<p>(A) U87MG cells were treated with or without JSI-124 for 8 hours and then incubated with fresh media without JSI-124 for 24 hours, followed by the collection of conditioned media (CM). (B) VEGF level was analyzed in the conditioned medium by ELISA.</p
<p>A) The dose response used to determine the optimal concentration IP-10p (10 µM) used to compare t...
<p><b>(A)</b> The tube length (arrows) of HMEC-1 cells was increased in CM derived from Ad-GPR4-FaDu...
<p>(A) and (B), HUVEC tubule formation <i>in vitro</i> in the Matrigel after 12 hours co-culture wit...
<p>Cells were exposed to different doses of JSI-124 for 24 hours and VEGF protein released by GBM ce...
<p>(A) Effect of JSI-124 on VEGF-induced HUVECs proliferation determined by CCK-8 assay. HUVECs (5×1...
<p>(A) JSI-124 suppressed the activation of VEGFR2 induced by VEGF in HUVECs in a dose-dependent man...
<p>U87MG cells were cultured in the well (lower chamber). Cells were then treated with or without JS...
<p>(A) Effect of JSI-124 on HUVECs under normal culture condition. HUVECs (5×10<sup>3</sup>/ well) w...
<div><p>Glioblastoma multiforme (GBM) is one of the utmost malignant tumors. Excessive angiogenesis ...
<p>HUVEC were grown under 0.5% serum conditions and treated with or without VEGF (10 ng/mL) and vari...
<p>Serum-starved HUVECs were stimulated with VEGF (30 ng/mL) in the presence or absence of <b>1</b> ...
<p>(a) Luteolin inhibited HUVECs migration. Cells were starved to inactivate cell proliferation and ...
<p>Tube formation assay: (A) control-siRNA H1975 cells; (B) RBP2-siRNA1 H1975 cells; (C) RBP2-siRNA2...
<p>Effect of JSI-124 at 100 nM on GBM cells invasiveness performed by transwell invasion analysis. A...
<p>143B cells were transduced with lentiviruses expressing either scrambled (shCtrl) or α-CaMKII- ta...
<p>A) The dose response used to determine the optimal concentration IP-10p (10 µM) used to compare t...
<p><b>(A)</b> The tube length (arrows) of HMEC-1 cells was increased in CM derived from Ad-GPR4-FaDu...
<p>(A) and (B), HUVEC tubule formation <i>in vitro</i> in the Matrigel after 12 hours co-culture wit...
<p>Cells were exposed to different doses of JSI-124 for 24 hours and VEGF protein released by GBM ce...
<p>(A) Effect of JSI-124 on VEGF-induced HUVECs proliferation determined by CCK-8 assay. HUVECs (5×1...
<p>(A) JSI-124 suppressed the activation of VEGFR2 induced by VEGF in HUVECs in a dose-dependent man...
<p>U87MG cells were cultured in the well (lower chamber). Cells were then treated with or without JS...
<p>(A) Effect of JSI-124 on HUVECs under normal culture condition. HUVECs (5×10<sup>3</sup>/ well) w...
<div><p>Glioblastoma multiforme (GBM) is one of the utmost malignant tumors. Excessive angiogenesis ...
<p>HUVEC were grown under 0.5% serum conditions and treated with or without VEGF (10 ng/mL) and vari...
<p>Serum-starved HUVECs were stimulated with VEGF (30 ng/mL) in the presence or absence of <b>1</b> ...
<p>(a) Luteolin inhibited HUVECs migration. Cells were starved to inactivate cell proliferation and ...
<p>Tube formation assay: (A) control-siRNA H1975 cells; (B) RBP2-siRNA1 H1975 cells; (C) RBP2-siRNA2...
<p>Effect of JSI-124 at 100 nM on GBM cells invasiveness performed by transwell invasion analysis. A...
<p>143B cells were transduced with lentiviruses expressing either scrambled (shCtrl) or α-CaMKII- ta...
<p>A) The dose response used to determine the optimal concentration IP-10p (10 µM) used to compare t...
<p><b>(A)</b> The tube length (arrows) of HMEC-1 cells was increased in CM derived from Ad-GPR4-FaDu...
<p>(A) and (B), HUVEC tubule formation <i>in vitro</i> in the Matrigel after 12 hours co-culture wit...
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