Inhibition of vascular endothelial growth factor-induced endothelial cell migration by ETS1 antisense oligonucleotides

Z Chen, RJ Fisher, CW Riggs, JS Rhim… - Cancer research, 1997 - AACR
Z Chen, RJ Fisher, CW Riggs, JS Rhim, JA Lautenberger
Cancer research, 1997AACR
Vascular endothelial growth factor (VEGF) increased the level of ETS1 mRNA in human
umbilical vein endothelial cells (HUVEC) and human lung microvascular endothelial cells
(HMVEC-L) over 5-fold. Protein levels were shown to increase concordantly. VEGF was also
found to stimulate the invasiveness of endothelial cells as measured by migration through
Matrigel-or gelatin-coated membranes. The VEGF-induced invasiveness was inhibited by
ETS1 antisense oligonucleotides but not by a sense control. In addition, the ETS1 antisense …
Abstract
Vascular endothelial growth factor (VEGF) increased the level of ETS1 mRNA in human umbilical vein endothelial cells (HUVEC) and human lung microvascular endothelial cells (HMVEC-L) over 5-fold. Protein levels were shown to increase concordantly. VEGF was also found to stimulate the invasiveness of endothelial cells as measured by migration through Matrigel- or gelatin-coated membranes. The VEGF-induced invasiveness was inhibited by ETS1 antisense oligonucleotides but not by a sense control. In addition, the ETS1 antisense oligonucleotides reduced the levels of ETS1 and urokinase-type plasminogen activator mRNAs. The antisense oligonucleotides directed against the ETS1 gene thus altered a cellular property of endothelial cells that is correlated with the ability of the cells to migrate through basement membranes. Together, these observations demonstrate a direct role for the ETS1 gene in angiogenesis.
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