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  • Antiangiogenic activity of the brassinosteroid plant hormones (BRs) and their derivative cholestanon was investigated in human umbilical vein endothelial cells (HUVEC) and in human microvascular endothelial cells (HMEC-1). 24-Epibrassinolide and 28-homocastasterone from group of 21 tested natural BRs inhibited migration of HUVEC cells. Seven tested BRs decreased the number of tubes significantly. Synthetic analogue cholestanon inhibited angiogenesis in vitro more effectively than natural BRs. Because of the similarity of BRs to human steroids, we have also studied interactions of BRs with human steroid receptors. Synthetic BRs cholestanon showed agonistic effects on estrogen-receptor-alpha, estrogen-receptor-beta and androgen receptor. Of the natural BRs, 24-epibrassinolide was found to be a weak antagonist of estrogen-receptor-alpha (ER alpha). Our results provide the first evidence that large group of BRs can inhibit in vitro angiogenesis of primary endothelial cells. BRs constitute a novel group of human steroid receptor activators or inhibitors with capacity to inhibit angiogenesis.
  • Antiangiogenic activity of the brassinosteroid plant hormones (BRs) and their derivative cholestanon was investigated in human umbilical vein endothelial cells (HUVEC) and in human microvascular endothelial cells (HMEC-1). 24-Epibrassinolide and 28-homocastasterone from group of 21 tested natural BRs inhibited migration of HUVEC cells. Seven tested BRs decreased the number of tubes significantly. Synthetic analogue cholestanon inhibited angiogenesis in vitro more effectively than natural BRs. Because of the similarity of BRs to human steroids, we have also studied interactions of BRs with human steroid receptors. Synthetic BRs cholestanon showed agonistic effects on estrogen-receptor-alpha, estrogen-receptor-beta and androgen receptor. Of the natural BRs, 24-epibrassinolide was found to be a weak antagonist of estrogen-receptor-alpha (ER alpha). Our results provide the first evidence that large group of BRs can inhibit in vitro angiogenesis of primary endothelial cells. BRs constitute a novel group of human steroid receptor activators or inhibitors with capacity to inhibit angiogenesis. (en)
Title
  • Brassinosteroids inhibit in vitro angiogenesis in human endothelial cells
  • Brassinosteroids inhibit in vitro angiogenesis in human endothelial cells (en)
skos:prefLabel
  • Brassinosteroids inhibit in vitro angiogenesis in human endothelial cells
  • Brassinosteroids inhibit in vitro angiogenesis in human endothelial cells (en)
skos:notation
  • RIV/61989592:15310/12:33142882!RIV13-MSM-15310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(ED0007/01/01), P(GA301/08/1649), P(LC06077), Z(AV0Z40550506), Z(AV0Z50380511), Z(AV0Z50520514)
http://linked.open...iv/cisloPeriodika
  • 13
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 125487
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15310/12:33142882
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Receptors; Natural products; Migration; Human umbilical vein endothelial cells; Angiogenesis (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [B81B16C6C95D]
http://linked.open...i/riv/nazevZdroje
  • Steroids
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 77
http://linked.open...iv/tvurceVysledku
  • Bartůněk, Petr
  • Kohout, Ladislav
  • Kryštof, Vladimír
  • Strnad, Miroslav
  • Rárová, Lucie
  • Sedlák, David
  • Liebl, Johanna
  • Zahler, Stefan
http://linked.open...ain/vavai/riv/wos
  • 000312423300024
http://linked.open...n/vavai/riv/zamer
issn
  • 0039-128X
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.steroids.2012.08.011
http://localhost/t...ganizacniJednotka
  • 15310
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