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dc.creatorPesic, Milica
dc.creatorPodolski-Renic, Ana
dc.creatorStojković, Sonja
dc.creatorMatović, Branko
dc.creatorZmejkoski, Danica
dc.creatorKojić, Vesna
dc.creatorBogdanović, Gordana
dc.creatorPavicević, Aleksandra
dc.creatorMojović, Miloš
dc.creatorSavić, Aleksandar G
dc.creatorMilenković, Ivana
dc.creatorKalauzi, Aleksandar
dc.creatorRadotić, Ksenija
dc.date.accessioned2022-04-05T15:00:20Z
dc.date.available2022-04-05T15:00:20Z
dc.date.issued2015
dc.identifier.issn0009-2797
dc.identifier.urihttp://rimsi.imsi.bg.ac.rs/handle/123456789/931
dc.description.abstractData on medical applications of cerium oxide nanoparticles CeO2 (CONP) are promising, yet information regarding their action in cells is incomplete and there are conflicting reports about in vitro toxicity. Herein, we have studied cytotoxic effect of CONP in several cancer and normal cell lines and their potential to change intracellular redox status. The IC50 was achieved only in two of eight tested cell lines, melanoma 518A2 and colorectal adenocarcinoma HT-29. Self-propagating room temperature method was applied to produce CONP with an average crystalline size of 4 nm. The results confirmed presence of Ce3+ and O2- vacancies. The induction of cell death by CONP and the production of reactive oxygen species (ROS) were analyzed by flow-cytometry. Free radicals related antioxidant capacity of the cells was studied by the reduction of stable free radical TEMPONE using electron spin resonance spectroscopy. CONP showed low or moderate cytotoxicity in cancer cell lines: adenocarcinoma DLD1 and multi-drug resistant DLD1-TxR, non-small cell lung carcinoma NCI-H460 and multi-drug resistant NCI-H460/R, while normal cell lines (keratinocytes HaCaT, lung fetal fibroblasts MRC-5) were insensitive. The most sensitive were 518A2 melanoma and HT-29 colorectal adenocarcinoma cell lines, with the IC50 values being between 100 and 200 mu M. Decreased rate of TEMPONE reduction and increased production of certain ROS species (peroxynitrite and hydrogen peroxide anion) indicates that free radical metabolism, thus redox status was changed, and antioxidant capacity damaged in the CONP treated 518A2 and HT-29 cells. In conclusion, changes in intracellular redox status induced by CONP are partly attributed to the prooxidant activity of the nanoparticles. Further, ROS induced cell damages might eventually lead to the cell death. However, low inhibitory potential of CONP in the other human cell lines tested indicates that CONP may be safe for human usage in industry and medicine.en
dc.publisherElsevier Ireland Ltd, Clare
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/45012/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/41031/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/41005/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/45005/RS//
dc.rightsrestrictedAccess
dc.sourceChemico-Biological Interactions
dc.subjectOxygen vacanciesen
dc.subjectFree radicalsen
dc.subjectFlow cytometryen
dc.subjectElectron spin resonance spectroscopyen
dc.subjectCytotoxicityen
dc.subjectCerium oxideen
dc.titleAnti-cancer effects of cerium oxide nanoparticles and its intracellular redox activityen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage93
dc.citation.other232: 85-93
dc.citation.rankM22
dc.citation.spage85
dc.citation.volume232
dc.identifier.doi10.1016/j.cbi.2015.03.013
dc.identifier.pmid25813935
dc.identifier.scopus2-s2.0-84925815621
dc.identifier.wos000353741300011
dc.type.versionpublishedVersion


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