To further investigate the role of erythropoietin and its receptor in tumor angiogenesis and progression, R3230-GFP cells were engineered to express constitutively active EPOR-R129C, a mutant EPOR that confers growth factor-independent proliferation and tumorigenicity when expressed in immortalized hematopoietic cells but does not transform normal fibroblasts [28]–[31]. This evidence concerns the gene EPOR and neoplasm.