el approach to develop more effective virotherapies for the treatment of human tumors. Methods Viruses and Cell lines The Ad serotypes Ad3, 
Ad4, Ad5, Ad9, Ad16 and the tumor cell lines A549, PC-3, HT-29, DLD-1, LS1034, HCT116, LS174T, SW48, SW403, Colo320DM, OVCAR-3, DU-145 were all purchased from the ATCC. HEK293s were licensed from McMaster Univeristy. MDA-231mt1 and Panc-sct were derived from rapidly growing subcutaneously implanted xenograft by Drs. Deb Zajchowski and Sandra Biroc at Berlex Biosciences, respectively. Human umbilical vein endothelial cells, and human mammary epithelial cells were grown as per vendors instructions and Ad11p, and Ad40 were kind gifts from Dr. William S.M. Wold at St. Louis University. The replication defective ColoAd1 was derived by homologous recombination of ColoAd1 into a pBRderived plasmid in BJ5183 bacteria using methods as previously described. Viral Purification and Quantitation Viral stocks were propagated on HEK293 cells, with the exception of the replication-defective ColoAd1 which was propagated on A549 cells expressing the E1A and E1B regions of ColoAd1, and purified on CsCl gradients. The method used to quantitate and partially characterize viral particles is based on that of Shabram et al, with the exception that the anion-exchange media TMAE Fractogel was used instead of Resource Q. Cytolytic assay The viral lytic capacity was measured using a modification of the MTT assay. Briefly, the MTS assay was used in place of the MTT 19770292 assay because conversion of MTS by cells into aqueous, soluble formazan reduces time and eliminates the use of a volatile organic solvent associated with the MTT assay. To perform the assay, cells were seeded at a density determined for each tumor cell line to generate a confluent monolayer within 24 hr. These densely seeded cells were allowed to grow for two additional days prior to exposure to the test virus. Infections of both tumor and primary normal cells were carried out in quadruplicate, using serial three fold dilutions of the viruses starting at a particle per cell ratio of 100 and ending at a particle per cell ratio of 0.005 with the exception of MTS assays on HUVEC or HMEC cells which were done starting at a particle per cell ratio of 10,000 for purposes of calculating an in vitro therapeutic index. ARN-509 site infected cells were incubated at 37uC and the MTS assay was performed at the time points indicated for the individual primary cells or tumor cell lines. Mock-infected cells served as negative controls and established the 100% survival point for the given assay. lines at a particle-per-cell ratio of approximately 200 to invite recombination between serotypes. Supernatants from the second round of the high viral particle-per-cell infection of subconfluent cultures were then used in a 10-fold dilution series to infect confluent T-75 tissue culture flasks of target tumor cell lines PC-3, HT-29, Panc-1 and MDA-231. To achieve confluency, each cell line was seeded at split ratios that allowed that cell line to reach confluency between 24 and 40 hours post seeding, and the cells were allowed to grow a total of 72 hours 18347139 post seeding prior to infection. This was done to maximize the confluency of the cells attempting to mimic growth conditions in human solid tumors. The infected T75s were observed for the first signs of cytopathic effect. In order to harvest the most potent viruses, cell culture supernatant was harvested from the flask infected with the most concentrate