Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/10988
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dc.contributor.authorGündoğdu, Gülşah-
dc.contributor.authorDodurga, Yavuz-
dc.contributor.authorElmas, Levent-
dc.contributor.authorYılmaz Taşçı, S.-
dc.contributor.authorKaraoğlan, E. S.-
dc.date.accessioned2019-08-16T13:34:19Z-
dc.date.available2019-08-16T13:34:19Z-
dc.date.issued2018-
dc.identifier.issn1308-8734-
dc.identifier.urihttps://hdl.handle.net/11499/10988-
dc.identifier.urihttps://doi.org/10.5152/eurasianjmed.2018.17403-
dc.description.abstractObjective: Isoorientin (ISO) is a flavonoid compound extracted from plant species. The goal of this study was to determine the potential antiproliferative effects of ISO in HT-29 human colorectal adenocarcinoma cell line in vitro, specifically on cell viability, apoptosis, and cell cycle pathways. Materials and Methods: The cytotoxic effect of ISO isolated from E. spectabilis was measured using 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) assay in HT-29 cell lines. Total RNA was isolated using Tri-Reagent protocol. The effects of ISO on apoptosis-related gene were detected using real-time polymerase chain reaction (RT-PCR). The findings were analyzed using “Delta-Delta CT” ??CT method and evaluated using a computer program. Volcano plot analysis was used for comparing groups and the data obtained were statistically analyzed using Student t test. Results: According to XTT result analysis, the 50% inhibitory concentration (IC50) value of ISO was 125 µM at the 48th h in HT-29 cells. The RT-PCR analysis in HT-29 cells showed that Cyclin D1 (CCND1), Cyclin-dependent kinase 6 (CDK6), BAX, BCL-2, Checkpoint kinase 1-2 (CHEK1, CHEK2) and Excision repair cross-complementing 1 (ERCC1) expressions were reduced in ISO-treated cells compared with those in the control group of cells. P53, P21, Caspase-3 (CASP-3), Caspase-8 (CASP-8), and Caspase-9 (CASP-9) gene expressions were increased Ataxia Telengiectasia and Rad-3 related (ATR) was activated in the ISO-treated group of cells compared with those in the control group of cells (p<0.05). Conclusion: ISO affected the proliferation of colorectal cancer (CRC) cells via cell cycle pathways. It also altered apoptosis gene expression. These results demonstrated that ISO can be a therapeutic agent for CRC treatment; however, more studies are needed to investigate its mechanism of actions. © 2018 by the Atatürk University School of Medicine.en_US
dc.language.isoenen_US
dc.publisherAVES İbrahim KARAen_US
dc.relation.ispartofEurasian Journal of Medicineen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCell cycle pathwayen_US
dc.subjectColorectal canceren_US
dc.subjectIsoorientinen_US
dc.titleInvestigation of the anticancer mechanism of isoorientin isolated from eremurus spectabilis leaves via cell cycle pathways in HT-29 human colorectal adenocarcinoma cellsen_US
dc.typeArticleen_US
dc.identifier.volume50en_US
dc.identifier.issue3en_US
dc.identifier.startpage168-
dc.identifier.startpage168en_US
dc.identifier.endpage172en_US
dc.authorid0000-0002-6865-6466-
dc.identifier.doi10.5152/eurasianjmed.2018.17403-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid30515037en_US
dc.identifier.scopus2-s2.0-85057215287en_US
dc.identifier.trdizinid298706en_US
dc.identifier.wosWOS:000450354500008en_US
dc.identifier.scopusqualityQ3-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.03. Basic Medical Sciences-
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
TR Dizin İndeksli Yayınlar Koleksiyonu / TR Dizin Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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