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. Author manuscript; available in PMC: 2019 Oct 18.
Published in final edited form as: Clin Cancer Res. 2018 Mar 6;24(11):2574–2584. doi: 10.1158/1078-0432.CCR-17-2954

Table 1.

50% Effective dose of oHSV in GBM and non-GBM cell lines

MOI (×10−3), 95% Confidence intervals
rHSVQ
NG34
ED50 R-Seq ED50 R-Seq
U251 22.67 – 47.63 0.8947 2.620 – 5.436 0.8728
U2OS 15.11 – 41.57 0.7516 7.172 – 15.90 0.8516
G9Rluc 34.63 – 70.44 0.9173 4.827 – 7.922 0.9587
G30 9.439 – 16.87 0.9392 1.962 – 3.150 0.9588
G83 25.08 – 54.51 0.9028 4.424 – 9.737 0.8810
G326 17.87 – 43.33 0.8850 3.564 – 7.058 0.9237
G528 86.39 – 270.7 0.6973 26.66 – 64.31 0.8706

NOTE: Enhanced glioma cytotoxicity effect with GADD34-encoding γ134.5-null NG34 versus original γ134.5-null rHSVQ virus. Intracellular ATP was measured 3 days after oHSV infection with either rHSVQ or NG34 or rQNestin34.5 in GBM (U251, G9Rluc and G30) and non-GBM (U2OS) cells at 20,000 cells per a well of 96-well plates for cell viability assay. Data with three replicates were normalized with maximum and minimum values before calculating ranges of 50% effective doses (ED50) and values of R2 at 95% confidence intervals. These plots with nonlinear dose–response curves are also provided in Supplementary Fig. S1.