ea hy926 human endothelial cells (ATCC)
Structured Review
![PTUPB decreases DOX-induced sEH and COX-2 expression in human endothelial cells. (A) Basal gene expression levels of sEH and COX-2 in endothelial <t>cells.</t> <t>EA.hy926</t> cells were treated with 0.5 µM, 1 µM and 2 µM DOX for 24H. Gene expression levels of (B) sEH and (C) COX-2 in DOX-treated cells. Viability of EA.hy926 cells treated with either (D) PTUPB alone or (E) in combination with DOX. EA.hy926 cells were treated with 2 µM DOX with or without 1 µM PTUPB for 24 h. Gene expression levels of (F) sEH and (G) COX-2. (H) Activity level of sEH. One-way ANOVA followed by Tukey's multiple comparison tests was performed. + P<0.05 vs. control, *P<0.05 vs. DOX). sEH, soluble epoxide hydrolase; COX-2, cyclooxygenase-2; DOX, doxorubicin; PTUPB, 4-[5-phenyl-3-[3-[[[[4-(trifluoromethyl)phenyl]amino]carbonyl]amino]propyl]-1H-pyrazol-1-yl]-benzenesulfonamide; DHET, dihydroxyeicosatrienoic acid; Con, control.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_9134/pmc12869134/pmc12869134__mmr-33-03-13810-g00.jpg)
Ea Hy926 Human Endothelial Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1807 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 97 stars, based on 1807 article reviews
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1) Product Images from "PTUPB, a soluble epoxide hydrolase/cyclooxygenase-2 dual inhibitor, reduces endothelial-to-mesenchymal transition and improves doxorubicin-induced vascular and cardiac toxicity"
Article Title: PTUPB, a soluble epoxide hydrolase/cyclooxygenase-2 dual inhibitor, reduces endothelial-to-mesenchymal transition and improves doxorubicin-induced vascular and cardiac toxicity
Journal: Molecular Medicine Reports
doi: 10.3892/mmr.2026.13810
Figure Legend Snippet: PTUPB decreases DOX-induced sEH and COX-2 expression in human endothelial cells. (A) Basal gene expression levels of sEH and COX-2 in endothelial cells. EA.hy926 cells were treated with 0.5 µM, 1 µM and 2 µM DOX for 24H. Gene expression levels of (B) sEH and (C) COX-2 in DOX-treated cells. Viability of EA.hy926 cells treated with either (D) PTUPB alone or (E) in combination with DOX. EA.hy926 cells were treated with 2 µM DOX with or without 1 µM PTUPB for 24 h. Gene expression levels of (F) sEH and (G) COX-2. (H) Activity level of sEH. One-way ANOVA followed by Tukey's multiple comparison tests was performed. + P<0.05 vs. control, *P<0.05 vs. DOX). sEH, soluble epoxide hydrolase; COX-2, cyclooxygenase-2; DOX, doxorubicin; PTUPB, 4-[5-phenyl-3-[3-[[[[4-(trifluoromethyl)phenyl]amino]carbonyl]amino]propyl]-1H-pyrazol-1-yl]-benzenesulfonamide; DHET, dihydroxyeicosatrienoic acid; Con, control.
Techniques Used: Expressing, Gene Expression, Activity Assay, Comparison, Control
Figure Legend Snippet: Inhibition of soluble epoxide hydrolase and cyclooxygenase-2 using PTUPB attenuates DOX-induced endothelial-to-mesenchymal transition. EA.hy926 cells were treated with 2 µM DOX with or without 1 µM PTUPB for 24 h. Gene expression levels of mesenchymal markers (A) ASMA, (B) SMA22, (C) VIM, (D) CDH2, (E) TGF-β, (F) SNAI1 and (G) SNAI2, and (H) endothelial marker CD31. (I) Ratio of mesenchymal to endothelial cells in cells treated with DOX with or without 1 µM PTUPB was measured based on morphological images. (J) Representative morphological images of EA.hy926 cells incubated with DOX with or without 1 µM PTUPB for 24 h at a magnification of ×10 (scale bar, 100 µm). The light red arrow indicates mesenchymal cells (long, spindle-like cells). The dark red arrow indicates endothelial cells (cobblestone monolayer-like cells). One-way ANOVA followed by Tukey's multiple comparison test was performed to determine the significant differences between groups ( + P<0.05 vs. control, *P<0.05 vs. DOX). PTUPB, 4-[5-phenyl-3-[3-[[[[4-(trifluoromethyl)phenyl]amino]carbonyl]amino]propyl]-1H-pyrazol-1-yl]-benzenesulfonamide; DOX, doxorubicin; ASMA, smooth muscle actin α2; SMA22, smooth muscle protein 22α; VIM, vimentin; CDH2, cadherin-2; SNAI1, snail family transcriptional repressor 1; SNAI2, snail family transcriptional repressor 2.
Techniques Used: Inhibition, Gene Expression, Marker, Incubation, Comparison, Control