Each of the mice in the 3 treatment groups were injected intratumorally with 100 μL of the respective treatment once every 7 days, for a total of 5 injections. The tumor diameters were measured 2 times per week with a caliper. The tumor volume (mm3) was calculated as: (length × width2)/2. All mice were euthanized humanely after 5 treatments, and the resected tumors were weighed. Statistical analyses Statistical analyses were performed using Statistical Package for the Social Sciences version 16.0 software (SPSS, Chicago, IL). Data were expressed as mean ± standard deviation (SD), and analyzed using the Q-test

or analysis of variance (ANOVA). The level of significance was set at P < 0.05. Results Identification of MOI in glioblastoma cell line U87 To verify the transfection efficiency of Ad-vector in U87 cells, uptake of fluorescently-labeled Ad-vector (MOI 50, 100, 200) was selleckchem detected by fluorescence microscopy 24 and 48 h after transfection. ZD1839 mouse The test showed high-efficiency transfection: > 90% of cells displayed green fluorescence 48 h after transfection with 100 MOI Ad-enhanced GFP (EGFP; Figure 1). Figure 1 Identificcation of MOI in glioblastoma cells. Detection of MOI by fluorescence microscopy. A: under ordinary light; B:

under fluorescence light; C: superimposed image of the two images. Optimal MOI of transfection with Ad-EGFP (green) in U87 cells were easily identified for 48 h post-transfection (×100). Expression of CALR and MAGE-A3 is examined by PCR and see more Western blot To testify to the expression of CALR and MAGE-A3 and examine the differences among the four treatment groups, RT-PCR, qRT-PCR and Western blot were performed. The results of qRT-PCR showed that there were differences in CALR gene expression in U87 cells among the treatment groups. U87 transfected P-type ATPase with Ad-CALR or Ad-CALR/MAGE-A3 expressed higher levels of CALR (Figure 2A). The results of RT-PCR showed that MAGE-A3 was expressed in each treatment group of U87 cells (Figure 2B). However, the transfection

of MAGE-3A in U87 cells, demonstrated by the expression of MAGE-A3/PolyA, was demonstrated only in the Ad-CALR/MAGE-A3-transfected group (Figure 2B). Results of the Western blot indicated that CALR and MAGE-A3 protein was expressed in U87 cells of all treatment groups (Figure 2C). Figure 2 Transfection of Ad-CALR/MAGE-A3 into glioblastoma cells. (A): Comparision of expression of CALR in each group of U87 cells by quantitative RT-PCR. (B): Identification of expression of MAGE-A3 and MAGE-A3/PolyA by RT-PCR. (C): Identification of expression of CALR and MAGE-A3 in each grou of U87 cells by Western blotting. Inhibition of cell proliferation The effect of Ad-CALR/MAGE-A3 transfection on glioblastoma cell proliferation was determined by MTT assay. The inhibition of cell proliferation was calculated as one minus the optical density reading taken at 490 nm.