Antioxidant Activity and ROS-Dependent Apoptotic Effect of Scurrula ferruginea (Jack) Danser Methanol Extract in Human Breast Cancer Cell MDA-MB-231

Scurrula ferruginea (Jack) Danser is one of the mistletoe species belonging to Loranthaceae family, which grows on the branches of many deciduous trees in tropical countries. This study evaluated the antioxidant activities of S. ferruginea extracts. The cytotoxic activity of the selected extracts, w...

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Veröffentlicht in:PloS one 2016-07, Vol.11 (7), p.e0158942-e0158942
Hauptverfasser: Marvibaigi, Mohsen, Amini, Neda, Supriyanto, Eko, Abdul Majid, Fadzilah Adibah, Kumar Jaganathan, Saravana, Jamil, Shajarahtunnur, Hamzehalipour Almaki, Javad, Nasiri, Rozita
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container_start_page e0158942
container_title PloS one
container_volume 11
creator Marvibaigi, Mohsen
Amini, Neda
Supriyanto, Eko
Abdul Majid, Fadzilah Adibah
Kumar Jaganathan, Saravana
Jamil, Shajarahtunnur
Hamzehalipour Almaki, Javad
Nasiri, Rozita
description Scurrula ferruginea (Jack) Danser is one of the mistletoe species belonging to Loranthaceae family, which grows on the branches of many deciduous trees in tropical countries. This study evaluated the antioxidant activities of S. ferruginea extracts. The cytotoxic activity of the selected extracts, which showed potent antioxidant activities, and high phenolic and flavonoid contents, were investigated in human breast cancer cell line (MDA-MB-231) and non-cancer human skin fibroblast cells (HSF-1184). The activities and characteristics varied depending on the different parts of S. ferruginea, solvent polarity, and concentrations of extracts. The stem methanol extract showed the highest amount of both phenolic (273.51 ± 4.84 mg gallic acid/g extract) and flavonoid contents (163.41 ± 4.62 mg catechin/g extract) and strong DPPH• radical scavenging (IC50 = 27.81 μg/mL) and metal chelation activity (IC50 = 80.20 μg/mL). The stem aqueous extract showed the highest ABTS•+ scavenging ability. The stem methanol and aqueous extracts exhibited dose-dependent cytotoxic activity against MDA-MB-231 cells with IC50 of 19.27 and 50.35 μg/mL, respectively. Furthermore, the extracts inhibited the migration and colony formation of MDA-MB-231 cells in a concentration-dependent manner. Morphological observations revealed hallmark properties of apoptosis in treated cells. The methanol extract induced an increase in ROS generation and mitochondrial depolarization in MDA-MB-231 cells, suggesting its potent apoptotic activity. The present study demonstrated that the S. ferruginea methanol extract mediated MDA-MB-231 cell growth inhibition via induction of apoptosis which was confirmed by Western blot analysis. It may be a potential anticancer agent; however, its in vivo anticancer activity needs to be investigated.
