Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/1469
DC FieldValueLanguage
dc.contributor.authorĐorđević, Jelenaen_US
dc.contributor.authorKolarević, Stoimiren_US
dc.contributor.authorJovanović, Jovanaen_US
dc.contributor.authorKostić-Vuković, Jovanaen_US
dc.contributor.authorNovaković, Irenaen_US
dc.contributor.authorJeremić, Markoen_US
dc.contributor.authorSladić, Dušanen_US
dc.contributor.authorVuković Gačić, Brankaen_US
dc.date.accessioned2019-09-27T08:12:25Z-
dc.date.available2019-09-27T08:12:25Z-
dc.date.issued2018-01-01-
dc.identifier.issn0148-0545-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/1469-
dc.description.abstract© 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group. Tert-butylquinone (TBQ) and its alkylamino and aralkylamino derivatives are of high interest as a potential antitumor agent. Therefore, it was necessary to investigate if the compounds exert undesirable activities such as interaction with DNA molecule which could result in negative side effects in the case of their use in the diseases treatment. The major aim of this study was to investigate genotoxic potential of TBQ and selected derivatives in an acellular model by using plasmid DNA, in the prokaryotic model by the SOS/umuC assay in Salmonella typhimurium TA1535/pSK1002 and in eukaryotic models by using comet assay in human fetal lung cell line (MRC-5) and human liver cancer cell line (HepG2). Results indicated that in the acellular model TBQ and its derivatives do not interact with plasmid pUC19. In the prokaryotic model, only TBQ exerted weak genotoxic potential and only at highly cytotoxic concentrations. In eukaryotic models, genotoxic potential was detected mainly at the highest concentrations of the tested substances but the effect was lower in both cell lines in comparison with benzo[a]pyrene and etoposide which were used as positive controls. Weak genotoxic potential of tested compounds recommends them as good candidates for further testing in development of new antitumor agents.en_US
dc.language.isoenen_US
dc.relation.ispartofDrug and Chemical Toxicologyen_US
dc.subjectalkylamino and aralkylamino derivativesen_US
dc.subjectTert-butylquinoneen_US
dc.subjectplasmid relaxationen_US
dc.subjectSOS/umuCen_US
dc.subjectgenotoxicityen_US
dc.subjectcomet assayen_US
dc.titleEvaluation of genotoxic potential of tert-butylquinone and its derivatives in prokaryotic and eukaryotic test modelsen_US
dc.typeArticleen_US
dc.identifier.doi10.1080/01480545.2018.1514043-
dc.identifier.pmid30257571-
dc.identifier.scopus2-s2.0-85053908360-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85053908360-
dc.description.rankM22-
dc.description.impact2.604-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Comparative Physiology and Ecophysiology-
crisitem.author.deptChair of Microbiology-
crisitem.author.deptChair of Microbiology-
crisitem.author.orcid0000-0002-6510-1027-
crisitem.author.orcid0000-0002-6938-8803-
crisitem.author.orcid0000-0001-8767-1912-
Appears in Collections:Journal Article
Show simple item record

SCOPUSTM   
Citations

5
checked on Nov 20, 2024

Page view(s)

1
checked on Nov 26, 2024

Google ScholarTM

Check

Altmetric

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.