Structural Insight into the In Vitro Anti-Intravasative Properties of Flavonoids

We investigated the effect of 21 flavonoids in a three-dimensional in vitro system for their ability to inhibit gap formation by MCF-7 breast cancer spheroids in monolayers of lymphendothelial cells. Different representatives of the classes of flavones, flavonols, and flavanones were tested in the c...

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Главные авторы: Julia Eichsteininger (Автор), Kerstin Kirisits (Автор), Claudia Smöch (Автор), Christa Stadlbauer (Автор), Chi Huu Nguyen (Автор), Walter Jäger (Автор), Ali Özmen (Автор), Gerhard Ecker (Автор), Georg Krupitza (Автор), Liselotte Krenn (Автор)
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Опубликовано: MDPI AG, 2019-09-01T00:00:00Z.
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100 1 0 |a Julia Eichsteininger  |e author 
700 1 0 |a Kerstin Kirisits  |e author 
700 1 0 |a Claudia Smöch  |e author 
700 1 0 |a Christa Stadlbauer  |e author 
700 1 0 |a Chi Huu Nguyen  |e author 
700 1 0 |a Walter Jäger  |e author 
700 1 0 |a Ali Özmen  |e author 
700 1 0 |a Gerhard Ecker  |e author 
700 1 0 |a Georg Krupitza  |e author 
700 1 0 |a Liselotte Krenn  |e author 
245 0 0 |a Structural Insight into the In Vitro Anti-Intravasative Properties of Flavonoids 
260 |b MDPI AG,   |c 2019-09-01T00:00:00Z. 
500 |a 2218-0532 
500 |a 10.3390/scipharm87030023 
520 |a We investigated the effect of 21 flavonoids in a three-dimensional in vitro system for their ability to inhibit gap formation by MCF-7 breast cancer spheroids in monolayers of lymphendothelial cells. Different representatives of the classes of flavones, flavonols, and flavanones were tested in the circular chemorepellent-induced defects (CCID)-assay. Bay11-7082, a known inhibitor of CCID formation served as the positive control. This study provides the first comparison of the potential of flavonoids to suppress features influencing the intravasation of MCF-7 breast cancer cells aggregates through the lymph endothelial barrier. The most significant effects were seen after incubation with the flavones luteolin, chrysin, and apigenin. Additional hydroxylation or methoxylation in positions 6 or 8, as expected, resulted in decreased activity. The tested flavanones remained without or low efficacy. 
546 |a EN 
690 |a CCID assay 
690 |a inhibition of gap formation 
690 |a flavonoids 
690 |a anti-invasive 
690 |a breast cancer 
690 |a structure-activity relationship 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Scientia Pharmaceutica, Vol 87, Iss 3, p 23 (2019) 
787 0 |n https://www.mdpi.com/2218-0532/87/3/23 
787 0 |n https://doaj.org/toc/2218-0532 
856 4 1 |u https://doaj.org/article/9a52568d42d440f4882d85e1b7f9bca9  |z Connect to this object online.