Research Article

PBX3 Promotes Tumor Growth and Angiogenesis via Activation of AT1R/VEGFR2 Pathway in Papillary Thyroid Carcinoma

Figure 3

PBX3 promoted PTC cell proliferation and angiogenesis via activation of AT1R/VEGFR2 pathway. (a) Overexpression of ATRAP, knockdown of AT1R or cabozantinib treatment inhibited PTC cell proliferation, (b) inhibited VEGF production in cell culture, and (c) induced downregulation of VEGFR2 and its downstream (p-ERK1/2, p-AKT and p-Src). (d) AT1R overexpression and VEGFA administration rescued shRNA-PBX3-inhibited phosphorylation of VEGFR2. (e) The tube branch points of HUVECs (magnification, ×10) and angiogenesis of chick chorioallantoic membrane (magnification, ×10) induced by tumor conditioned medium treated with LV-PBX3, shRNA-PBX3, LV-ATRAP, shRNA-AT1R or cabozantinib. All values are shown as mean ± SD. versus control group.
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