finally, the results were confirmed using a xenograft tumor model that comprised of nude mice. Results In vitro, the CCK-8 and colony formation assays showed that TSN effectively inhibited glioma cell proliferation. Moreover, the inhibitory effects on glioma cell migration and invasion were demonstrated through the wound healing and transwell assays, respectively. Hoechst 33342 staining, flow cytometry, and western blotting assays demonstrated the significant effect of TSN in the apoptosis induction of glioma cells. Furthermore, the anti-glioma effect of TSN was exerted through the inhibition of the PI3K/Akt/mTOR signaling pathways as demonstrated by western blotting analysis. In addition, the effects of TSN on glioma cell viability, apoptosis, cell cycle arrest, migration, and invasion were reversed by 740Y-P, a PI3K activator. Finally, the mouse xenograft model confirmed the suppressive effect of TSN on tumor growth in vivo. Conclusion Our results suggest that TSN is a promising chemotherapeutic drug for patients with glioma.https://doi.org/10.1186/s12935-021-02186-2ToosendaninGliomaApoptosisProliferationPI3KAkt
spellingShingle Chaochao Zhang
Haijun Gao
Ziqiang Liu
Jiacheng Lai
Zhixin Zhan
Yong Chen
Haiyan Huang
Mechanisms involved in the anti-tumor effects of Toosendanin in glioma cells
Cancer Cell International
Toosendanin
Glioma
Apoptosis
Proliferation
PI3K
Akt
title Mechanisms involved in the anti-tumor effects of Toosendanin in glioma cells
title_full Mechanisms involved in the anti-tumor effects of Toosendanin in glioma cells
title_fullStr Mechanisms involved in the anti-tumor effects of Toosendanin in glioma cells
title_full_unstemmed Mechanisms involved in the anti-tumor effects of Toosendanin in glioma cells
title_short Mechanisms involved in the anti-tumor effects of Toosendanin in glioma cells
title_sort mechanisms involved in the anti tumor effects of toosendanin in glioma cells
topic Toosendanin
Glioma
Apoptosis
Proliferation
PI3K
Akt
url https://doi.org/10.1186/s12935-021-02186-2
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AT jiachenglai mechanismsinvolvedintheantitumoreffectsoftoosendaniningliomacells
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