“…9,10,29 Clinical studies demonstrated upregulated levels of VEGF and its receptors VEGFR1-R3, particularly in human angiosarcomas. 9 Therefore, to genetically determine the role of autocrine VEGF sources in endothelial and hematopoietic-related tumorigenesis in vivo, we generated Tie2-Cre, p53 fl/fl , VEGF fl/+ and Tie2-Cre, p53 fl/fl , VEGF fl/fl mice to conditionally delete either one or both VEGF alleles, respectively.…”