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. 2012 Jan 12;106(3):496–507. doi: 10.1038/bjc.2011.577

Table 1. (a) Summary of in vitro therapy data; (b) Interaction of Oncovexgalv/CD and mitomycin C on three TCC cell line; (c) Interaction of Oncovexgalv/CD and cisplatin on three TCC cell line; (d) Interaction of Oncovexgalv/CD and gemcitabine on three TCC cell line.

Cell type Hystological type HSV-1 CPE efficacy Fusion efficacy Prodrug efficacy
(a)
 EJ TCC + + +
 T24 TCC + +
 RT112 TCC + +
 VMCUB-I TCC + +
 TCCSUP-G TCC + +
 5637 TCC + + +
 KU19-19 TCC + +
Cell line ED50 ED70 ED95
(b)
 EJ 0.77±0.05 0.80±0.04 0.86±0.04
 T24 0.65±0.07 0.61±0.04 0.73±0.07
 KU19-19 0.78±0.01 0.58±0.06 0.57±0.08
       
(c)
 EJ 2.6±0.12 2.29±0.01 2.11±0.01
 T24 2.34±0.02 2.03±0.24 1.8±0.4
 TCCSUPG 1.73±0.16 1.28±0.13 1.09±0.21
       
(d)
 EJ 2.92±0.38 2.08±0.24 1.53±0.24
 T24 1.54±0.43 0.89±0.22 0.59±0.12
 TCCSUPG 1.42±0.13 1.18±0.47 1.18±0.78

Abbreviations: CPE=cytopathic effect; HSV=herpes simplex virus; TCC=transitional cell cancer.

The effect of the combination of OncovexGALV/CD and chemotherapy on cell proliferation was assessed by calculating combination index (CI) values using CalcuSyn software (Biosoft). Derived from the median-effect principle of Chou and Talalay, the CI provides a quantitative measure of the degree of interaction between two or more agents. A CI of 1 denotes an additive interaction, >1 antagonism, and <1 synergy. Experiments were done as described for the in vitro survival assay using 4, 2, 1, 0.5, and 0.25 times the calculated ED50 of each agent in a constant ratio checkerboard design.