| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-189 |
Sentence |
denotes |
Induction of endothelial cell surface adhesion molecules by tumor necrosis factor is blocked by protein tyrosine phosphatase inhibitors: role of the nuclear transcription factor NF-kappa B. |
| T1 |
0-189 |
Sentence |
denotes |
Induction of endothelial cell surface adhesion molecules by tumor necrosis factor is blocked by protein tyrosine phosphatase inhibitors: role of the nuclear transcription factor NF-kappa B. |
| T2 |
190-466 |
Sentence |
denotes |
Recent studies from our laboratory have indicated that protein tyrosine phosphatase (PTPase) inhibitors can down-modulate the tumor necrosis factor (TNF)-mediated activation of the nuclear transcription factor NF-kappa B in ML-1a, a monocytic cell line (Singh and Aggarwal, J. |
| T2 |
190-466 |
Sentence |
denotes |
Recent studies from our laboratory have indicated that protein tyrosine phosphatase (PTPase) inhibitors can down-modulate the tumor necrosis factor (TNF)-mediated activation of the nuclear transcription factor NF-kappa B in ML-1a, a monocytic cell line (Singh and Aggarwal, J. |
| T3 |
467-472 |
Sentence |
denotes |
Biol. |
| T3 |
467-472 |
Sentence |
denotes |
Biol. |
| T4 |
473-478 |
Sentence |
denotes |
Chem. |
| T4 |
473-478 |
Sentence |
denotes |
Chem. |
| T5 |
479-484 |
Sentence |
denotes |
1995: |
| T5 |
479-484 |
Sentence |
denotes |
1995: |
| T6 |
485-489 |
Sentence |
denotes |
270: |
| T6 |
485-489 |
Sentence |
denotes |
270: |
| T7 |
490-497 |
Sentence |
denotes |
10631). |
| T7 |
490-497 |
Sentence |
denotes |
10631). |
| T8 |
498-878 |
Sentence |
denotes |
Since TNF is one of the major inducers of various adhesion molecules in human endothelial cells and their expression is known to require the activation of NF-kappa B, we examined the effect of PTPase inhibitors on the TNF-mediated induction of intracellular adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1 and endothelial leukocyte adhesion molecule (ELAM)-1. |
| T8 |
498-878 |
Sentence |
denotes |
Since TNF is one of the major inducers of various adhesion molecules in human endothelial cells and their expression is known to require the activation of NF-kappa B, we examined the effect of PTPase inhibitors on the TNF-mediated induction of intracellular adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1 and endothelial leukocyte adhesion molecule (ELAM)-1. |
| T9 |
879-1119 |
Sentence |
denotes |
Like ML-1a, human dermal microvessel endothelial cells (MVEC) treated with TNF rapidly activated (within 30 min) NF-kappa B; this effect was completely abolished by co-treatment with phenylarsine oxide (PAO), a specific inhibitor of PTPase. |
| T9 |
879-1119 |
Sentence |
denotes |
Like ML-1a, human dermal microvessel endothelial cells (MVEC) treated with TNF rapidly activated (within 30 min) NF-kappa B; this effect was completely abolished by co-treatment with phenylarsine oxide (PAO), a specific inhibitor of PTPase. |
| T10 |
1120-1272 |
Sentence |
denotes |
The induction of ICAM-1, VCAM-1, and ELAM-1 by TNF in MVEC occurred within 6 h and was also completely down-regulated by PAO in a dose-dependent manner. |
| T10 |
1120-1272 |
Sentence |
denotes |
The induction of ICAM-1, VCAM-1, and ELAM-1 by TNF in MVEC occurred within 6 h and was also completely down-regulated by PAO in a dose-dependent manner. |
| T11 |
1273-1386 |
Sentence |
denotes |
PAO was found to be effective even when added 3 h after TNF, suggesting a rapid mode of action of this inhibitor. |
| T11 |
1273-1386 |
Sentence |
denotes |
PAO was found to be effective even when added 3 h after TNF, suggesting a rapid mode of action of this inhibitor. |
| T12 |
1387-1561 |
Sentence |
denotes |
Besides PAO, other inhibitors of PTPase, including pervanadate and diamide, also blocked TNF-dependent NF-kappa B activation and induction of all the three adhesion proteins. |
| T12 |
1387-1561 |
Sentence |
denotes |
Besides PAO, other inhibitors of PTPase, including pervanadate and diamide, also blocked TNF-dependent NF-kappa B activation and induction of all the three adhesion proteins. |
| T13 |
1562-1671 |
Sentence |
denotes |
Consistent with these results, the attachment of monocytes to MVEC was also blocked by the PTPase inhibitors. |
| T13 |
1562-1671 |
Sentence |
denotes |
Consistent with these results, the attachment of monocytes to MVEC was also blocked by the PTPase inhibitors. |
| T14 |
1672-1853 |
Sentence |
denotes |
Thus, overall, our results demonstrate that a PTPase is involved either directly or indirectly in the pathway leading to the induction of endothelial cell adhesion molecules by TNF. |
| T14 |
1672-1853 |
Sentence |
denotes |
Thus, overall, our results demonstrate that a PTPase is involved either directly or indirectly in the pathway leading to the induction of endothelial cell adhesion molecules by TNF. |
| T15 |
1854-2015 |
Sentence |
denotes |
Because of their role in cell adhesion, PTPase may provide a novel target of drug development for treatment of inflammation, atherogenesis, and tumor metastasis. |
| T15 |
1854-2015 |
Sentence |
denotes |
Because of their role in cell adhesion, PTPase may provide a novel target of drug development for treatment of inflammation, atherogenesis, and tumor metastasis. |