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dc.contributor.author Murányi, József
dc.contributor.author Varga, Attila
dc.contributor.author Gurbi, Bianka
dc.contributor.author Gyulavári, Pál
dc.contributor.author Mező, Gábor
dc.contributor.author Vántus, Tibor
dc.date.accessioned 2021-03-04T08:52:32Z
dc.date.available 2021-03-04T08:52:32Z
dc.date.issued 2017
dc.identifier 85017239281
dc.identifier.citation journalVolume=2017;journalIssueNumber=121;journalTitle=JOVE-JOURNAL OF VISUALIZED EXPERIMENTS;pagination=e55529, pages: 9;;journalAbbreviatedTitle=JOVE-J VIS EXP;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/7569
dc.identifier.uri doi:10.3791/55529
dc.description.abstract GnRH analogues are effective targeting moieties and able to deliver anticancer agents selectively into malignant tumor cells which highly express GnRH receptors. However, the quantitative analysis of GnRH analogues’ cellular uptake and the investigated cell types in GnRH-based drug delivery systems are currently limited. Previously introduced, selectively labeled fluorescent GnRH I, -II and -III derivatives provide great detectability, and they have suitable chemical properties for reproducible and robust experiments. We also found that the appropriate up-to-date methods with these labeled GnRH analogues could offer novel information about the GnRH-based drug delivery systems. This manuscript introduces some simple and fast experiments regarding the cellular uptake of [D-Lys6(FITC)]-GnRH-I, [D-Lys6(FITC)]-GnRH-II and [Lys8(FITC)]-GnRH-III on the EBC-1 (lung), the BxPC-3 (pancreas) and on the Detroit-562- (pharynx) malignant tumor cells. In parallel with these GnRH-FITC conjugates, the cell surface level of GnRH-I receptors was also examined on these cell lines before and after the GnRH treatment by confocal laser scanning microscopy. The cellular uptake of GnRH-FITC conjugates was quantified by fluorescence-activated cell sorting. In these experiments minor differences among GnRH analogues and major differences among cell types was observed. The significant differences among cell lines are correlated with their distinct level of cell surface GnRH-I receptors. The introduced experiments contain practical methods to visualize, quantify and compare the uptake efficiency of GnRH-FITC conjugates in a time- and concentration-dependent manner on various adherent cell cultures. These results could predict the drug targeting efficiency of GnRH conjugates on the given cell culture, and offer a good basis for further experiments in the examination of GnRH-based drug delivery systems. © 2017 Journal of Visualized Experiments.
dc.format.extent e55529-e55529
dc.relation.ispartof urn:issn:1940-087X
dc.title In vitro imaging and quantification of the drug targeting efficiency of fluorescently labeled GnRH analogues
dc.type Journal Article
dc.date.updated 2019-09-02T15:08:28Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 3213228
dc.identifier.wos 000415744000014
dc.identifier.pubmed 28362408
dc.contributor.department SE/AOK/I/OVMBPI/MTA-SE Pathobiokémiai Kutatócsoport
dc.contributor.department SE/AOK/I/Orvosi Vegytani, Molekuláris Biológiai és Patobiokémiai Intézet
dc.contributor.institution Semmelweis Egyetem


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