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. Author manuscript; available in PMC: 2016 Sep 1.
Published in final edited form as: Cancer Res. 2015 Jul 2;75(17):3492–3504. doi: 10.1158/0008-5472.CAN-15-0088

Figure 3. Tumor angiogenesis is increased in AIP1-ecKO mice.

Figure 3

Mouse breast cancer cells (1×106) were injected orthotopically into the fourth mammary gland of WT and AIP1-ecKO mice, and tumor along with surrounding mammary tissue were harvested at 2 weeks. AB. Tumor angiogenesis was determined by immunohistochemistry and whole-mount staining with anti-CD31, and intratumoral vessel density and vessel areas were quantified from 5 sections per tumor and n=10 mice for each strain, *, p<0.05. Scale bar: 50 μm. CD. Tumor-induced angiogenesis in lymph nodes was determined by immunostaining with anti-CD31. Scale bar: 100 μm. CD31+ areas were quantified. n=10 mice per group. **, p<0.01. E–G. Phospho-VEGFR2 (pY1054/1059) and total VEGFR2, VEGFR3, AIP1 and β-actin proteins in tumor (E) and lymph node (F–G) were determined by immunoblotting with respective antibodies. Representative blots are shown from 1 of 4 mice for each strain with fold changes compared to WT-tumor are indicated below the blots. Further quantifications of VEGFR2 and p-VEGFR2 are shown in G, n=6 mice per group. **, p<0.01.