After a 12 h incubation at 37°C in a 5% CO2 atmosphere, the medium was removed, the cells washed once with PBS, added with fresh complete D-MEM and incubated at 32°C with 5% CO2 for 48 h. The medium containing the E5 bearing – or the empty, negative control, -retroviral progenies were removed and centrifuged at 1000 × g for 10 min to pellet cell debris. Clarified supernatant were harvested and either used immediately for infection or aliquoted and stored at -80°C for later use. Infection procedure 24 h before infection, melanoma cells were harvested and replated at 2.0 × 104 cell/cm2 into T-25 flasks. The infection mixtures were prepared

by adding 1.5 ml of D-MEM containing either the E5 retrovirus or the empty selleck screening library retrovirus with 1.5 ml of complete D-MEM. Polybrene (5 μg/ml) was then added to each flask directly at the moment of infection. Flasks were then centrifuged at 190 × g for 30 min

at room temperature and incubated for 24 h at 32°C in a 5% CO2 atmosphere. The medium was then changed with fresh, complete D-MEM and the cells incubated at 37°C with 5% CO2 for further 48 h. Surviving cells, roughly 40% of the challenged cells, were then washed twice with PBS and replated at 2 × 104 cell/cm2. The efficiency of infection procedure was measured in a pilot experiment by a dilution limit PCR strategy showing an almost even end point for E5 and the single copy beta-globin reference PS341 sequence (data not shown). This finding is compatible with an above 50% infection of target cells FG-4592 mw carrying 1 to 10 copies of proviral DNAs and is in tune with the results expected on the basis of theoretical considerations. The presence of the proviral E5 Aldol condensation DNA and of the E5 specific mRNA was confirmed by PCR and RT-PCR as below described. Cells infected with the control retrovirus were briefly referred to as “”control cells”" throughout the paper. PCR and RT-PCR Analyses were performed as previously described [27]. Total DNA and RNA were simultaneously

extracted from exponentially growing cell cultures by the Tri-Reagent commercial kit (Molecular Research Centre, Cincinnati, OH) used according to the supplier’s instruction. The quality of RNAs was evaluated by the A260/A280 ratio and by visual inspection of ethidium bromide stained formamide agarose gel electrophoresis under UV-B trans-illumination. 1 μg of DNAse digested total RNA and 0.2 μg DNA were amplified in a 50 μl volume of Superscript One-Step (RT)-PCR Platinum TAQ reaction mixture completed with 500 nM up-stream and down-stream primers and 1.5 mM Mg2+. For RT-PCR, the reverse transcription was carried out at 45°C for 30 min. Samples were then heated to 95°C for 150 s to inactivate reverse transcriptase and to activate Platinum TAQ Polymerase. Amplification consisted in 35 cycles under the following conditions. For E5: annealing at 94°C for 50 s, extension at 45°C for 50 s and denaturation at 72°C for 60 s and a final cycle with a 10 min long extension.