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This study evaluated the antioxidant activities of S. ferruginea extracts. The cytotoxic activity of the selected extracts, which showed potent antioxidant activities, and high phenolic and flavonoid contents, were investigated in human breast cancer cell line (MDA-MB-231) and non-cancer human skin fibroblast cells (HSF-1184). The activities and characteristics varied depending on the different parts of S. ferruginea, solvent polarity, and concentrations of extracts. The stem methanol extract showed the highest amount of both phenolic (273.51 ± 4.84 mg gallic acid/g extract) and flavonoid contents (163.41 ± 4.62 mg catechin/g extract) and strong DPPH• radical scavenging (IC50 = 27.81 μg/mL) and metal chelation activity (IC50 = 80.20 μg/mL). The stem aqueous extract showed the highest ABTS•+ scavenging ability. The stem methanol and aqueous extracts exhibited dose-dependent cytotoxic activity against MDA-MB-231 cells with IC50 of 19.27 and 50.35 μg/mL, respectively. Furthermore, the extracts inhibited the migration and colony formation of MDA-MB-231 cells in a concentration-dependent manner. Morphological observations revealed hallmark properties of apoptosis in treated cells. The methanol extract induced an increase in ROS generation and mitochondrial depolarization in MDA-MB-231 cells, suggesting its potent apoptotic activity. The present study demonstrated that the S. ferruginea methanol extract mediated MDA-MB-231 cell growth inhibition via induction of apoptosis which was confirmed by Western blot analysis. It may be a potential anticancer agent; however, its in vivo anticancer activity needs to be investigated.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0158942</identifier><identifier>PMID: 27410459</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Anticancer properties ; Antioxidants ; Antioxidants (Nutrients) ; Antioxidants - chemistry ; Antioxidants - isolation &amp; purification ; Antioxidants - metabolism ; Antioxidants - pharmacology ; Antitumor activity ; Apoptosis ; Apoptosis - drug effects ; Biology and Life Sciences ; Biphenyl Compounds - metabolism ; Branches ; Breast cancer ; Breast Neoplasms - pathology ; Cancer ; Care and treatment ; Caspase 3 - metabolism ; Caspase 7 - metabolism ; Catechin ; Cell Line, Tumor ; Cell Movement - drug effects ; Cell Nucleus - drug effects ; Cell Proliferation - drug effects ; Chelation ; Cytotoxicity ; Deciduous trees ; Depolarization ; Drug therapy ; Flavonoids - analysis ; Gallic acid ; Humans ; In vivo methods and tests ; Iron - metabolism ; Loranthaceae ; Medicine and Health Sciences ; Membrane Potential, Mitochondrial - drug effects ; Methanol ; Methanol - chemistry ; Mistletoes ; Mitochondria ; Phenolic compounds ; Phenols ; Phenols - analysis ; Physical Sciences ; Picrates - metabolism ; Plant Extracts - chemistry ; Plant Extracts - isolation &amp; purification ; Plant Extracts - metabolism ; Plant Extracts - pharmacology ; Plant Stems - chemistry ; Polarity ; Poly(ADP-ribose) Polymerases - metabolism ; Reactive Oxygen Species - metabolism ; Research and Analysis Methods ; Risk factors ; Santalales ; Scavenging ; Skin ; Tracheophyta - chemistry ; Viscum album ; Water - chemistry</subject><ispartof>PloS one, 2016-07, Vol.11 (7), p.e0158942-e0158942</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Marvibaigi et al. 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Amini, Neda ; Supriyanto, Eko ; Abdul Majid, Fadzilah Adibah ; Kumar Jaganathan, Saravana ; Jamil, Shajarahtunnur ; Hamzehalipour Almaki, Javad ; Nasiri, Rozita</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c725t-8ceb2d40070820c155e2271f2b7730665828fd16269ec811fb2511e99f17575d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Anticancer properties</topic><topic>Antioxidants</topic><topic>Antioxidants (Nutrients)</topic><topic>Antioxidants - chemistry</topic><topic>Antioxidants - isolation &amp; purification</topic><topic>Antioxidants - metabolism</topic><topic>Antioxidants - pharmacology</topic><topic>Antitumor activity</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Biology and Life Sciences</topic><topic>Biphenyl Compounds - metabolism</topic><topic>Branches</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - pathology</topic><topic>Cancer</topic><topic>Care and treatment</topic><topic>Caspase 3 - metabolism</topic><topic>Caspase 7 - metabolism</topic><topic>Catechin</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement - drug effects</topic><topic>Cell Nucleus - drug effects</topic><topic>Cell Proliferation - drug effects</topic><topic>Chelation</topic><topic>Cytotoxicity</topic><topic>Deciduous trees</topic><topic>Depolarization</topic><topic>Drug therapy</topic><topic>Flavonoids - analysis</topic><topic>Gallic acid</topic><topic>Humans</topic><topic>In vivo methods and tests</topic><topic>Iron - metabolism</topic><topic>Loranthaceae</topic><topic>Medicine and Health Sciences</topic><topic>Membrane Potential, Mitochondrial - drug effects</topic><topic>Methanol</topic><topic>Methanol - chemistry</topic><topic>Mistletoes</topic><topic>Mitochondria</topic><topic>Phenolic compounds</topic><topic>Phenols</topic><topic>Phenols - analysis</topic><topic>Physical Sciences</topic><topic>Picrates - metabolism</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - isolation &amp; 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This study evaluated the antioxidant activities of S. ferruginea extracts. The cytotoxic activity of the selected extracts, which showed potent antioxidant activities, and high phenolic and flavonoid contents, were investigated in human breast cancer cell line (MDA-MB-231) and non-cancer human skin fibroblast cells (HSF-1184). The activities and characteristics varied depending on the different parts of S. ferruginea, solvent polarity, and concentrations of extracts. The stem methanol extract showed the highest amount of both phenolic (273.51 ± 4.84 mg gallic acid/g extract) and flavonoid contents (163.41 ± 4.62 mg catechin/g extract) and strong DPPH• radical scavenging (IC50 = 27.81 μg/mL) and metal chelation activity (IC50 = 80.20 μg/mL). The stem aqueous extract showed the highest ABTS•+ scavenging ability. The stem methanol and aqueous extracts exhibited dose-dependent cytotoxic activity against MDA-MB-231 cells with IC50 of 19.27 and 50.35 μg/mL, respectively. Furthermore, the extracts inhibited the migration and colony formation of MDA-MB-231 cells in a concentration-dependent manner. Morphological observations revealed hallmark properties of apoptosis in treated cells. The methanol extract induced an increase in ROS generation and mitochondrial depolarization in MDA-MB-231 cells, suggesting its potent apoptotic activity. The present study demonstrated that the S. ferruginea methanol extract mediated MDA-MB-231 cell growth inhibition via induction of apoptosis which was confirmed by Western blot analysis. It may be a potential anticancer agent; however, its in vivo anticancer activity needs to be investigated.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27410459</pmid><doi>10.1371/journal.pone.0158942</doi><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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issn 1932-6203
1932-6203
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source Electronic Journals Library; MEDLINE; PLoS_OA刊; PubMed Central; Directory of Open Access Journals; Free Full-Text Journals in Chemistry
subjects Anticancer properties
Antioxidants
Antioxidants (Nutrients)
Antioxidants - chemistry
Antioxidants - isolation & purification
Antioxidants - metabolism
Antioxidants - pharmacology
Antitumor activity
Apoptosis
Apoptosis - drug effects
Biology and Life Sciences
Biphenyl Compounds - metabolism
Branches
Breast cancer
Breast Neoplasms - pathology
Cancer
Care and treatment
Caspase 3 - metabolism
Caspase 7 - metabolism
Catechin
Cell Line, Tumor
Cell Movement - drug effects
Cell Nucleus - drug effects
Cell Proliferation - drug effects
Chelation
Cytotoxicity
Deciduous trees
Depolarization
Drug therapy
Flavonoids - analysis
Gallic acid
Humans
In vivo methods and tests
Iron - metabolism
Loranthaceae
Medicine and Health Sciences
Membrane Potential, Mitochondrial - drug effects
Methanol
Methanol - chemistry
Mistletoes
Mitochondria
Phenolic compounds
Phenols
Phenols - analysis
Physical Sciences
Picrates - metabolism
Plant Extracts - chemistry
Plant Extracts - isolation & purification
Plant Extracts - metabolism
Plant Extracts - pharmacology
Plant Stems - chemistry
Polarity
Poly(ADP-ribose) Polymerases - metabolism
Reactive Oxygen Species - metabolism
Research and Analysis Methods
Risk factors
Santalales
Scavenging
Skin
Tracheophyta - chemistry
Viscum album
Water - chemistry
title Antioxidant Activity and ROS-Dependent Apoptotic Effect of Scurrula ferruginea (Jack) Danser Methanol Extract in Human Breast Cancer Cell MDA-MB-231
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