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High efficiency, specific targeting, and low-toxic treatments are now in great demand for cancer therapy.In this study, comparative analysis of differential cytopathic effects(CPEs), ultra-structural changes, viral replication and genome transcription were carried out in cancer cell lines, continuous cells(NIH3T3) and primary murine embryo fibroblast (MEF) to test BTV-16s oncolytic ability in vitro.S 180 mice tumor model was used to determine the oncogenicity potential of BTV in vivo.