Skip to main content
. 2023 Jan 25;15(3):737. doi: 10.3390/cancers15030737

Figure 1.

Figure 1

Ripk4 tumor suppressor function is dependent on its kinase activity. (A) Representative image of tumors in Ripk4fl/fl mice transduced with lentivirus (LV) carrying Cre recombinase and green fluorescent protein (GFP). Inlet picture shows the tumor with green fluorescence when imaged under a fluorescent microscope indicating the expression of GFP. (B) Representative mouse image of tumors in Pik3caH1047R;Ripk4fl/fl mice transduced with lentivirus (LV) carrying Cre recombinase. (C) Tumor-free survival for LSL-Pik3caH1047R;Ripk4+/+, LSL-Pik3caH1047R;Ripk4fl/+, LSL-Pik3caH1047R;Ripk4fl/fl mice transduced with LV-Cre (n ≥ 5 per group; p < 0.0001, log-rank test). (D) Western blot analysis of FLAG-tagged Ripk4 proteins (WT: wildtype or K51R: kinase-dead mutant) immuno-precipitated (IP) from primary mouse keratinocytes treated with phosphatase or left untreated. (E) Tumor-free survival for LSL-Pik3caH1047R;Ripk4+/+ and LSL-Pik3caH1047R;Ripk4fl/fl mice transduced either with LV-Cre-tdTomato or LV-Cre-WT Ripk4 or LV-Cre-Ripk4 kinase dead mutant (K51R) (n ≥ 5 per group; p < 0.0001, log-rank test).