The potential use of oncolytic viruses in the treatment of cancer has been
investigated for some time. A variety of agents have been studied, includin
g some which appear to be selectively replication-competent in cancer cell
lines. In this study, we have investigated the ability of herpesvirus saimi
ri to specifically lyse selected human cancer cell lines. Upon infection wi
th a replication-competent virus carrying the EGFP reporter gene and a neom
ycin resistance marker, the pancreatic cancer lines MIAPACA and PANC-1 exhi
bited definite cytopathic effects, in contrast, the colonic carcinoma cell
lines SW480 and HCT116 were phenotypically unaltered. in addition, stable c
ell lines could not be generated from PANG-I infected cultures, in marked c
ontrast to cultures of cells from other human tissues. Virus recovery assay
s demonstrated that all of the cell lines produced a small amount of virus
post-infection, but that virus replication was minimal after 1 week in cult
ure. in addition, treatment with acyclovir inhibited Virus replication but
paradoxically increased cytopathic effect. These data suggest that herpesvi
rus saimiri may have potential as an oncolytic agent for the treatment of p
ancreatic cancer. (C) 2000 Cancer Research Campaign.