In vitro Antioxidant and Cytotoxic Activities of Extracts of Endemic Tanacetum erzincanense Together with Phenolic Content by LC-ESI-QTOF-MS

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Özet

In this study, phenolic composition, and in vitro biological activities of ethyl acetate (EAE) and methanol (ME) extracts obtained from the aerial parts of endemic Tanacetum erzincanense were investigated. Total phenolic and flavonoid content of the extracts were determined by Folin-Ciocalteu and aluminum chloride colorimetric methods, respectively. Antioxidant capacity of the extracts was evaluated over radical scavenging (DPPH and ABTS) and metal ion reducing power (FRAP and CUPRAC) tests. Individual phenolic compounds in ME was analyzed by high-performance liquid chromatography coupled to electrospray ionization quadrupole time-of-flight mass spectrometry (LC-ESI-QTOF/MS). Cell inhibitory potential of the extracts was tested against colorectal adenocarcinoma (HT-29), breast adenocarcinoma (MCF-7), and hepatocarcinoma (HepG2) cells by 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) assay. The results showed that ME contains higher TPC (64.4 mg GAE/g) and TFC (62.2 mg QE/g) than those of EAE (41.5 mg GAE/g and 40.0 mg QE/g). LC-ESI-QTOF/MS analysis revealed that ME is rich in phenolic compounds, namely, chlorogenic acid, apigenin, quercetin, luteolin, and diosmetin. Antioxidant assay results indicated that ME possess stronger activity than EAE and a power that competes with synthetic antioxidants. XTT assay results demonstrated that although both extracts displayed a considerable cytotoxicity against the tested cancer cell lines in a time and dose-dependent manner, ME expressed its selective inhibitory action towards MCF-7 cells with an IC50 value of 20.4 μg/mL for 72 h. These results may serve as a basis for further in vivo studies to examine the potential applications of T. erzincanense in food and pharmaceutical industries.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/gumushane/14966Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/cbdv.202000812Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorYapıcı, İsmail
dc.contributor.authorAltay, Ahmet
dc.contributor.authorÖztürk Sarıkaya, Beyza
dc.contributor.authorKorkmaz, Mustafa
dc.contributor.authorAtila, Alptuğ
dc.contributor.authorGülçin, İlhami
dc.contributor.authorKöksal, Ekrem
dc.date.accessioned2026-10-22T10:23:23.689886435Z
dc.date.available2026-10-22T10:23:23.689886435Z
dc.date.issued2021
dc.description.abstractIn this study, phenolic composition, and in vitro biological activities of ethyl acetate (EAE) and methanol (ME) extracts obtained from the aerial parts of endemic Tanacetum erzincanense were investigated. Total phenolic and flavonoid content of the extracts were determined by Folin-Ciocalteu and aluminum chloride colorimetric methods, respectively. Antioxidant capacity of the extracts was evaluated over radical scavenging (DPPH and ABTS) and metal ion reducing power (FRAP and CUPRAC) tests. Individual phenolic compounds in ME was analyzed by high-performance liquid chromatography coupled to electrospray ionization quadrupole time-of-flight mass spectrometry (LC-ESI-QTOF/MS). Cell inhibitory potential of the extracts was tested against colorectal adenocarcinoma (HT-29), breast adenocarcinoma (MCF-7), and hepatocarcinoma (HepG2) cells by 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) assay. The results showed that ME contains higher TPC (64.4 mg GAE/g) and TFC (62.2 mg QE/g) than those of EAE (41.5 mg GAE/g and 40.0 mg QE/g). LC-ESI-QTOF/MS analysis revealed that ME is rich in phenolic compounds, namely, chlorogenic acid, apigenin, quercetin, luteolin, and diosmetin. Antioxidant assay results indicated that ME possess stronger activity than EAE and a power that competes with synthetic antioxidants. XTT assay results demonstrated that although both extracts displayed a considerable cytotoxicity against the tested cancer cell lines in a time and dose-dependent manner, ME expressed its selective inhibitory action towards MCF-7 cells with an IC50 value of 20.4 μg/mL for 72 h. These results may serve as a basis for further in vivo studies to examine the potential applications of T. erzincanense in food and pharmaceutical industries.
