Publication:
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.departmentFen Edebiyat Fakültesi
dc.contributor.departmentBiyoloji, Moleküler Biyoloji Bölümü
dc.contributor.orcid0000-0002-8410-1786
dc.contributor.orcid0000-0002-6729-7908
dc.contributor.researcheridA-5608-2019
dc.contributor.researcheridAAG-7012-2021
dc.contributor.scopusid57194269996
dc.contributor.scopusid24376085300
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.
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.
dc.identifier.endpage15482
dc.identifier.issn0730-2312
dc.identifier.issn1097-4644
dc.identifier.issue9
dc.identifier.pubmed31037769
dc.identifier.scopus2-s2.0-85069524183
dc.identifier.startpage15467
dc.identifier.urihttps://doi.org/10.1002/jcb.28813
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/jcb.28813
dc.identifier.urihttps://hdl.handle.net/11452/39606
dc.identifier.volume120
dc.identifier.wos000476804200119
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherWiley
dc.relation.bapOUAP (F)-2015/15
dc.relation.collaborationYurt içi
dc.relation.collaborationSanayi
dc.relation.journalJournal of Cellular Biochemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBiochemistry & bolecular biology
dc.subjectCell biology
dc.subjectApoptosis
dc.subjectLung cancer
dc.subjectNiclosamide
dc.subjectValproic acid
dc.subjectEndoplasmic-reticulum stress
dc.subjectValproic acid
dc.subjectGrowth-inhibition
dc.subjectTargeted Therapy
dc.subjectDown-regulation
dc.subjectUp-regulation
dc.subjectCancer cells
dc.subjectIn-vitro
dc.subjectNiclosamide
dc.subjectApoptosis
dc.subject.emtreeAcetylcysteine
dc.subject.emtreeAdenosine triphosphate
dc.subject.emtreeCaspase 3
dc.subject.emtreeCaspase 7
dc.subject.emtreeCaspase 8
dc.subject.emtreeCytokeratin 18
dc.subject.emtreeHistone deacetylase
dc.subject.emtreeHistone deacetylase 1
dc.subject.emtreeHistone deacetylase 2
dc.subject.emtreeHistone H3
dc.subject.emtreeNiclosamide
dc.subject.emtreeReactive oxygen metabolite
dc.subject.emtreeValproic acid
dc.subject.emtreeAntineoplastic agent
dc.subject.emtreeHistone deacetylase inhibitor
dc.subject.emtreeNiclosamide
dc.subject.emtreeReactive oxygen metabolite
dc.subject.emtreeValproic acid
dc.subject.emtreeA-549 cell line
dc.subject.emtreeAntineoplastic activity
dc.subject.emtreeApoptosis
dc.subject.emtreeArticle
dc.subject.emtreeBronchial cell line
dc.subject.emtreeCell density
dc.subject.emtreeCell viability
dc.subject.emtreeCombination drug therapy
dc.subject.emtreeControlled study
dc.subject.emtreeDNA damage
dc.subject.emtreeDrug cytotoxicity
dc.subject.emtreeDrug efficacy
dc.subject.emtreeDrug potency
dc.subject.emtreeEndoplasmic reticulum stress
dc.subject.emtreeFlow cytometry
dc.subject.emtreeFluorescence microscopy
dc.subject.emtreeGene expression level
dc.subject.emtreeHistone acetylation
dc.subject.emtreeHuman
dc.subject.emtreeHuman cell
dc.subject.emtreeIc50
dc.subject.emtreeLung carcinoma
dc.subject.emtreeMitochondrial membrane potential
dc.subject.emtreePriority journal
dc.subject.emtreeWnt signaling
dc.subject.emtreeCell proliferation
dc.subject.emtreeCell survival
dc.subject.emtreeDrug effect
dc.subject.emtreeDrug potentiation
dc.subject.emtreeGenetic epigenesis
dc.subject.emtreeGenetics
dc.subject.emtreeLung tumor
dc.subject.emtreeMetabolism
dc.subject.emtreeTumor cell line
dc.subject.emtreeWnt signaling
dc.subject.meshA549 cells
dc.subject.meshAntineoplastic combined chemotherapy protocols
dc.subject.meshCell line, tumor
dc.subject.meshCell proliferation
dc.subject.meshCell survival
dc.subject.meshDNA damage
dc.subject.meshDrug synergism
dc.subject.meshEpigenesis, genetic
dc.subject.meshHistone deacetylase inhibitors
dc.subject.meshHumans
dc.subject.meshLung neoplasms
dc.subject.meshMembrane potential
dc.subject.meshMitochondrial
dc.subject.meshNiclosamide
dc.subject.meshReactive oxygen species
dc.subject.meshValproic acid
dc.subject.meshWnt signaling pathway
dc.subject.scopusApoptosis; Pyrvinium Embonate; Cestode Infections
dc.subject.wosBiochemistry & molecular biology
dc.subject.wosCell biology
dc.titleEffective and new potent drug combination: Histone deacetylase and wnt/beta-catenin pathway inhibitors in lung carcinoma cells
dc.typeArticle
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Biyoloji, Moleküler Biyoloji Bölümü
local.indexed.atWOS
local.indexed.atScopus

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