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https://hdl.handle.net/11499/10988
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Gündoğdu, Gülşah | - |
dc.contributor.author | Dodurga, Yavuz | - |
dc.contributor.author | Elmas, Levent | - |
dc.contributor.author | Yılmaz Taşçı, S. | - |
dc.contributor.author | Karaoğlan, E. S. | - |
dc.date.accessioned | 2019-08-16T13:34:19Z | - |
dc.date.available | 2019-08-16T13:34:19Z | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 1308-8734 | - |
dc.identifier.uri | https://hdl.handle.net/11499/10988 | - |
dc.identifier.uri | https://doi.org/10.5152/eurasianjmed.2018.17403 | - |
dc.description.abstract | Objective: 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.iso | en | en_US |
dc.publisher | AVES İbrahim KARA | en_US |
dc.relation.ispartof | Eurasian Journal of Medicine | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Cell cycle pathway | en_US |
dc.subject | Colorectal cancer | en_US |
dc.subject | Isoorientin | en_US |
dc.title | Investigation of the anticancer mechanism of isoorientin isolated from eremurus spectabilis leaves via cell cycle pathways in HT-29 human colorectal adenocarcinoma cells | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 50 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.startpage | 168 | - |
dc.identifier.startpage | 168 | en_US |
dc.identifier.endpage | 172 | en_US |
dc.authorid | 0000-0002-6865-6466 | - |
dc.identifier.doi | 10.5152/eurasianjmed.2018.17403 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 30515037 | en_US |
dc.identifier.scopus | 2-s2.0-85057215287 | en_US |
dc.identifier.trdizinid | 298706 | en_US |
dc.identifier.wos | WOS:000450354500008 | en_US |
dc.identifier.scopusquality | Q3 | - |
dc.owner | Pamukkale University | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.fulltext | With Fulltext | - |
item.grantfulltext | open | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
crisitem.author.dept | 14.03. 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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File | Size | Format | |
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Investigation.pdf | 241.81 kB | Adobe PDF | View/Open |
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