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. Author manuscript; available in PMC: 2017 Aug 1.
Published in final edited form as: Clin Cancer Res. 2016 Mar 15;22(15):3876–3883. doi: 10.1158/1078-0432.CCR-15-2052

Figure 3. Lack of IL27 signaling stabilizes mutant p53 in vivo and in vitro.

Figure 3

(A) p53 staining via immunohistochemistry of bone marrow vertebral bodies from 8 month old wildtype, IL27RA−/− p53R172H/+ , and IL27RA−/− p53H/+ mice. (B) p53 and p21 staining via immunohistochemistry of bone marrow vertebral bodies from 2, 4, and 8 month old IL27RA−/− p53H/+ mice including a positive control for p21. (C) Bone marrow cells derived from aged wildtype, p53H/+ and IL27RA−/−p53H/+ mice were seeded in a 6-well plate and either irradiated (IR) or left un-irradiated. Cells were collected at the indicated time points and were probed for p53 and actin. (D) H318 and H76 osteosarcoma cells were treated with rIL27 for 30 mins at 20ng/ml and collected lysates were probed for p53 levels and actin,