Fig. 2.
Fig. 2. Demonstration of the ability of AdNK4 to inhibit tumor vascularization. / For immunohistochemical evaluations for CD31, BALB/c mice were injected subcutaneously in the right flank with 2 × 105 Colon-26 cells (day 0). On day 8, tumor-bearing mice were treated by intratumoral injection of 109 pfu of AdNK4 (A), AdNull (B), or PBS alone (no transduction, C). On day 11, tumors were dissected, and frozen tumor sections were stained using 12.5 μg/mL rat anti–mouse CD31 antibody, or isotype-matched control rat IgG followed by visualization with FITC-conjugated anti–rat IgG antibody. Nuclei were stained with DAPI (original magnification × 400). The number of CD31+ vessels per 10 random high-power fields is indicated in the lower right corner of each left panel.

Demonstration of the ability of AdNK4 to inhibit tumor vascularization.

For immunohistochemical evaluations for CD31, BALB/c mice were injected subcutaneously in the right flank with 2 × 105 Colon-26 cells (day 0). On day 8, tumor-bearing mice were treated by intratumoral injection of 109 pfu of AdNK4 (A), AdNull (B), or PBS alone (no transduction, C). On day 11, tumors were dissected, and frozen tumor sections were stained using 12.5 μg/mL rat anti–mouse CD31 antibody, or isotype-matched control rat IgG followed by visualization with FITC-conjugated anti–rat IgG antibody. Nuclei were stained with DAPI (original magnification × 400). The number of CD31+ vessels per 10 random high-power fields is indicated in the lower right corner of each left panel.

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