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dc.contributor.authorYuzbasioglu D.
dc.contributor.authorMamur S.
dc.contributor.authorAvuloglu-Yilmaz E.
dc.contributor.authorErikel E.
dc.contributor.authorCelebi-Keskin A.
dc.contributor.authorUnal F.
dc.date.accessioned2024-03-12T19:35:16Z
dc.date.available2024-03-12T19:35:16Z
dc.date.issued2021
dc.identifier.issn13835718
dc.identifier.urihttps://doi.org/10.1016/j.mrgentox.2021.503391
dc.identifier.urihttps://hdl.handle.net/20.500.12450/2873
dc.description.abstractPullulan is a biocompatible and water-soluble exo-polysaccharide produced by primary strains of the fungus Aureobasidium pullulans. It is frequently used in the pharmaceutical and food industries. In this study, possible cytotoxic effect of pullulan was assessed using the MTT assay in the human breast cancer (MCF-7) cell line. Micronucleus (MN), micronucleus-FISH (MN-FISH), random amplified polymorphic DNA (RAPD-PCR), and comet assays were used to investigate genotoxic and antigenotoxic effects of pullulan against mitomycin C (MMC) (at MN assay) and hydrogen peroxide (at comet assay) in human lymphocytes. Antigenotoxicity was determined using two different applications: 1 h pretreatment and simultaneous treatment. In the MTT assay, pullulan significantly reduced the cell viability at 15.6?2000 ?g/mL compared to the control. No significant alterations in MN rates were found in human lymphocytes treated with different concentrations of pullulan compared to the control. In contrast, co-treatment of pullulan and MMC decreased the frequency of MN in almost all the treatment concentrations and durations compared to the MMC. No significant change was observed in the frequency of the centromere-positive C + or negative C- MNi compared to the positive control. In comet assay, pullulan did not affect comet tail intensity compared to the negative control. On the contrary, pullulan in combination with H2O2 significantly decreased tail intensity at almost all the concentrations compared to the positive control. The changes occurring in RAPD-PCR profiles following pullulan treatments included an increase or decrease in band intensity and gain or loss of bands. These results indicate that exopolysaccharide Pullulan is not genotoxic; moreover, it possesses a protective effect against MMC and H2O2 induced genotoxicity. In breast cancer cells, pullulan induced cytotoxic/anti-proliferative effect. © 2021 Elsevier B.V.en_US
dc.description.sponsorship05/2017-14en_US
dc.description.sponsorshipThis study was supported by Gazi University Research Fund under Project No: 05/2017-14 , Turkey.en_US
dc.language.isoengen_US
dc.publisherElsevier B.V.en_US
dc.relation.ispartofMutation Research - Genetic Toxicology and Environmental Mutagenesisen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectComet assayen_US
dc.subjectMicronucleus (MN)en_US
dc.subjectMN-FISHen_US
dc.subjectMTT assayen_US
dc.subjectPullulanen_US
dc.subjectRAPD-PCRen_US
dc.subjectantimutagenic agenten_US
dc.subjectglucanen_US
dc.subjectmitomycinen_US
dc.subjectmutagenic agenten_US
dc.subjectpullulanen_US
dc.subjectadolescenten_US
dc.subjectadulten_US
dc.subjectcomet assayen_US
dc.subjectDNA damageen_US
dc.subjectdrug effecten_US
dc.subjectfemaleen_US
dc.subjectfluorescence in situ hybridizationen_US
dc.subjecthumanen_US
dc.subjectlymphocyteen_US
dc.subjectmaleen_US
dc.subjectMCF-7 cell lineen_US
dc.subjectmicronucleus testen_US
dc.subjectyoung adulten_US
dc.subjectAdolescenten_US
dc.subjectAdulten_US
dc.subjectAntimutagenic Agentsen_US
dc.subjectComet Assayen_US
dc.subjectDNA Damageen_US
dc.subjectFemaleen_US
dc.subjectGlucansen_US
dc.subjectHumansen_US
dc.subjectIn Situ Hybridization, Fluorescenceen_US
dc.subjectLymphocytesen_US
dc.subjectMaleen_US
dc.subjectMCF-7 Cellsen_US
dc.subjectMicronucleus Testsen_US
dc.subjectMitomycinen_US
dc.subjectMutagensen_US
dc.subjectYoung Adulten_US
dc.titleEvaluation of the genotoxic and antigenotoxic effects of exopolysaccharide pullulan in human lymphocytes in vitroen_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.identifier.volume870-871en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85112561800en_US
dc.identifier.doi10.1016/j.mrgentox.2021.503391
dc.department-tempYuzbasioglu, D., Genetic Toxicology Laboratory, Department of Biology, Faculty of Science, Gazi University, Ankara, Turkey; Mamur, S., Life Sciences Application and Research Center, Gazi University, Ankara, Turkey; Avuloglu-Yilmaz, E., Vocational School of Technical Sciences, Amasya University, Amasya, Turkey; Erikel, E., Genetic Toxicology Laboratory, Department of Biology, Faculty of Science, Gazi University, Ankara, Turkey; Celebi-Keskin, A., Department of Bioengineering, Faculty of Engineering and Architecture, Kırıkkale University, Kırıkkale, Turkey; Unal, F., Genetic Toxicology Laboratory, Department of Biology, Faculty of Science, Gazi University, Ankara, Turkeyen_US
dc.authorscopusid6506526163
dc.authorscopusid35330424400
dc.authorscopusid57189069248
dc.authorscopusid57202961259
dc.authorscopusid37121492600
dc.authorscopusid7004407682
dc.identifier.pmid34583820en_US


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