Skip to main content
. Author manuscript; available in PMC: 2020 Aug 20.
Published in final edited form as: Mol Cancer Res. 2019 May 14;17(8):1748–1758. doi: 10.1158/1541-7786.MCR-19-0236

Figure 2: Inhibition of TGFβRII signaling reduces primary tumor size and metastasis of CMT-luc cells.

Figure 2:

(A) Western blot for TGFβRII in untransduced parental CMT-luc cells or CMT-luc cells transduced with control or TGFβRII targeting shRNA. (B) qRT-PCR of TGFβRII expression in parental CMT-luc and CMT-luc cells transduced with control shRNA or TGFβRII targeting shRNA (602 or 531). (C,D) WT mice were orthotopically injected with CMT-luc cells expressing control shRNA or the TGFβRII targeting shRNA 602. Mice were harvested to measure metastasis 5 weeks post injection. There were 16 mice injected with the control shRNA CMT-luc cells and 19 mice injected with the TGFβRII targeting shRNA CMT-luc cells. The data for all mice injected is reported. (E,F) WT mice were orthotopically injected with CMT-luc cells and treated with the TGFβRI inhibitor SB431542 (10 mg/kg) or vehicle control (1:1 DMSO:PBS) starting at the time of injection and continuing 5 days a week for 5 weeks. (D,F) Primary tumor size was measured by caliper and reported as the tumor volume in mm3. (E,F) Incidence of metastasis reported as the percent of mice with metastasis to the other lobes of the lung (secondary lung) or liver, as measured by bioluminescence (*p<0.05).