School of Medicine Publications and Presentations
Document Type
Article
Publication Date
4-3-2023
Abstract
Objectives
Glioblastoma multiforme (GBM) is a common and fatal brain tumour in the central nervous system with a poor survival rate and a median survival time of 15 months only. The standard treatment is aggressive surgical resection followed by radiotherapy and chemotherapy. However, effective drugs available in chemotherapy are limited. This study was designed to evaluate, for the first time, the potential therapeutic effect of Cissus quadrangularis (CQ) in human glioblastoma cells and to investigate its possible mechanisms of action. Methods
In this study, we examined the anticancer activity of CQ in human glioblastoma U87 MG cells by cell viability assay, cell migration assay, immunofluorescence staining and Western blot. Results
Our results demonstrated that CQ treatment induced U87 cytotoxicity, cell cycle arrest and cell death. The cytotoxicity of CQ mediates ER stress, autophagy and mitochondrial apoptosis by suppressing pro-survival signalling pathways (extracellular signal-regulated kinase and signal transducer and activator of transcription 3 pathways). Conclusions
The findings of this study imply that CQ is a promising anti-cancer candidate for the treatment of GBM. Highlights
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The anticancer effect of Cissus quadrangularis (CQ) was studied in human glioblastoma U87 MG cells.
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It was demonstrated that CQ treatment induced cytotoxicity, cell cycle arrest and cell death in U87 MG cells.
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CQ may become a potential chemotherapy component for the treatment of glioblastoma multiforme.
Recommended Citation
Benxu Cheng and others, Anti-cancer effect of Cissus quadrangularis on human glioblastoma cells, RPS Pharmacy and Pharmacology Reports, Volume 2, Issue 2, April 2023, rqad014, https://doi.org/10.1093/rpsppr/rqad014
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
Publication Title
RPS Pharmacy and Pharmacology Reports
DOI
10.1093/rpsppr/rqad014
Academic Level
faculty
Mentor/PI Department
Molecular Science
Comments
© The Author(s) 2023