EGFR-Mutant Lung Tumors Lacking the RAS-PI3K Interaction Show Strongly Delayed Development
(A) Volume of air remaining in mouse lungs after tamoxifen (2 weeks) and doxycycline diet at different time points (n = 26 for Pik3caWT/− and n = 21 for Pik3caMUT/−).
(B) Representative examples of lungs visualized by micro-CT scan (left), ex-vivo view (middle), and histological sections stained with H&E after 18 weeks of a doxycycline diet.
(C) Quantification of the number of tumor foci per lung after 18 weeks of a doxycycline diet from histological samples (n = 7 per group).
(D) Quantification of the area of the lung occupied by tumor foci after 18 weeks of a doxycycline diet from histological samples (n = 7 per group).
(E) Representative examples of proliferation in tumor samples visualized by Ki-67 staining. Scale bar, 100 μm.
(F) Quantification of proliferation by Ki-67 staining (n = 6 per group).
(G) Survival assay. The endpoint was dictated by defined welfare severity limits: moderately increased respiratory rate and/or moderately hunched appearance (n = 11 for Pik3caWT/Flox, n = 11 for Pik3caWT/−, and n = 15 for Pik3caMUT/−).