
Recent reports suggest promises on using oncolytic Newcastle disease viruses (NDV) to treat different cancers, while the effects of a NDV-D90 strain on gastric cancer remain unknown. Here we showed that NDV-D90 induced gastric cancer cell apoptosis in a dose-dependent manner in 3 gastric cancer cell lines BGC-823, SGC-7901 and MKN-28. Pronounced reduction in cell invasion was detected in NDV-D90-treated BGC-823 and SGC-7901 cells, but not in MKN-28 cells. The increases in cell apoptosis and reduction in cell growth in NDV-D90-treated gastric cancer cells seemingly resulted from augmentation of p38 signaling and suppression of ERK1/2 and Akt signaling. In vivo, orthotopic injection of NDV-D90 impaired tumor growth and induced intratumoral necrosis. Tumor cells that had been pre-treated with NDV-D90 showed defect in development of implanted tumor. Moreover, NDV-D90 appeared to reduce gastric tumor vascularization, possibly through suppression of vascular endothelial growth factor A and Matrix Metallopeptidase 2. Together, our data suggest that NDV-D90 may have potential anti-cancer effects on gastric cancer.
Oncolytic Virotherapy, Neovascularization, Pathologic, Cell Survival, MAP Kinase Signaling System, Newcastle disease virus, Xenograft Model Antitumor Assays, Mice, Stomach Neoplasms, Cell Line, Tumor, Animals, Humans, Neoplasm Invasiveness, Research Paper, Cell Proliferation
Oncolytic Virotherapy, Neovascularization, Pathologic, Cell Survival, MAP Kinase Signaling System, Newcastle disease virus, Xenograft Model Antitumor Assays, Mice, Stomach Neoplasms, Cell Line, Tumor, Animals, Humans, Neoplasm Invasiveness, Research Paper, Cell Proliferation
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
