4.6 Article

Thio-Cl-IB-MECA, a novel A3 adenosine receptor agonist, suppresses angiogenesis by regulating PI3K/AKT/mTOR and ERK signaling in endothelial cells

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出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2013.06.040

关键词

Thio-Cl-IB-MECA; Anti-angiogenesis; PI3K/AKT/mTOR; ERK; Endothelial cells

资金

  1. National Research Foundation
  2. Korean Government (MEST) [2009-0083533]
  3. Seoul RBD program [10541]

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Although A(3)AR agonists exhibit a variety of biological activities including anticancer effects, their possible anti-angiogenic effects have not yet been investigated. In the present study, we assayed the anti-angiogenic activity of thio-Cl-IB-MECA, a novel A(3)AR agonist, in cultured HUVECs and mES/EB-derived endothelial cells. Thio-Cl-IB-MECA inhibited migration and tube formation by endothelial cells and dramatically decreased ex vivo microvessel sprouting in cultured mouse aortic rings. The anti-angiogenic activity of thio-Cl-IB-MECA was associated with suppression of the expression of the endothelial biomarker PECAM via regulation of PI3K/AKT/mTOR and ERIK signaling in mES/EB-derived endothelial cells. (c) 2013 Elsevier Inc. All rights reserved.

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