Detection of adenoviruses in cells SW480 and LoVo cells as well as intestinal epithelial cells (IEC) were plated at 105 cells per 6 cm dish and infected with ZD55-Sur-EGFP or AD-Sur-EGFP for 48 h and 72 h. The expression of enhanced green fluorescent protein (EGFP) was accessed by a Zeiss fluorescence microscope coupled with a digital camera photo apparatus. RT-PCR analysis Total RNA from transfected cells was isolated using TRIzol (Invitrogen) as recommended

by the manufacturer. RT-PCR was used for the analysis of Survivin mRNA with GAPDH as an internal Panobinostat control. Primers for Survivin were as follow: forward primer 5′-GAC CAC CGC ATC TCT ACA TTC-3′, reverse primer 5′-GTT CTT GGC TCT TTC TCT GTCC-3′. The GAPDH primers were forward 5′-ACC ACA GTC CAT GCC ATC AC-3′ and reverse 5′-TCC ACC ACC CTG TTG CTG TA-3′. Reactions were performed in accordance with the standard protocol. PCR was performed Selleckchem Kinase Inhibitor Library by initial denaturation at 94°C for

5 min followed by 35 cycles of 30 s at 94°C, 30 s at 58°C and 60 s at 72°C. The products were separated by electrophoresis in 2% agarose and visualized with ethidium bromide. Experiments were performed in triplicate. Western blot analysis Cells were transfected with adenoviruses and incubated for 48 h. After that they were harvested and the protein extracts were separated via sodium dodecyl sulfate-polyacdene gel electrophoresis and transferred onto nitrocellulose membranes. The membranes were then blocked with rabbit anti-Survivin, Ad2 E1A, β-actin (Santa Cruz), XIAP (Sigma) and caspase-3 (Beyotime, China) primary polyclonal antibodies respectively at 4°C overnight. After washing with PBS 3-oxoacyl-(acyl-carrier-protein) reductase containing 0.05% Tween 20 the membranes

were incubated with secondary antibody (goat anti-rabbit, Santa Cruz) for 2 h. They were visualized by chemiluminescence system according to manufacturer’s instruction. In vitro cytopathic assay Cells were grown subconfluently and infected with adenoviruses with indicated MOIs. 5 days later, the medium was removed and the cells were washed with PBS twice, exposed to Coomassie brilliant blue and then washed with distilled water. The result was documented as photographs. MTT cell viability assay To quantify the cytopathic effect, MTT assay was performed. Cells were seeded in 96-well plates for 24 h at 1 × 104 per well. After 1 to 5 days of various viruses infection, 15 μl MTT (5 mg/ml in PBS) was added to each well for 4 h incubation at 37°C followed by the addition of 150 μl DMSO. Absorbance at 570 nm was measured for cell viability in each well. Flow cytometry evaluation Apoptosis of cells infected with adenoviruses at MOI of 5 was determined by flow cytometry (FCM) using Annexin V: PE Apoptosis Detection Kit I (BD Biosciences, USA) according to manufacturer’s instruction. Briefly, Cells were washed twice with cold PBS and resuspended in binding buffer at a concentration of 1 × 105 cells/ml.