Yuan B , Xian R , Ma J , Chen Y , Lin C , Song Y .

             negative regulation of angiogenesis

	Fig. 1. a The expression of isthmin in U251 cells was analyzed by western blot analysis. U251 cells were transduced with Ad-isthmin or Ad-LacZ at an MOI of 200 for 24 h. The expression of isthmin increased significantly after Ad-isthmin transfection. However, the expression of isthmin after Ad-LacZ transduction and non-treated U251 cells could not be detected. b The expression of isthmin was analyzed by semi-quantitative western blot using β-actin for standardization. 1 non-treated U251 cells, 2 U251 cells transduced with Ad-LacZ, 3 U251 cells transduced with Ad-isthmin
	Fig. 2. Inhibitory effect of Ad-Isthmin on cell proliferation. a HUVECs or U251 cells were seeded in 96-well plates at 5 × 103 cells/well and incubated in culture medium overnight. The cells were transduced with Ad-isthmin (1 × 109 pfu) or controls for 24 h. b U251 cells were seeded in 96-well plates at 5 × 103 cells/well and incubated in culture medium overnight. The cells were transduced with Ad-isthmin (1 × 109 pfu) or controls for 24 h. The supernatant were harvested and cocultured with HUVECs with the similar method. Then MTT solution (5 mg/mL) was added and cultured for 48 h. The colored formazan crystal produced from MTT was dissolved with 0.15 mL DMSO then the optical density (OD) value A490 was measured. The data are the averages from three independent triplicate experiments. *P < 0.05 compared with control groups
	Fig. 3. Ad-isthmin induces cell apoptosis in vitro. 2 days after transduction of Ad-isthmin, Ad-LacZ or PBS, Annexin V-fluoresceinisothiocyanate (0.5 mg/mL) and propidium iodide (0.5 mg/mL) were then added to a 250-mL aliquot (5 × 106 cells) of this cell suspension. After 15 min incubation in the dark at room temperature, stained cells were immediately analyzed by Flow Cytometry (Coulter Biosciences). Apoptosis cells were determined by AnnexinV-positive and propidium iodide (PI)-negative cells. The data are the averages from three independent triplicate experiments. *P < 0.05 compared with control groups
	Fig. 4. Analysis of caspase-3 activities. The variation of caspase-3 activities in HUVECs was measured using caspase colorimetric assay kit. After the HUVECs were transduced with Ad-isthmin, Ad-LacZ, or PBS, the cell lysates were tested for protease activity using a caspase-specific peptide, conjugated to the color reporter molecule p-nitroanaline. The chromophore p-nitroanaline, cleaved by caspases, was quantitated with a spectrophotometer at a wavelength of 405 nm. The caspase enzymatic activities in cell lysate were directly proportional to the color reaction. The data are the averages from three independent triplicate experiments. *P < 0.05 compared with control groups
	Fig. 5. Ad-isthmin inhibits tumor growth of nude mice. a Eight-week-old nude mice were challenged with subcutaneous (s.c) injection of 1 × 105 U251 glioma cells into the right flank to induce primary tumors. Seven days after tumor cell inoculation, mice were divided randomly and were received an intratumor injection of Ad-isthmin (1 × 109 pfu), Ad-LacZ (1 × 109 pfu), or 100 μL PBS (10 mice per group). Tumor volume was measured in two dimensions and calculated as follows: length/2 × width2. b Eight-week-old nude mice were challenged with intracerebral injection of 1 × 106 U251 glioma cells into the basal ganglia of the mice. One day after tumor cell inoculation, mice were divided randomly and were received an intracerebral delivery of Ad-isthmin (1 × 109 pfu), Ad-LacZ (1 × 109 pfu), or 5 μL PBS (10 mice per group). Fifteen days after the tumor challenge, the mice were killed. Mouse brains were removed, fixed and embedded. Serial sections (5 μm thick) were stained with hematoxylin-eosin (HE). Tumor volume was estimated as follows: (square root of maximal tumor cross-sectional area)3. c Representative HE staining section of mouse brain after intracerebral injection of U251 glioma cells. d Percent survival of nude mice challenged with intracerebral injection of 1 × 106 U251 glioma cells (10 mice per group). The data are the averages from three independent triplicate experiments
	Fig. 6. Inhibition of angiogenesis in the tumor tissue. 21 days after the tumor challenge, the mice were sacrificed, and the tumor tissues were fixed in acetone, and stained with an antibody reactive to CD31 as described for microvessel density (MVD) analysis. a Vessel density was determined by counting the number of the microvessels per high-power field in tumor sections stained with antibody reactive to CD31. b The representative immuno histochemical analysis of CD31 expression in the tumor of Ad-isthmin and control groups. The data are the averages from three independent triplicate experiments. *P < 0.05 compared with control groups

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