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. 2013 Jan 5;3(1):16–31.

Figure 3.

Figure 3

Intratumoral administration of EGFR antisense plasmid DNA has antitumor efficacy. One million SCCHN cells (1483) were injected subcutaneously into six athymic nude mice on both flanks. EGFR sense plasmid DNA (■) or antisense plasmid DNA (▲) (25 μg/tumor) was administered daily into the left and right tumor respectively. Tumors were measured twice a week. The graph depicts growth of the tumors over the treatment period. B: EGFR antisense gene therapy reduces SCCHN xenograft cell proliferation. SCCHN tumors treated with either EGFR antisense or sense gene therapy were paraffin-embedded and examined for proliferation using Ki-67 staining. Positive cells demonstrated by the dark brown nuclear staining were counted under 400X magnification in 10 separate fields. There was a significant difference between tumors treated with EGFR antisense oligonucleotides compared to the control (p= 0.0001). Error bars indicate ± SEM.