ANG-2 and PIGF survival analysis on breast cancer patients | 7C-E), suggesting that the synergistic effect of the corresponding pathways is required to have a significant impact on the survival. |
Discussion | Furthermore, this study demonstrates that the synergistic effect of these treatments relies on crosstalk between TNF-Rl, VEGFR-l, TGF-B and TIE-2 pathways resulting in altered angiogenic activity (Figs. |
Discussion | Moreover, the relapse free survival analysis showed a clear separation between patients with low and high expression for pro-angiogenic genes (ANG-2 and PIGF), and suggested that the synergistic effect of the corresponding pathways is required to have a significant impact on the survival. |
Identification of critical ligands impacting the phenotype and pro-angiogenic activity of TEM differentiated in vitro—Antagonistic effect of TG F-B and synergistic effects of TN F-or on TEM pro-angiogenic phenotype and function | Identification of critical ligands impacting the phenotype and pro-angiogenic activity of TEM differentiated in vitro—Antagonistic effect of TG F-B and synergistic effects of TN For on TEM pro-angiogenic phenotype and function |
The plasticity of TEM predicted computationally was validated experimentally using TEM differentiated in vitro | These results validate our in silico prediction and reveal the synergistic effect of TIE-2, VEGFR-l and TNF-oc pathways in controlling TEM pro-angiogenic activity. |