<p>A. Membrane localization of β-catenin decreased while nuclear/perinuclear β-catenin (white arrows) increased in TGF-β1-treated cells compared to untreated (vehicle) controls. Concurrent treatment with both TGF-β1 and troglitazone maintained β-catenin at the cell plasma membrane and prevented β-catenin nuclear translocation. Nuclei are labeled with propidium iodide. <i>*P</i><0.05 compared to TGF-β1; n = 3. B. Following concomitant treatment with LiCl (7.5 mM), troglitazone and TGF-β1 (2.5 ng/ml), LiCl prevented inhibition of TGF-β1-mediated α-SMA expression by troglitazone. <i>*P</i><0.05 compared to vehicle; <i>**P</i><0.05 compared to vehicle in the presence of TGF-β1 and troglitazone; n = 4. C. SNAI1 activity was increased upon stimul...
Troglitazone is a synthetic ligand of peroxisome proliferators activated receptor-gamma (PPAR gamma)...
<p>A) I.F. microscopy was performed on DU145 prostate tumor cells expressing either a non-target (sc...
TGF-beta activation has been inhibited with Troglitazone, a synthetic PPARgamma ligand (Peng, Liu et...
<p>A. Under control conditions, cells exhibit cobblestone appearance typical of epithelial morpholog...
<p>A. Following treatment with TGF-β1 for 1 h, primary AEC exhibit marked phosphorylation of Akt at ...
<p>Western analysis reveals inhibition of TGF-β1-mediated decreases in ZO-1 (A) and increases in α-S...
Peroxisome proliferator activated receptor γ (PPARγ) agonists are effective antifibrotic agents in a...
<div><p>Peroxisome proliferator activated receptor γ (PPARγ) agonists are effective antifibrotic age...
Peroxisome proliferator activated receptor c (PPARc) agonists are effective antifibrotic agents in a...
<p><b>Copyright information:</b></p><p>Taken from "Troglitazone suppresses transforming growth facto...
Troglitazone, an agonist of peroxisome proliferator activated receptorγ (PPARγ), has been reported t...
Abstract Background Troglitazone (TGZ) is a potential anticancer agent. Little is known about the ef...
<p>(A) The extent of mAb SAM-1 (anti-α5) binding to K562 cells exposed to vehicle, 9-<i>cis</i>-RA, ...
<p>A) DU145 prostate tumor cells were treated with 10 µM Troglitazone and/or HGF overnight, followed...
<p>Oral carcinoma cells (TSU, KOSC2, HSC2, SCCKN) and HaCaT cells were treated with TGF-β (lane b), ...
Troglitazone is a synthetic ligand of peroxisome proliferators activated receptor-gamma (PPAR gamma)...
<p>A) I.F. microscopy was performed on DU145 prostate tumor cells expressing either a non-target (sc...
TGF-beta activation has been inhibited with Troglitazone, a synthetic PPARgamma ligand (Peng, Liu et...
<p>A. Under control conditions, cells exhibit cobblestone appearance typical of epithelial morpholog...
<p>A. Following treatment with TGF-β1 for 1 h, primary AEC exhibit marked phosphorylation of Akt at ...
<p>Western analysis reveals inhibition of TGF-β1-mediated decreases in ZO-1 (A) and increases in α-S...
Peroxisome proliferator activated receptor γ (PPARγ) agonists are effective antifibrotic agents in a...
<div><p>Peroxisome proliferator activated receptor γ (PPARγ) agonists are effective antifibrotic age...
Peroxisome proliferator activated receptor c (PPARc) agonists are effective antifibrotic agents in a...
<p><b>Copyright information:</b></p><p>Taken from "Troglitazone suppresses transforming growth facto...
Troglitazone, an agonist of peroxisome proliferator activated receptorγ (PPARγ), has been reported t...
Abstract Background Troglitazone (TGZ) is a potential anticancer agent. Little is known about the ef...
<p>(A) The extent of mAb SAM-1 (anti-α5) binding to K562 cells exposed to vehicle, 9-<i>cis</i>-RA, ...
<p>A) DU145 prostate tumor cells were treated with 10 µM Troglitazone and/or HGF overnight, followed...
<p>Oral carcinoma cells (TSU, KOSC2, HSC2, SCCKN) and HaCaT cells were treated with TGF-β (lane b), ...
Troglitazone is a synthetic ligand of peroxisome proliferators activated receptor-gamma (PPAR gamma)...
<p>A) I.F. microscopy was performed on DU145 prostate tumor cells expressing either a non-target (sc...
TGF-beta activation has been inhibited with Troglitazone, a synthetic PPARgamma ligand (Peng, Liu et...