<p>(A) Akt phosphorylation induced by IGF-1 and insulin. hTCEpi cells were starved for 24 h in KBM-2 culture medium and then stimulated with IGF-1 (100 ng/ml) or insulin (100 ng/ml) for 15 min. Whole cell lysates were immunoblotted (IB) with anti-phospho-IGF-1Rβ, anti-IGF-1Rβ, anti-INSRβ, anti-phospho-Akt, anti-Akt, or anti-β-actin (loading control) as indicated. (B) IGF-1-induced IGF-1R phosphorylation. Protein lysates obtained as above were immunoprecipitated (IP) with anti-IGF-1Rβ (CST#3027) or anti-INSRβ (C-19) and phosphorylation of both receptors was detected on immunoblots with anti-PY20. Blots are representative of at least two repeated experiments.</p
<p>All IGF-1 stimulation experiments were subject to serum starvation for 24 hours prior to compound...
<p>(A) Hcc193 and A549 cells were treated with NVP-ADW742 (0.1 to 3 µM) for 2 h before 10 min incuba...
Cardiomyocytes were transfected with scrambled (Scr) or PC1 siRNA (siPC1), incubated for 24 h, and t...
<p>(A) Neutralization of IGF-1 receptor and inhibition of IGF-1R/PI3K/Akt pathway. hTCEpi cells were...
<p>(A) Existence of IGF-1R and INSR αβ-dimers after reducing immunoprecipitation. hTCEpi lysates wer...
<p>Serum-depleted 3T3-L1 cells were stimulated with 100 µg/ml AGEs for 15 min, and cell lysates were...
<p><i>A</i>. Flp-In HEK293 cells stably expressing GFP-IRS2 were starved for serum and incubated for...
<p>After 24-h serum starvation wt IGF-1R (A) and K1003R (B) cells were stimulated for indicated time...
<p>A, Wild type and L1361R mutant IGF1R autophosphorylation in transiently transfected R<sup>−</sup>...
<p>A) Late-passage E6/7-HFKs were pre-treated with 10ng/mL IGFBP2 for 1 hour prior to 10 minutes of ...
<p>(A, C & E): The effect of IGF-1R suppression on AKT/PI3K signaling was examined in pancreatic can...
<p>Activation of tyrosine kinase receptors by their ligands stimulates the activity of PI-3 kinase, ...
<p>The activation of Erk (A), Akt (B), and IGF1R/INSR receptors (C) was analyzed by western blotting...
<p>(A,B) Total cell lysates from MDA-MB-435+mock, MDA-MB-435+E-cad and MDA-MB-435+E-cad stimulated (...
<p>(A) hR1, Hex-hR1, but not hRS7 (irrelevant IgG) induced phosphorylation of IGF-1Rβ and Akt in MCF...
<p>All IGF-1 stimulation experiments were subject to serum starvation for 24 hours prior to compound...
<p>(A) Hcc193 and A549 cells were treated with NVP-ADW742 (0.1 to 3 µM) for 2 h before 10 min incuba...
Cardiomyocytes were transfected with scrambled (Scr) or PC1 siRNA (siPC1), incubated for 24 h, and t...
<p>(A) Neutralization of IGF-1 receptor and inhibition of IGF-1R/PI3K/Akt pathway. hTCEpi cells were...
<p>(A) Existence of IGF-1R and INSR αβ-dimers after reducing immunoprecipitation. hTCEpi lysates wer...
<p>Serum-depleted 3T3-L1 cells were stimulated with 100 µg/ml AGEs for 15 min, and cell lysates were...
<p><i>A</i>. Flp-In HEK293 cells stably expressing GFP-IRS2 were starved for serum and incubated for...
<p>After 24-h serum starvation wt IGF-1R (A) and K1003R (B) cells were stimulated for indicated time...
<p>A, Wild type and L1361R mutant IGF1R autophosphorylation in transiently transfected R<sup>−</sup>...
<p>A) Late-passage E6/7-HFKs were pre-treated with 10ng/mL IGFBP2 for 1 hour prior to 10 minutes of ...
<p>(A, C & E): The effect of IGF-1R suppression on AKT/PI3K signaling was examined in pancreatic can...
<p>Activation of tyrosine kinase receptors by their ligands stimulates the activity of PI-3 kinase, ...
<p>The activation of Erk (A), Akt (B), and IGF1R/INSR receptors (C) was analyzed by western blotting...
<p>(A,B) Total cell lysates from MDA-MB-435+mock, MDA-MB-435+E-cad and MDA-MB-435+E-cad stimulated (...
<p>(A) hR1, Hex-hR1, but not hRS7 (irrelevant IgG) induced phosphorylation of IGF-1Rβ and Akt in MCF...
<p>All IGF-1 stimulation experiments were subject to serum starvation for 24 hours prior to compound...
<p>(A) Hcc193 and A549 cells were treated with NVP-ADW742 (0.1 to 3 µM) for 2 h before 10 min incuba...
Cardiomyocytes were transfected with scrambled (Scr) or PC1 siRNA (siPC1), incubated for 24 h, and t...