Linked Life Data

17270026

Source:http://linkedlifedata.com/resource/pubmed/id/17270026

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2007-2-2
pubmed:abstractText
CD13/aminopeptidase-N (CD13/APN) is an important regulator of angiogenesis where its expression on activated blood vessels is induced by angiogenic signals. A previous study demonstrated that angiogenesis is suppressed under the presence of high concentrations of aminopeptidase antagonists. However, the mechanisms underlying the inhibition of morphogenesis by aminopeptidase antagonists have not been elucidated. In this study, we have for the first time examined the effects of continuous treatment of therapeutic dose of aminopeptidase antagonists on vascular endothelial capillary-like tube formation. In the antagonists tested, only bestatin significantly interfered in the capillary tube formation of primary endothelial cells (EC) after treatment for 72 h. Aminopeptidase analysis revealed that inhibitory activity of bestatin was not specific for CD13/APN, and the other inhibitors lacking anti-angiogenic properties also inhibit cell-surface aminopeptidase activity as well or more potently than bestatin, suggesting that the angiogenesis-inhibitory effect of bestatin was not due to inhibition of CD13/APN activity at this concentration. To elucidate the influence of continuous treatment of bestatin on endothelial cells, we performed microarray analysis and revealed that 72-h treatment of a pharmacokinetic dose of bestatin modulated the several angiogenesis-related genes including vascular endothelial growth factor (VEGF). Northern blot analysis indicated that modulation of the VEGF gene became obvious after 48 h of treatment. Furthermore, knockdown of the VEGF gene by siRNA remarkably suppressed capillary tube formation and required a higher concentration of exogenous VEGF to reverse the capillary formation ability. These data suggested that bestatin decreases a reactivity of EC to angiogenesis stimuli, and it can be achieved by the regulation of angiogenesis-related gene expression.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1347-9032
pubmed:author
pubmed:issnType
Print
pubmed:volume
98
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
364-72
pubmed:meshHeading
pubmed-meshheading:17270026-Aminopeptidases, pubmed-meshheading:17270026-Angiogenesis Inducing Agents, pubmed-meshheading:17270026-Capillaries, pubmed-meshheading:17270026-Cell Line, pubmed-meshheading:17270026-Cell Proliferation, pubmed-meshheading:17270026-Coculture Techniques, pubmed-meshheading:17270026-Endothelium, Vascular, pubmed-meshheading:17270026-Fibroblasts, pubmed-meshheading:17270026-Gene Expression Regulation, pubmed-meshheading:17270026-Humans, pubmed-meshheading:17270026-Infant, Newborn, pubmed-meshheading:17270026-Leucine, pubmed-meshheading:17270026-Neovascularization, Physiologic, pubmed-meshheading:17270026-Oligonucleotide Array Sequence Analysis, pubmed-meshheading:17270026-Skin, pubmed-meshheading:17270026-Time Factors, pubmed-meshheading:17270026-Umbilical Veins, pubmed-meshheading:17270026-Vascular Endothelial Growth Factor A
pubmed:year
2007
pubmed:articleTitle
Continuous treatment of bestatin induces anti-angiogenic property in endothelial cells.
pubmed:affiliation
Cancer Chemotherapy Center, Clinical Chemotherapy, Japanese Foundation for Cancer Research, 3-10-6, Ariake, Koto-ku, Tokyo, 135-8550, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't