Effective and new potent drug combination: Histone deacetylase and wnt/beta-catenin pathway inhibitors in lung carcinoma cells

dc.contributor.authorErkisa, Merve
dc.contributor.buuauthorAkgün, Oğuzhan
dc.contributor.buuauthorArı, Ferda
dc.contributor.departmentBursa Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji, Moleküler Biyoloji Bölümü.tr_TR
dc.contributor.orcid0000-0002-8410-1786tr_TR
dc.contributor.orcid0000-0002-6729-7908tr_TR
dc.contributor.researcheridA-5608-2019tr_TR
dc.contributor.researcheridAAG-7012-2021tr_TR
dc.contributor.scopusid57194269996tr_TR
dc.contributor.scopusid24376085300tr_TR
dc.date.accessioned2024-02-09T07:31:37Z
dc.date.available2024-02-09T07:31:37Z
dc.date.issued2019-09
dc.description.abstractLung cancer is the most commonly diagnosed cancer worldwide with a high mortality rate. In this study, the therapeutic effect of combination valproic acid and niclosamide was investigated on human lung cancer cell line. The effects of the compounds alone and combination therapy on cell viability were determined by sulforhodamine B and adenosine 5 '-triphosphate viability assays. Flow cytometry was used to determine the cell death mechanism and DNA damage levels responsible for the cytotoxic effects of combination therapy. The presence of apoptosis in cells was supported by fluorescence microscopy and also by using inhibitors of the apoptotic signaling pathway. The increase in cellular reactive oxygen species (ROS) level in combination therapy was determined by H2DCFDA staining. The effect of N-acetyl-l-cysteine combination on ROS increase was investigated on cell viability. In addition, the expression levels of the proteins associated with epigenetic regulation and cell death were analyzed by Western blotting and gene expression levels were determined using real-time quantitative polymerase chain reaction.It was observed that the combination therapy showed a cytotoxic effect on the A549 lung cancer cells compared to the individual use of the inhibitors. The absence of this effect on normal lung cells revealed the presence of a selective toxic effect. When the mechanism of cytotoxicity is examined, it has been observed that combination therapy initiates the activation of tumor necrosis receptors and causes apoptosis by activated caspase. It was also observed that this extrinsic apoptotic pathway was activated on the mitochondrial pathway. In addition, ER stress and mitochondrial membrane potential loss associated with increased ROS levels induce cell death. When the data in this study were evaluated, combination therapy caused a dramatic decrease in cell viability by inducing the extrinsic apoptotic pathway in lung cancer cell line. Therefore, it was concluded that it can be used as an effective and new treatment option for lung cancer.en_US
dc.identifier.citationAkgün, O. ve Arı, F. (2019). ''Effective and new potent drug combination: Histone deacetylase and wnt/beta-catenin pathway inhibitors in lung carcinoma cells''. Journal of Cellular Biochemistry, 120(9), 15467-15482.en_US
dc.identifier.endpage15482tr_TR
dc.identifier.issn0730-2312
dc.identifier.issn1097-4644
dc.identifier.issue9tr_TR
dc.identifier.pubmed31037769tr_TR
dc.identifier.scopus2-s2.0-85069524183tr_TR
dc.identifier.startpage15467tr_TR
dc.identifier.urihttps://doi.org/10.1002/jcb.28813en_US
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/jcb.28813en_US
dc.identifier.urihttps://hdl.handle.net/11452/39606en_US
dc.identifier.volume120en_US
dc.identifier.wos000476804200119
dc.indexed.pubmedPubMeden_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.bapOUAP (F)-2015/15en_US
