<?xml version="1.0"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dk.um.si/IzpisGradiva.php?id=65318"><dc:title>The influence of royal jelly and human interferon-alpha (HuIFN-[alpha]N3) on proliferation, glutathione level and lipid peroxidation in human colorectal adenocarcinoma cells in vitro</dc:title><dc:creator>Filipič,	Bratko	(Avtor)
	</dc:creator><dc:creator>Gradišnik,	Lidija	(Avtor)
	</dc:creator><dc:creator>Rihar,	Klemen	(Avtor)
	</dc:creator><dc:creator>Šooš,	Eugen	(Avtor)
	</dc:creator><dc:creator>Pereyra Gonzales,	Adriana	(Avtor)
	</dc:creator><dc:creator>Potokar,	Jana	(Avtor)
	</dc:creator><dc:subject>antiproliferative activity</dc:subject><dc:subject>antitumour activity</dc:subject><dc:subject>malondialddehyde</dc:subject><dc:subject>CaCo-2 cells</dc:subject><dc:subject>10-hydroxy-2-decenoic acid</dc:subject><dc:description>Among royal jelly’s (RJ) various biological activities, its possible antitumour activity deserves particular attention. The purpose of this study was to investigate the influence of RJ, its bioactive component 10-hydroxy-2-decenoic acid (10- HDA), and human interferon-alpha (HuIFN-αN3) on the proliferation of human colorectal adenocarcinoma cells (CaCo- 2), and ascertain their effect on intracellular glutathione (GSH) level and lipid peroxidation. We studied the antiproliferative (AP) activity of RJ [(0.1 g/10 mL phosphate buffer saline (PBS)], HuIFN-αN3 (1000 I.U. mL-1), 10-HDA at 100.0 μmol L-1, and their different combinations, in the ratio 1:1, 1:2, and 2:1 on CaCo-2 cells. The GSH level was measured by glutathione assay. The lipid peroxidation was measured by malondialdehyde (MDA) assay. Single RJ had a low AP activity: 2.0 (0.5 mg mL-1). HuIFN-αN3 had an AP activity of 2.5 (208.33 I.U. mL-1), while 10-HDA had an AP activity of 1.5 (37.5 μmol mL-1). The highest AP activity of 3.8 was obtained when RJ and HuIFN-αN3 were applied at the ratio 2:1. In that combination the level of GSH was 24.9±2.4 nmol g-3 of proteins (vs. 70.2±3.2 nmol g-3 in the control) and the level of MDA was 72.3±3.1 nmol g-3 (vs. 23.6±9.1 nmol g-3 in the control). It is generally assumed that 10-HDA, an important constituent of RJ, together with HuIFN-αN3, is responsible for the inhibition of CaCo-2 cells proliferation in vitro. In our study, however, RJ and HuIFN-αN3 applied at 2:1 decreased the level of GSH the most and significantly increased lipid peroxidation via MDA in CaCo-2 cells. Future studies should show whether these GSH- and MDA-related activities of RJ, HuIFN-αN3, 10-HDA, and their combinations may decrease the tumorigenicity index and tumorigenic potential of various tumour cells in vitro.</dc:description><dc:date>2015</dc:date><dc:date>2017-03-30 15:05:04</dc:date><dc:type>Znanstveno delo</dc:type><dc:identifier>65318</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
