Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8789
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dc.contributor.authorDodurga, Yavuz-
dc.contributor.authorYonguc, G.N.-
dc.contributor.authorAvci, C.B.-
dc.contributor.authorBağcı, Gülseren-
dc.contributor.authorGunduz, Cumhur-
dc.contributor.authorSatıroğlu-Tufan, Naciye Lale-
dc.date.accessioned2019-08-16T12:47:09Z-
dc.date.available2019-08-16T12:47:09Z-
dc.date.issued2012-
dc.identifier.issn0301-4851-
dc.identifier.urihttps://hdl.handle.net/11499/8789-
dc.identifier.urihttps://doi.org/10.1007/s11033-012-2019-8-
dc.description.abstractHepatocellular carcinoma (HCC) originates from liver cells and is one of the most common malignant cancers in the world. microRNAs (miRNA), are single strand non-coding RNA molecules with the length of 18-25 nucleotides. miRNAs play an important role in the development of HCC, i.e., miRNAs have a significant impact on multistep hepatocellular carcinogenesis including cellular migration and invasion. URG4/URGCP (up-regulated gene-4/upregulator of cell proliferation) is up-regulated in the presence of HBxAg and has been identified and characterized by Satiroglu-Tufan et al. The full-length URG4/URGCP is 3.607 kb. Overexpression of URG4/URGCP in the presence of HBV X protein may function as a putative oncogene that significantly contributes to multi-step hepatocarcinogenesis. In this study, we aimed to investigate potential miRNA expression changes in HepG2 cell line model system in the presence of URG4/URGCP and in the absence of URG4/URGCP, which was suppressed by RNA interference. To functionally characterize URG4/URGCP, independent cultures of HepG2 cells were stably transfected with pcDNA3 or pcDNA3-URG4/URGCP. Relative quantification of whole genome miRNAs was analyzed by RT-PCR using human whole genome miRNA qPCR profiling kits. Among the 1,034 human miRNAs investigated by the arrays, 77 miRNAs were up-regulated and nine miRNAs were down-regulated in the presence of URG4/URGCP. In conclusion, we have analyzed miRNA profiles in HepG2 cells in presence or absence of URG4/URGCP gene using RNA interference. Some of these miRNAs may play roles in URG4/URGCP gene related disease development through the regulation of different signaling pathways. © 2012 Springer Science+Business Media Dordrecht.en_US
dc.language.isoenen_US
dc.publisherSpringer Netherlandsen_US
dc.relation.ispartofMolecular Biology Reportsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHepatocellular carcinoma cell lineen_US
dc.subjectmiRNAen_US
dc.subjectsiRNAen_US
dc.subjectURG4/URGCPen_US
dc.subjectmessenger RNAen_US
dc.subjectmicroRNAen_US
dc.subjecttumor proteinen_US
dc.subjectURG4 protein, humanen_US
dc.subjectarticleen_US
dc.subjectcell strain HepG2en_US
dc.subjectdown regulationen_US
dc.subjectgene expression profilingen_US
dc.subjectgene expression regulationen_US
dc.subjectgeneticsen_US
dc.subjecthumanen_US
dc.subjectmetabolismen_US
dc.subjectRNA interferenceen_US
dc.subjectupregulationen_US
dc.subjectDown-Regulationen_US
dc.subjectGene Expression Profilingen_US
dc.subjectGene Expression Regulation, Neoplasticen_US
dc.subjectHep G2 Cellsen_US
dc.subjectHumansen_US
dc.subjectMicroRNAsen_US
dc.subjectNeoplasm Proteinsen_US
dc.subjectRNA Interferenceen_US
dc.subjectRNA, Messengeren_US
dc.subjectUp-Regulationen_US
dc.titleInvestigation of microRNA expression changes in HepG2 cell line in presence of URG4/URGCP and in absence of URG4/URGCP suppressed by RNA interferenceen_US
dc.typeArticleen_US
dc.identifier.startpage1-
dc.identifier.startpage1en_US
dc.identifier.endpage6en_US
dc.authorid0000-0002-4936-5954-
dc.authorid0000-0001-9399-0960-
dc.identifier.doi10.1007/s11033-012-2019-8-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid23053999en_US
dc.identifier.scopus2-s2.0-85027921438en_US
dc.identifier.wosWOS:000310586700132en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.02. Internal Medicine-
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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