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationSanayitr_TR
dc.relation.journalJournal of Cellular Biochemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiochemistry & bolecular biologyen_US
dc.subjectCell biologyen_US
dc.subjectApoptosisen_US
dc.subjectLung canceren_US
dc.subjectNiclosamideen_US
dc.subjectValproic aciden_US
dc.subjectEndoplasmic-reticulum stressen_US
dc.subjectValproic aciden_US
dc.subjectGrowth-inhibitionen_US
dc.subjectTargeted Therapyen_US
dc.subjectDown-regulationen_US
dc.subjectUp-regulationen_US
dc.subjectCancer cellsen_US
dc.subjectIn-vitroen_US
dc.subjectNiclosamideen_US
dc.subjectApoptosisen_US
dc.subject.emtreeAcetylcysteineen_US
dc.subject.emtreeAdenosine triphosphateen_US
dc.subject.emtreeCaspase 3en_US
dc.subject.emtreeCaspase 7en_US
dc.subject.emtreeCaspase 8en_US
dc.subject.emtreeCytokeratin 18en_US
dc.subject.emtreeHistone deacetylaseen_US
dc.subject.emtreeHistone deacetylase 1en_US
dc.subject.emtreeHistone deacetylase 2en_US
dc.subject.emtreeHistone H3en_US
dc.subject.emtreeNiclosamideen_US
dc.subject.emtreeReactive oxygen metaboliteen_US
dc.subject.emtreeValproic aciden_US
dc.subject.emtreeAntineoplastic agenten_US
dc.subject.emtreeHistone deacetylase inhibitoren_US
dc.subject.emtreeNiclosamideen_US
dc.subject.emtreeReactive oxygen metaboliteen_US
dc.subject.emtreeValproic aciden_US
dc.subject.emtreeA-549 cell lineen_US
dc.subject.emtreeAntineoplastic activityen_US
dc.subject.emtreeApoptosisen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBronchial cell lineen_US
dc.subject.emtreeCell densityen_US
dc.subject.emtreeCell viabilityen_US
dc.subject.emtreeCombination drug therapyen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDNA damageen_US
dc.subject.emtreeDrug cytotoxicityen_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeDrug potencyen_US
dc.subject.emtreeEndoplasmic reticulum stressen_US
dc.subject.emtreeFlow cytometryen_US
dc.subject.emtreeFluorescence microscopyen_US
dc.subject.emtreeGene expression levelen_US
dc.subject.emtreeHistone acetylationen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeIc50en_US
dc.subject.emtreeLung carcinomaen_US
dc.subject.emtreeMitochondrial membrane potentialen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeWnt signalingen_US
dc.subject.emtreeCell proliferationen_US
dc.subject.emtreeCell survivalen_US
dc.subject.emtreeDrug effecten_US
dc.subject.emtreeDrug potentiationen_US
dc.subject.emtreeGenetic epigenesisen_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreeLung tumoren_US
dc.subject.emtreeMetabolismen_US
dc.subject.emtreeTumor cell lineen_US
dc.subject.emtreeWnt signalingen_US
dc.subject.meshA549 cellsen_US
dc.subject.meshAntineoplastic combined chemotherapy protocolsen_US
dc.subject.meshCell line, tumoren_US
dc.subject.meshCell proliferationen_US
dc.subject.meshCell survivalen_US
dc.subject.meshDNA damageen_US
dc.subject.meshDrug synergismen_US
dc.subject.meshEpigenesis, geneticen_US
dc.subject.meshHistone deacetylase inhibitorsen_US
dc.subject.meshHumansen_US
dc.subject.meshLung neoplasmsen_US
dc.subject.meshMembrane potentialen_US
dc.subject.meshMitochondrialen_US
dc.subject.meshNiclosamideen_US
dc.subject.meshReactive oxygen speciesen_US
dc.subject.meshValproic aciden_US
dc.subject.meshWnt signaling pathwayen_US
dc.subject.scopusApoptosis; Pyrvinium Embonate; Cestode Infectionsen_US
dc.subject.wosBiochemistry & molecular biologyen_US
dc.subject.wosCell biologyen_US
dc.titleEffective and new potent drug combination: Histone deacetylase and wnt/beta-catenin pathway inhibitors in lung carcinoma cellsen_US
dc.typeArticleen_US
dc.wos.quartileQ2en_US

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