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. 2013 Nov 11;24(5):617–630. doi: 10.1016/j.ccr.2013.09.012

Figure 2.

Figure 2

Expression of p110α-RBD in Established Tumors Reduces Tumor Burden

(A) Schematic representation of mouse treatment and micro-CT scanning intervals.

(B) Ten-week-old mice were left untreated or were treated with tamoxifen for 2 weeks and the effect on tumor volume was assessed by micro-CT analysis over a 6-week period. Tumor volumes are plotted relative to the initial volume at the start of treatment. Black lines represent tumors from Pik3caWT/− mice and red lines represent tumors from Pik3caRBD/− mice. Green lines represent tumors from tamoxifen-treated Pik3caWT/WT mice that express Cre recombinase following treatment but do not have loxP sites flanking the Pik3ca gene. Pik3caWT/flox n = 4 mice, Pik3caRBD/flox n = 4, Pik3caWT/- n = 6, Pik3caRBD/- n = 4, Pik3caWT/WT n = 3 mice.

(C) Quantification of TUNEL-positive tumors following tamoxifen treatment for 11 days. Pik3caWT/− n = 5 mice, Pik3caRBD/− n = 7 mice

(D) Quantification of tumor multiplicity on the pleural surface of lungs. Representative images of lungs from Pik3caWT/flox, Pik3caRBD/flox, Pik3caWT/−, and Pik3caRBD/− mice at 16 weeks of age are shown.

(E) Quantification of tumor burden (tumor area as a percentage of total lung area) in mice 6 weeks after commencement of tamoxifen treatment. Representative images of histological sections stained with H&E in Pik3caWT/flox, Pik3caRBD/flox, Pik3caWT/−, and Pik3caRBD/− mice at 16 weeks of age are shown.

Error bars indicate mean ± SEM (significance using Student’s t test: p < 0.05 ∗∗p < 0.01). See also Figure S2.