| Literature DB >> 25308938 |
Ingrid Leguerney1, Jean-Yves Scoazec2, Nicolas Gadot2, Nina Robin3, Frédérique Pénault-Llorca3, Steeve Victorin4, Nathalie Lassau4.
Abstract
Expression levels of endoglin, αv integrin and vascular endothelial growth factor receptor 2 (VEGFR2) were investigated using targeted, contrast-enhanced ultrasonography in murine melanoma tumor models. Microvasculature and expression levels of biomarkers were investigated using specific contrast agents conjugated with biotinylated monoclonal antibodies. Ultrasound signal intensity from bound contrast agents was evaluated in two groups of mice: control mice and mice treated with sorafenib. Expression levels were analyzed by immunohistochemistry. Endoglin biomarkers were more highly expressed than αv integrin and VEGFR2. Endoglin decreased in the sorafenib group, whereas it tended to increase with time in the control group. Targeted ultrasound contrast agents may be used for non-invasive longitudinal evaluation of tumor angiogenesis during tumor growth or therapeutic treatment in preclinical studies. Endoglin protein, which plays an important role in angiogenesis, seems to be a target of interest for detection of cancer and for prediction of therapeutic efficacy.Entities:
Keywords: Endoglin; Integrin; Molecular imaging; Targeted ultrasound contrast agents; Vascular endothelial growth factor receptor 2
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Year: 2014 PMID: 25308938 DOI: 10.1016/j.ultrasmedbio.2014.06.014
Source DB: PubMed Journal: Ultrasound Med Biol ISSN: 0301-5629 Impact factor: 2.998