Inhibition of Growth and Induction of Apoptosis in Fibrosarcoma Cell Lines by Echinophora platyloba DC: In Vitro Analysis

Echinophora platyloba DC plant (Khousharizeh) is one of the indigenous medicinal plants which is used as a food seasoning and medicine in Iran. The objective of this study was to examine the in vitro cytotoxic activity and the mechanism of cell death of crude methanolic extracts prepared from Echino...

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Main Authors: Fatemeh Zare Shahneh, Samira Valiyari, Abbas Azadmehr, Reza Hajiaghaee, Saeid Yaripour, Ali Bandehagh, Behzad Baradaran
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Advances in Pharmacological Sciences
Online Access:http://dx.doi.org/10.1155/2013/512931
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author Fatemeh Zare Shahneh
Samira Valiyari
Abbas Azadmehr
Reza Hajiaghaee
Saeid Yaripour
Ali Bandehagh
Behzad Baradaran
author_facet Fatemeh Zare Shahneh
Samira Valiyari
Abbas Azadmehr
Reza Hajiaghaee
Saeid Yaripour
Ali Bandehagh
Behzad Baradaran
author_sort Fatemeh Zare Shahneh
collection DOAJ
description Echinophora platyloba DC plant (Khousharizeh) is one of the indigenous medicinal plants which is used as a food seasoning and medicine in Iran. The objective of this study was to examine the in vitro cytotoxic activity and the mechanism of cell death of crude methanolic extracts prepared from Echinophora platyloba DC, on mouse fibrosarcoma cell line (WEHI-164). Cytotoxicity and viability of methanolic extract was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and dye exclusion assay. Cell death ELISA was employed to quantify the nucleosome production result from nuclear DNA fragmentation during apoptosis and determine whether the mechanism involves induction of apoptosis or necrosis. The cell death was identified as apoptosis using terminal deoxynucleotidyl transferase- (TdT-) mediated dUTP nick end labeling (TUNEL) assay. Our results demonstrated that the extract decreased cell viability, suppressed cell proliferation, and induced cell death in a time- and dose-dependent manner in WEHI-164 cells (IC50 = 196.673 ± 12.4 μg/mL) when compared with a chemotherapeutic anticancer drug, Toxol. Observation proved that apoptosis was the major mechanism of cell death. So the Echinophora platyloba DC extract was found to time- and dose-dependently inhibit the proliferation of fibrosarcoma cell possibly via an apoptosis-dependent pathway.
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spelling doaj-art-97a31a6dc664486ab2dfab4ad4c83e732025-02-03T01:27:30ZengWileyAdvances in Pharmacological Sciences1687-63341687-63422013-01-01201310.1155/2013/512931512931Inhibition of Growth and Induction of Apoptosis in Fibrosarcoma Cell Lines by Echinophora platyloba DC: In Vitro AnalysisFatemeh Zare Shahneh0Samira Valiyari1Abbas Azadmehr2Reza Hajiaghaee3Saeid Yaripour4Ali Bandehagh5Behzad Baradaran6Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, IranDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, IranDepartment of Immunology, Qazvin University of Medical Sciences, Qazvin, IranPharmacognosy and Pharmaceutics, Department of Medicinal Plants Research Center, Institute of Medicinal Plants, ACECR, Karaj, IranDepartment of Food and Drug Control, School of Pharmacy, Tehran University of Medical Science, Tehran, IranPlant Breeding and Biotechnology Department, Faculty of Agriculture, University of Tabriz, Tabriz, IranDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, IranEchinophora platyloba DC plant (Khousharizeh) is one of the indigenous medicinal plants which is used as a food seasoning and medicine in Iran. The objective of this study was to examine the in vitro cytotoxic activity and the mechanism of cell death of crude methanolic extracts prepared from Echinophora platyloba DC, on mouse fibrosarcoma cell line (WEHI-164). Cytotoxicity and viability of methanolic extract was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and dye exclusion assay. Cell death ELISA was employed to quantify the nucleosome production result from nuclear DNA fragmentation during apoptosis and determine whether the mechanism involves induction of apoptosis or necrosis. The cell death was identified as apoptosis using terminal deoxynucleotidyl transferase- (TdT-) mediated dUTP nick end labeling (TUNEL) assay. Our results demonstrated that the extract decreased cell viability, suppressed cell proliferation, and induced cell death in a time- and dose-dependent manner in WEHI-164 cells (IC50 = 196.673 ± 12.4 μg/mL) when compared with a chemotherapeutic anticancer drug, Toxol. Observation proved that apoptosis was the major mechanism of cell death. So the Echinophora platyloba DC extract was found to time- and dose-dependently inhibit the proliferation of fibrosarcoma cell possibly via an apoptosis-dependent pathway.http://dx.doi.org/10.1155/2013/512931
spellingShingle Fatemeh Zare Shahneh
Samira Valiyari
Abbas Azadmehr
Reza Hajiaghaee
Saeid Yaripour
Ali Bandehagh
Behzad Baradaran
Inhibition of Growth and Induction of Apoptosis in Fibrosarcoma Cell Lines by Echinophora platyloba DC: In Vitro Analysis
Advances in Pharmacological Sciences
title Inhibition of Growth and Induction of Apoptosis in Fibrosarcoma Cell Lines by Echinophora platyloba DC: In Vitro Analysis
title_full Inhibition of Growth and Induction of Apoptosis in Fibrosarcoma Cell Lines by Echinophora platyloba DC: In Vitro Analysis
title_fullStr Inhibition of Growth and Induction of Apoptosis in Fibrosarcoma Cell Lines by Echinophora platyloba DC: In Vitro Analysis
title_full_unstemmed Inhibition of Growth and Induction of Apoptosis in Fibrosarcoma Cell Lines by Echinophora platyloba DC: In Vitro Analysis
title_short Inhibition of Growth and Induction of Apoptosis in Fibrosarcoma Cell Lines by Echinophora platyloba DC: In Vitro Analysis
title_sort inhibition of growth and induction of apoptosis in fibrosarcoma cell lines by echinophora platyloba dc in vitro analysis
url http://dx.doi.org/10.1155/2013/512931
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