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. 2018 Apr 26;16:110. doi: 10.1186/s12967-018-1483-x

Fig. 5.

Fig. 5

Virus-encoded luciferase activity correlates with tumor regression over time and increasing viral titers in the non-injected tumors. To ensure luciferase visualization, CF33-Fluc was administered at 104 PFU to PANC-1 xenograft-bearing immune-compromised mice. a Relative luciferase activity decreased in the injected tumors and increased in the non-injected distant tumor over time. b Percent change in CF33-Fluc-injected tumor size and luciferase activity were correlated (R2 = 0.879). c CF33-Fluc enabled real time in vivo monitoring of viral replication at days 3, 13 and 27 and showed replication in both the injected and non-injected distant tumors. d CF33-Fluc titers in the injected tumors are at least 4 logs higher than in other organs, indicating early preferential replication in tumors. Virus titers in the non-injected tumors increased over time, which correlates to luciferase activity