Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8246
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dc.contributor.authorŞen, Alaattin-
dc.contributor.authorAtmaca, Pelin-
dc.contributor.authorTerzioğlu, Gülsüm-
dc.contributor.authorArslan, Şevki-
dc.date.accessioned2019-08-16T12:37:33Z
dc.date.available2019-08-16T12:37:33Z
dc.date.issued2013-
dc.identifier.issn1934-578X-
dc.identifier.urihttps://hdl.handle.net/11499/8246-
dc.description.abstractAmong hydroxycinnamic acids, caffeic, ferulic and p-coumaric acids have received considerable attention due to their biological activities. However, studies related to the biological activities of o-coumaric acid (OCA) are limited. In this regard, this study was designed to determine the chemopreventive potential of OCA in human breast cancer cells (MCF-7). The EC50 value of OCA was found to be 4.95 mM and was used throughout the study. Caspase-3 protein and mRNA levels increased by 59% and 72%. Similarly, protein and mRNA levels of Bax were increased by 115% and 152%. However, OCA treatment caused 48% and 35% decreases in Bcl-2 protein and mRNA levels. Cyclin D1 and cyclin dependent kinase-2 protein and mRNA levels decreased significantly. Moreover, p53 protein and mRNA levels increased by 178% and 245%, respectively. In addition to p53, PTEN protein and mRNA levels were induced. Although, CYP1A1, CYP1A2 and CY2E1 mRNA levels increased, CYP3A4 and CYP2C9 mRNA levels decreased in response to OCA treatment. These results suggest that OCA demonstrates anticarcinogenic activity on MCF-7 cells by activating multiple pathways. However, it also has high carcinogen activating and drug interaction potential. Therefore, serious precautions must be taken before using OCA.en_US
dc.language.isoenen_US
dc.publisherNatural Product Incorporationen_US
dc.relation.ispartofNatural Product Communicationsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectApoptosisen_US
dc.subjectCarcinogen activationen_US
dc.subjectCell cycle arrestsen_US
dc.subjectDrug interaction.en_US
dc.subjecto-Coumaric aciden_US
dc.subjectTumor suppressorsen_US
dc.subjectcaspase 3en_US
dc.subjectcoumaric aciden_US
dc.subjectcyclin dependent kinase 1en_US
dc.subjectcyclin dependent kinase 2en_US
dc.subjectcytochrome P450 1A1en_US
dc.subjectcytochrome P450 1A2en_US
dc.subjectcytochrome P450 2C9en_US
dc.subjectcytochrome P450 2E1en_US
dc.subjectcytochrome P450 3A4en_US
dc.subjectmessenger RNAen_US
dc.subjectphosphatidylinositol 3,4,5 trisphosphate 3 phosphataseen_US
dc.subjectprotein Baxen_US
dc.subjectprotein p53en_US
dc.subjectantineoplastic activityen_US
dc.subjectarticleen_US
dc.subjectcarcinogenic activityen_US
dc.subjectcell proliferationen_US
dc.subjectchemoprophylaxisen_US
dc.subjectconcentration responseen_US
dc.subjectcontrolled studyen_US
dc.subjectcytotoxicity assayen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectMCF 7 cell lineen_US
dc.subjectprotein expressionen_US
dc.subjectprotein inductionen_US
dc.titleAnticarcinogenic effect and carcinogenic potential of the dietary phenolic acid: o-Coumaric aciden_US
dc.typeArticleen_US
dc.identifier.volume8en_US
dc.identifier.issue9en_US
dc.identifier.startpage1269
dc.identifier.startpage1269en_US
dc.identifier.endpage1274en_US
dc.authorid0000-0002-8444-376-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid24273864en_US
dc.identifier.scopus2-s2.0-84886832568en_US
dc.identifier.wosWOS:000326858000022en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeArticle-
crisitem.author.dept17.02. Biology-
crisitem.author.dept17.02. Biology-
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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