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. Author manuscript; available in PMC: 2016 May 1.
Published in final edited form as: Mol Cancer Res. 2015 Jan 30;13(5):819–827. doi: 10.1158/1541-7786.MCR-14-0492

Figure 5. Micro-CT assessment to determine the potential of OPGmut in inhibiting tumor-induced osteolytic damage.

Figure 5

Nude mice were injected intratibially with ~1×105 osteolytic prostate cancer cell line PC3. Twenty-four hours later, ~3×105 MSC over-expressing OPGwt, OPGmY49R or OPGmF107A were injected into the same tibia for intratumoral administration and by tail vein injection for systemic administration. Mice from both routes of MSC administration were sacrificed 14 days post MSC therapy and tibia were collected for Micro-CT analysis to determine changes in the overall trabecular architecture (A) and connectivity density (B) (*p<0.05; **p<0.01, compared to Naïve).