Lycopene activity on lung and kidney cancer cells by T2 relaxation time 1H Magnetic Resonance Imaging in vitro

dc.contributor.authorPogoda, Katarzyna
dc.contributor.authorPucka, Maria
dc.contributor.authorTabarkiewicz, Jacek
dc.contributor.authorBober, Zuzanna
dc.contributor.authorAebisher, David
dc.contributor.authorGaliniak, Sabina
dc.contributor.authorBartusik-Aebisher, Dorota
dc.date.accessioned2020-11-16T09:36:04Z
dc.date.available2020-11-16T09:36:04Z
dc.date.issued2020
dc.description.abstractIntroduction. The paper presents the results of a study of cell cultures of lung cancer and kidney cancer using lycopene performed using clinical magnetic resonance imaging. Aim. The aim of the study was to evaluate lycopene activity on tumor cell cultures. Material and methods. For this purpose, MR tests were performed using the technique of determining transverse relaxation. Results. Described here studies demonstrated that lycopene may inhibit the growth of A549 and ACHN cell lines. Conclusion. We determine changes in spin lattice relaxavity T2 to monitor treatment of lung cancer cell line A549 and kidney cancer cell line ACHN cells treatment with lycopene.pl_PL.UTF-8
dc.identifier.citationEuropean Journal of Clinical and Experimental Medicine T. 18, z. 1 (2020), s. 5–9pl_PL.UTF-8
dc.identifier.doi10.15584/ejcem.2020.1.1
dc.identifier.eissn2544-1361
dc.identifier.issn2544-2406
dc.identifier.urihttp://repozytorium.ur.edu.pl/handle/item/5771
dc.language.isoengpl_PL.UTF-8
dc.publisherWydawnictwo Uniwersytetu Rzeszowskiegopl_PL.UTF-8
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectcell culturespl_PL.UTF-8
dc.subjectlung cancerpl_PL.UTF-8
dc.subjectlycopenepl_PL.UTF-8
dc.subjectkidney cancerpl_PL.UTF-8
dc.subjectmagnetic resonance imagingpl_PL.UTF-8
dc.subjectrelaxation timespl_PL.UTF-8
dc.titleLycopene activity on lung and kidney cancer cells by T2 relaxation time 1H Magnetic Resonance Imaging in vitropl_PL.UTF-8
dc.typearticlepl_PL.UTF-8
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