Complement activation plays a critical role in controlling inflammatory responses. To assess the role of complement during ovarian cancer progression, we crossed two strains of mice with genetic complement deficiencies with transgenic mice that develop epithelial ovarian cancer (TgMISIIR-TAg). TgMISIIR-TAg mice fully or partially deficient for complement factor 3 (C3) (Tg⁺C3^KO and Tg⁺C3^HET, respectively) or fully deficient for complement factor C5a receptor (C5aR) (Tg⁺C5aR^KO) develop either no ovarian tumors or tumors that were small and poorly vascularized compared to wild-type littermates (Tg⁺C3^WT, Tg⁺C5aR^WT). The percentage of tumor infiltrating immune cells in Tg⁺C3^HET tumors compared to Tg⁺C3^WT controls was either similar (macrophages, B cells, myeloid-derived suppressor cells), elevated (effector T cells), or decreased (regulatory T cells). Regardless of these ratios, cytokine production by immune cells taken from Tg⁺C3^HET tumors was reduced on stimulation compared to Tg⁺C3^WT controls. Interestingly, CD31⁺ endothelial cell (EC) function in angiogenesis was significantly impaired in both C3^KO and C5aR^KO mice. Further, using the C5aR antagonist PMX53, tube formation of ECs was shown to be C5a-dependent, possibly through interactions with the VEGF₁₆₅ but not VEGF₁₂₁ isoform. Finally, the mouse VEGF₁₆₄ transcript was underexpressed in C3^KO livers compare to C3^WT livers. Thus, we conclude that complement inhibition blocks tumor outgrowth by altering EC function and VEGF₁₆₅ expression.