Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/10946
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dc.contributor.authorSeçme, Mücahit-
dc.contributor.authorKaygusuz, Oğuzhan-
dc.contributor.authorEroğlu, C.-
dc.contributor.authorDodurga, Yavuz-
dc.contributor.authorÇolak, Ö.F.-
dc.contributor.authorAtmaca, P.-
dc.date.accessioned2019-08-16T13:34:03Z
dc.date.available2019-08-16T13:34:03Z
dc.date.issued2018-
dc.identifier.issn1521-9437-
dc.identifier.urihttps://hdl.handle.net/11499/10946-
dc.identifier.urihttps://doi.org/10.1615/IntJMedMushrooms.2018028589-
dc.description.abstractMushrooms comprise an unlimited source of active compounds that have beneficial health effects without known negative side effects and can potentially be used as important therapeutic products against cancer, which is the leading cause of death worldwide. In this study we investigated the cytotoxic, antiproliferative, apoptotic, and anti-invasion effects of Macrolepiota procera, which is valued as an edible and medicinal mushroom, on A549 lung cancer cells. The cytotoxic effect of the M. procera extract was determined by using the XTT method. Total RNA was isolated from cells with TRI Reagent to determine the apoptotic effect of the extract, after which complementary DNA was synthesized. Expression profiles of the target genes were determined by quantitative reverse-transcriptase polymerase chain reaction, and protein changes were determined by using Western blotting. We used the TUNEL assay to evaluate the apoptotic effects of the M. procera extract. Effects of M. procera on cell invasion were investigated by using a Matrigel chamber assay. The half-maximal inhibitory concentration of the M. procera extract was determined to be 2 mg/mL against A549 lung cancer cells at 72 hours. According to our results, expression of Cyclin Dl, CDK4, CDK6, Bcl-2, Akt, and NOXA genes significantly decreased and that of Bax, Caspase-3, Caspase-9, PTEN, PUMA, p21, and p53 increased in cells from the dose group compared with their expression in control cells. According to the results of the TUNEL assay, 28 ± 3.6% of cells were apoptotic in the dose group. The M. procera extract also reduced invasion in A549 cancer cells. The results suggest that M. procera has an antiproliferative effect in a dose- and time-dependent manner. © 2018 Begell House, Inc.en_US
dc.language.isoenen_US
dc.publisherBegell House Inc.en_US
dc.relation.ispartofInternational Journal of Medicinal Mushroomsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectA549 cellsen_US
dc.subjectAnticancer activityen_US
dc.subjectApoptosisen_US
dc.subjectMacrolepiota proceraen_US
dc.subjectMedicinal mushroomsen_US
dc.subjectcaspase 3en_US
dc.subjectcaspase 9en_US
dc.subjectcyclin D1en_US
dc.subjectcyclin dependent kinase 4en_US
dc.subjectcyclin dependent kinase 6en_US
dc.subjectfungal extracten_US
dc.subjectMacrolepiota procera extracten_US
dc.subjectmessenger RNAen_US
dc.subjectphosphatidylinositol 3,4,5 trisphosphate 3 phosphataseen_US
dc.subjectprotein Baxen_US
dc.subjectprotein bcl 2en_US
dc.subjectprotein kinase Ben_US
dc.subjectprotein Noxaen_US
dc.subjectprotein p21en_US
dc.subjectprotein p53en_US
dc.subjectPUMA proteinen_US
dc.subjectunclassified drugen_US
dc.subjectantineoplastic agenten_US
dc.subjectA-549 cell lineen_US
dc.subjectantineoplastic activityen_US
dc.subjectantiproliferative activityen_US
dc.subjectapoptosisen_US
dc.subjectArticleen_US
dc.subjectBasidiomycetesen_US
dc.subjectbasidiosporeen_US
dc.subjectcell cultureen_US
dc.subjectcell cycle arresten_US
dc.subjectcell invasion assayen_US
dc.subjectcell migrationen_US
dc.subjectcontrolled studyen_US
dc.subjectcytotoxicityen_US
dc.subjectdown regulationen_US
dc.subjectfluorescence microscopyen_US
dc.subjectgene expressionen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectinhibitory concentrationen_US
dc.subjectmatrigel chamber assayen_US
dc.subjectmorphologyen_US
dc.subjectnonhumanen_US
dc.subjectprotein expressionen_US
dc.subjectreal time polymerase chain reactionen_US
dc.subjectreverse transcription polymerase chain reactionen_US
dc.subjectRNA isolationen_US
dc.subjectTUNEL assayen_US
dc.subjectupregulationen_US
dc.subjectWestern blottingen_US
dc.subjectXTT assayen_US
dc.subjectAgaricalesen_US
dc.subjectcell motionen_US
dc.subjectcell survivalen_US
dc.subjectchemistryen_US
dc.subjectdrug effecten_US
dc.subjecttumor invasionen_US
dc.subjectA549 Cellsen_US
dc.subjectAntineoplastic Agentsen_US
dc.subjectBasidiomycotaen_US
dc.subjectCell Movementen_US
dc.subjectCell Survivalen_US
dc.subjectHumansen_US
dc.subjectNeoplasm Invasivenessen_US
dc.titlePotential anticancer activity of the parasol mushroom, macrolepiota rocera(Agaricomycetes), against the A549 human lung cancer cell lineen_US
dc.typeArticleen_US
dc.identifier.volume20en_US
dc.identifier.issue11en_US
dc.identifier.startpage1075
dc.identifier.startpage1075en_US
dc.identifier.endpage1086en_US
dc.identifier.doi10.1615/IntJMedMushrooms.2018028589-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid30806231en_US
dc.identifier.scopus2-s2.0-85060384962en_US
dc.identifier.wosWOS:000449290500005en_US
dc.identifier.scopusqualityQ3-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept25.02. Plant and Animal Production-
crisitem.author.dept14.03. Basic Medical Sciences-
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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