Source:http://linkedlifedata.com/resource/pubmed/id/21145750
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2011-1-3
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pubmed:abstractText |
This work investigated the in vitro and in vivo anti-angiogenic activity of some pyrroloazaflavones, exactly 2-phenyl-1H-pyrrolo[2,3-h]quinolin-4(7H)ones, with vinblastine as reference compound. Growth inhibitory activity, migration, and capillary-like structures formation were determined in human umbilical vein endothelial cell cultures, and Matrigel plug assay was carried out to evaluate in vivo effects on angiogenesis. Collectively, our results indicate that some pyrroloazaflavone derivatives, at non-cytotoxic concentrations and like vinblastine are able: (i) to exert in vitro anti-angiogenic activity and (ii) to counteract in vitro and in vivo the pro-angiogenic effects of fibroblast growth factor-2 (FGF-2).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1464-3391
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
448-57
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pubmed:meshHeading |
pubmed-meshheading:21145750-Angiogenesis Inhibitors,
pubmed-meshheading:21145750-Animals,
pubmed-meshheading:21145750-Apoptosis,
pubmed-meshheading:21145750-Aza Compounds,
pubmed-meshheading:21145750-Cell Movement,
pubmed-meshheading:21145750-Cells, Cultured,
pubmed-meshheading:21145750-Endothelium, Vascular,
pubmed-meshheading:21145750-Flavones,
pubmed-meshheading:21145750-Humans,
pubmed-meshheading:21145750-Magnetic Resonance Spectroscopy,
pubmed-meshheading:21145750-Mice,
pubmed-meshheading:21145750-Mice, Inbred C57BL,
pubmed-meshheading:21145750-Pyrroles,
pubmed-meshheading:21145750-Spectrometry, Mass, Electrospray Ionization
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pubmed:year |
2011
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pubmed:articleTitle |
Synthesis, in vitro and in vivo preliminary evaluation of anti-angiogenic properties of some pyrroloazaflavones.
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pubmed:affiliation |
Department of Pharmaceutical Sciences, University of Padova, via F. Marzolo, 5, 35131 Padova, Italy. mariagrazia.ferlin@unipd.it
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pubmed:publicationType |
Journal Article
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