Ontology highlight
ABSTRACT: Background
M protein mutant vesicular stomatitis virus (M51R-VSV) has oncolytic properties against many cancers. However, some cancer cells are resistant to M51R-VSV. Herein, we evaluate the molecular determinants of vesicular stomatitis virus (VSV) resistance in pancreatic adenocarcinoma cells.Methods
Cell viability and the effect of β-interferon (IFN) were analyzed using 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium assay. Gene expression was evaluated via microarray analysis. Cell infectability was measured by flow cytometry. Xenografts were established in athymic nude mice and treated with intratumoral M51R-VSV.Results
Four of five pancreatic cancer cell lines were sensitive to M51R-VSV, whereas Panc 03.27 cells remaine
SUBMITTER: Blackham AU
PROVIDER: S-EPMC3959227 | biostudies-literature | 2014 Apr
REPOSITORIES: biostudies-literature