Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/9974
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dc.contributor.authorEroğlu, C.-
dc.contributor.authorSeçme, Mücahit.-
dc.contributor.authorBağcı, Gülseren.-
dc.contributor.authorDodurga, Yavuz-
dc.date.accessioned2019-08-16T13:08:31Z-
dc.date.available2019-08-16T13:08:31Z-
dc.date.issued2015-
dc.identifier.issn1010-4283-
dc.identifier.urihttps://hdl.handle.net/11499/9974-
dc.identifier.urihttps://doi.org/10.1007/s13277-015-3689-3-
dc.description.abstractStudies on genetic changes underlying prostate cancer and the possible signaling pathways are getting increased day by day, and new treatment methods are being searched for. The aim of the present study is to investigate the effects of ferulic acid (FA), a phenolic compound, on cell cycle, apoptosis, invasion, and colony formation in the PC-3 and LNCaP prostate cancer cells. The effect of FA on cell viability was determined via a 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) method. Total RNA was isolated with Tri Reagent. Expression of 84 genes for both cell cycle and apoptosis separately was evaluated by reverse transcriptase PCR (RT-PCR). Protein expressions were evaluated by Western blot analysis. Furthermore, apoptotic effects of FA were observed with terminal deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL) assay. Effects of FA on cell invasion and colony formation were determined using Matrigel chamber and colony assay, respectively. The half maximal inhibitory concentration (IC50) dose of FA was found to be 300 µM in PC-3 cells and 500 µM in LNCaP cells. According to RT-PCR results, it was observed that FA inhibited cell proliferation by increasing the gene expressions of ATR, ATM, CDKN1A, CDKN1B, E2F4, RB1, and TP53 and decreasing the gene expressions of CCND1, CCND2, CCND3, CDK2, CDK4, and CDK6 in PC-3 cells. On the other hand, it was seen that FA suppressed cell proliferation by increasing in the gene expressions of CASP1, CASP2, CASP8, CYCS, FAS, FASLG, and TRADD and decreasing in the gene expressions of BCL2 and XIAP in LNCaP cells. In this study, protein expression of CDK4 and BCL2 genes significantly decreased in these cells. It could induce apoptosis in PC-3 and LNCaP cells. Also, it was observed that FA suppressed the invasion in PC-3 and LNCaP cells. Moreover, it suppressed the colony formation. In conclusion, it has been observed that FA may lead to cell cycle arrest in PC-3 cells while it may cause apoptosis in LNCaP cells. © 2015, International Society of Oncology and BioMarkers (ISOBM).en_US
dc.language.isoenen_US
dc.publisherSpringer Netherlandsen_US
dc.relation.ispartofTumor Biologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectApoptosisen_US
dc.subjectCell cycleen_US
dc.subjectColony formationen_US
dc.subjectFerulic aciden_US
dc.subjectInvasionen_US
dc.subjectProstate canceren_US
dc.subjectbeta arrestin 1en_US
dc.subjectCASP1 geneen_US
dc.subjectCASP2 geneen_US
dc.subjectCASP8 geneen_US
dc.subjectCYCS geneen_US
dc.subjectdeoxyuridine triphosphate derivativeen_US
dc.subjectFAS geneen_US
dc.subjectFASLG geneen_US
dc.subjectferulic aciden_US
dc.subjectprotein bcl 2en_US
dc.subjectprotein p53en_US
dc.subjectRNAen_US
dc.subjectTRADD geneen_US
dc.subjecttranscription factor E2F4en_US
dc.subjectunclassified drugen_US
dc.subjectX linked inhibitor of apoptosisen_US
dc.subjectcoumaric aciden_US
dc.subjecttumor proteinen_US
dc.subjectantineoplastic activityen_US
dc.subjectapoptosisen_US
dc.subjectArticleen_US
dc.subjectcancer cellen_US
dc.subjectCCND1 geneen_US
dc.subjectCCND2 geneen_US
dc.subjectCCND3 geneen_US
dc.subjectCDK2 geneen_US
dc.subjectCDK4 geneen_US
dc.subjectCDK6 geneen_US
dc.subjectCDKN1A geneen_US
dc.subjectCDKN1B geneen_US
dc.subjectcell cycleen_US
dc.subjectcell cycle arresten_US
dc.subjectcell invasionen_US
dc.subjectcell proliferationen_US
dc.subjectcell viabilityen_US
dc.subjectcolony formationen_US
dc.subjectdrug mechanismen_US
dc.subjectgeneen_US
dc.subjectgene expressionen_US
dc.subjectheredityen_US
dc.subjecthumanen_US
dc.subjectIC50en_US
dc.subjectmaleen_US
dc.subjectpriority journalen_US
dc.subjectprostate canceren_US
dc.subjectprotein expressionen_US
dc.subjectreverse transcription polymerase chain reactionen_US
dc.subjectTUNEL assayen_US
dc.subjectWestern blottingen_US
dc.subjectbiosynthesisen_US
dc.subjectcell cycle checkpointen_US
dc.subjectcell survivalen_US
dc.subjectdrug effectsen_US
dc.subjectgene expression regulationen_US
dc.subjectgeneticsen_US
dc.subjectpathologyen_US
dc.subjectProstatic Neoplasmsen_US
dc.subjectsignal transductionen_US
dc.subjecttumor cell lineen_US
dc.subjecttumor invasionen_US
dc.subjectCell Cycle Checkpointsen_US
dc.subjectCell Line, Tumoren_US
dc.subjectCell Proliferationen_US
dc.subjectCell Survivalen_US
dc.subjectCoumaric Acidsen_US
dc.subjectGene Expression Regulation, Neoplasticen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectNeoplasm Invasivenessen_US
dc.subjectNeoplasm Proteinsen_US
dc.subjectSignal Transductionen_US
dc.titleAssessment of the anticancer mechanism of ferulic acid via cell cycle and apoptotic pathways in human prostate cancer cell linesen_US
dc.typeArticleen_US
dc.identifier.volume36en_US
dc.identifier.issue12en_US
dc.identifier.startpage9437-
dc.identifier.startpage9437en_US
dc.identifier.endpage9446en_US
dc.identifier.doi10.1007/s13277-015-3689-3-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid26124008en_US
dc.identifier.scopus2-s2.0-84952876408en_US
dc.identifier.wosWOS:000367329300038en_US
dc.identifier.scopusqualityQ1-
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-
Appears in Collections: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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