dc.description.sponsorshipEU-BAP
dc.description.sponsorshipEU‐BAP, (FBA‐2016‐381)
dc.description.sponsorshipErzincan University Scientific Research Projects Coordination Commission
dc.identifier.articlenumbere2000812
dc.identifier.doi10.1002/cbdv.202000812
dc.identifier.eissn1612-1880
dc.identifier.issn1612-1872
dc.identifier.issue3
dc.identifier.pmid33464702
dc.identifier.scopus2-s2.0-85100612332
dc.identifier.startpagee2000812
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/14966
dc.identifier.volume18
dc.identifier.wosWOS:000615937400001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofChemistry and Biodiversity
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectantioxidant activity
dc.subjectAsteraceae
dc.subjectcytotoxicity
dc.subjectLC-ESI-QTOF/MS
dc.subjectpolyphenols
dc.subjectTanacetum erzincanense
dc.subject.classificationBiochemistry & Molecular Biology
dc.subject.classificationChemistry, Multidisciplinary
dc.subject.classificationChemistry
dc.subject.otherAntineoplastic Agents, Phytogenic
dc.subject.otherAntioxidants
dc.subject.otherCell Proliferation
dc.subject.otherChromatography, Liquid
dc.subject.otherDose-Response Relationship, Drug
dc.subject.otherDrug Screening Assays, Antitumor
dc.subject.otherHumans
dc.subject.otherPhenols
dc.subject.otherSpectrometry, Mass, Electrospray Ionization
dc.subject.otherStructure-Activity Relationship
dc.subject.otherTanacetum
dc.subject.otherTumor Cells, Cultured
dc.subject.otheracetic acid ethyl ester
dc.subject.otheraluminum chloride
dc.subject.otherantioxidant
dc.subject.otherapigenin
dc.subject.otherchlorogenic acid
dc.subject.othercytotoxic agent
dc.subject.otherdiosmetin
dc.subject.otherluteolin
dc.subject.othermethanol
dc.subject.otherphenol
dc.subject.otherplant extract
dc.subject.otherquercetin
dc.subject.otherTanacetum erzincanense extract
dc.subject.otherunclassified drug
dc.subject.otherantineoplastic agent
dc.subject.otherphenol derivative
dc.subject.otherABTS radical scavenging assay
dc.subject.otherantioxidant activity
dc.subject.otherArticle
dc.subject.otherchemical composition
dc.subject.othercolorimetry
dc.subject.otherconcentration response
dc.subject.othercontrolled study
dc.subject.otherDPPH radical scavenging assay
dc.subject.otherdrug cytotoxicity
dc.subject.otherelectrospray
dc.subject.otherferric reducing antioxidant power assay
dc.subject.otherHep-G2 cell line
dc.subject.otherhigh performance liquid chromatography
dc.subject.otherHT-29 cell line
dc.subject.otherhuman
dc.subject.otherhuman cell
dc.subject.otherIC50
dc.subject.otherin vitro study
dc.subject.otherMCF-7 cell line
dc.subject.otherTanacetum erzincanense
dc.subject.othertime of flight mass spectrometry
dc.subject.otherXTT assay
dc.subject.otherchemistry
dc.subject.otherdose response
dc.subject.otherdrug effect
dc.subject.otherdrug screening
dc.subject.otherelectrospray mass spectrometry
dc.subject.otherisolation and purification
dc.subject.otherliquid chromatography
dc.subject.otherstructure activity relation
dc.subject.othertumor cell culture
dc.titleIn vitro Antioxidant and Cytotoxic Activities of Extracts of Endemic Tanacetum erzincanense Together with Phenolic Content by LC-ESI-QTOF-MS
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex24
rdl.citation.scopus27
rdl.citation.wos24
rdl.departmentGumushane University, Faculty of Engineering and Natural Science, Department of Food Engineering, 29100, Gümüşhane, Turkey
rdl.oa.statusclosed
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)