In vitro Antioxidant and Cytotoxic Activities of Extracts of Endemic Tanacetum erzincanense Together with Phenolic Content by LC-ESI-QTOF-MS
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
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Yapıcı, İsmail | |
| dc.contributor.author | Altay, Ahmet | |
| dc.contributor.author | Öztürk Sarıkaya, Beyza | |
| dc.contributor.author | Korkmaz, Mustafa | |
| dc.contributor.author | Atila, Alptuğ | |
| dc.contributor.author | Gülçin, İlhami | |
| dc.contributor.author | Köksal, Ekrem | |
| dc.date.accessioned | 2026-10-22T10:23:23.689886435Z | |
| dc.date.available | 2026-10-22T10:23:23.689886435Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | 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. | |
| dc.description.sponsorship | EU-BAP | |
| dc.description.sponsorship | EU‐BAP, (FBA‐2016‐381) | |
| dc.description.sponsorship | Erzincan University Scientific Research Projects Coordination Commission | |
| dc.identifier.articlenumber | e2000812 | |
| dc.identifier.doi | 10.1002/cbdv.202000812 | |
| dc.identifier.eissn | 1612-1880 | |
| dc.identifier.issn | 1612-1872 | |
| dc.identifier.issue | 3 | |
| dc.identifier.pmid | 33464702 | |
| dc.identifier.scopus | 2-s2.0-85100612332 | |
| dc.identifier.startpage | e2000812 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/gumushane/14966 | |
| dc.identifier.volume | 18 | |
| dc.identifier.wos | WOS:000615937400001 | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Inc | |
| dc.relation.ispartof | Chemistry and Biodiversity | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | antioxidant activity | |
| dc.subject | Asteraceae | |
| dc.subject | cytotoxicity | |
| dc.subject | LC-ESI-QTOF/MS | |
| dc.subject | polyphenols | |
| dc.subject | Tanacetum erzincanense | |
| dc.subject.classification | Biochemistry & Molecular Biology | |
| dc.subject.classification | Chemistry, Multidisciplinary | |
| dc.subject.classification | Chemistry | |
| dc.subject.other | Antineoplastic Agents, Phytogenic | |
| dc.subject.other | Antioxidants | |
| dc.subject.other | Cell Proliferation | |
| dc.subject.other | Chromatography, Liquid | |
| dc.subject.other | Dose-Response Relationship, Drug | |
| dc.subject.other | Drug Screening Assays, Antitumor | |
| dc.subject.other | Humans | |
| dc.subject.other | Phenols | |
| dc.subject.other | Spectrometry, Mass, Electrospray Ionization | |
| dc.subject.other | Structure-Activity Relationship | |
| dc.subject.other | Tanacetum | |
| dc.subject.other | Tumor Cells, Cultured | |
| dc.subject.other | acetic acid ethyl ester | |
| dc.subject.other | aluminum chloride | |
| dc.subject.other | antioxidant | |
| dc.subject.other | apigenin | |
| dc.subject.other | chlorogenic acid | |
| dc.subject.other | cytotoxic agent | |
| dc.subject.other | diosmetin | |
| dc.subject.other | luteolin | |
| dc.subject.other | methanol | |
| dc.subject.other | phenol | |
| dc.subject.other | plant extract | |
| dc.subject.other | quercetin | |
| dc.subject.other | Tanacetum erzincanense extract | |
| dc.subject.other | unclassified drug | |
| dc.subject.other | antineoplastic agent | |
| dc.subject.other | phenol derivative | |
| dc.subject.other | ABTS radical scavenging assay | |
| dc.subject.other | antioxidant activity | |
| dc.subject.other | Article | |
| dc.subject.other | chemical composition | |
| dc.subject.other | colorimetry | |
| dc.subject.other | concentration response | |
| dc.subject.other | controlled study | |
| dc.subject.other | DPPH radical scavenging assay | |
| dc.subject.other | drug cytotoxicity | |
| dc.subject.other | electrospray | |
| dc.subject.other | ferric reducing antioxidant power assay | |
| dc.subject.other | Hep-G2 cell line | |
| dc.subject.other | high performance liquid chromatography | |
| dc.subject.other | HT-29 cell line | |
| dc.subject.other | human | |
| dc.subject.other | human cell | |
| dc.subject.other | IC50 | |
| dc.subject.other | in vitro study | |
| dc.subject.other | MCF-7 cell line | |
| dc.subject.other | Tanacetum erzincanense | |
| dc.subject.other | time of flight mass spectrometry | |
| dc.subject.other | XTT assay | |
| dc.subject.other | chemistry | |
| dc.subject.other | dose response | |
| dc.subject.other | drug effect | |
| dc.subject.other | drug screening | |
| dc.subject.other | electrospray mass spectrometry | |
| dc.subject.other | isolation and purification | |
| dc.subject.other | liquid chromatography | |
| dc.subject.other | structure activity relation | |
| dc.subject.other | tumor cell culture | |
| dc.title | In vitro Antioxidant and Cytotoxic Activities of Extracts of Endemic Tanacetum erzincanense Together with Phenolic Content by LC-ESI-QTOF-MS | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.openalex | 24 | |
| rdl.citation.scopus | 27 | |
| rdl.citation.wos | 24 | |
| rdl.department | Gumushane University, Faculty of Engineering and Natural Science, Department of Food Engineering, 29100, Gümüşhane, Turkey | |
| rdl.oa.status | closed | |
| rdl.sdg | SDG03 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |

