n/a
Abstract Title:

Cytotoxic effects of Garcinia mangostana pericarp extract in cancer cell lines.

Abstract Source:

Curr Drug Discov Technol. 2022 Jan 13. Epub 2022 Jan 13. PMID: 35049434

Abstract Author(s):

Roghayeh Rashidi, Fatemeh Forouzanfar, Mohammad Soukhtanloo, Shirin Ghasemian, Seyed Hadi Mousavi

Article Affiliation:

Roghayeh Rashidi

Abstract:

BACKGROUND: Garcinia mangostana, commonly also called mangosteen, is an evergreen tropical tree, and its pericarps have been used in traditional herbal medicine for different diseases. The anticancer efficacy of the ethanolic extract from pericarps of Garcinia mangostana was investigated in human prostate cancer cells (PC3), melanoma cells (B16F10), breast cancer cells (MCF7) and glioblastoma (U87) cell lines.

METHODS: 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay was used to measure cell viability. propidium iodide (PI) staining and analysis on a flow cytometer was used to identify apoptosis. Action on cell migration was evaluated by scratch assay and gelatin zymography. Furthermore, the level of intracellular reactive oxygen species (ROS), malondialdehyde (MDA), glutathione (GSH), and superoxide dismutase (SOD) activity was measured. Moreover, we investigated the synergistic efficacy with several combinations of Garcinia mangostana extract (GME) with doxorubicin.

RESULTS: GME reduced cell viability in malignant cell dose and time-dependently. GME-induced sub-G1 peak in flow cytometry histogram of treated cells control representing apoptotic cell death is involved in GME toxicity. Furthermore, GME exhibited inhibitory effects on the migration ability of U87 cells, which was accompanied by inhibition in the activity and expression of MMP2 (matrix metalloproteinase-2). Besides, GSH level and SOD activity was significantly reduced while there was an increase in ROS and MDA concentration following 24 hr GME treatment. Moreover, combination of GME (1.5-25μg/mL) with Dox (6 µg/mL) displayed synergistic efficacy and cell growth inhibition.

CONCLUSION: In conclusion, GME could cause cell death in PC3, MCF7, U87, and B16F10 cell lines, in which apoptosis plays an imperative role. Plant extract decreased the migration ability of the cells by inhibiting the activity and expression of Matrix metalloproteinases (MMPs). G. mangostana could be a promising therapeutic strategy to treat cancer in the future.

Study Type : In Vitro Study

Print Options


Key Research Topics

This website is for information purposes only. By providing the information contained herein we are not diagnosing, treating, curing, mitigating, or preventing any type of disease or medical condition. Before beginning any type of natural, integrative or conventional treatment regimen, it is advisable to seek the advice of a licensed healthcare professional.

© Copyright 2008-2024 GreenMedInfo.com, Journal Articles copyright of original owners, MeSH copyright NLM.