Newcastle Disease Virus Mediated Apoptosis And Migration Inhibition Of Human Oral Cancer Cells: A Probable Role Of Beta-Catenin And Matrix Metalloproteinase-7

Cancer cell metastasis and its dissemination are most enigmatic and challenging aspects in the development of its therapeutics. Newcastle disease virus (NDV) is a well-studied avian paramyxovirus frequently isolated from birds and rarely from mammals. Since the first report of its oncolytic property, many NDV strains were studied for its effect in various cancer cells. In the present study, NDV strain Bareilly was characterized for its apoptotic potential and migration inhibition in human oral cancer cells. The NDV mediated apoptosis was confirmed by flow cytometry, DNA laddering, and immunoblotting. Moreover, NDV decreased the mitochondrial membrane potential suggesting an intrinsic pathway of apoptosis in oral cancer cells. NDV infection in oral cancer cells results in migration inhibition by a reduction in levels of MMP-7. MMP-7 is one of the key target genes of beta-catenin. While overexpression of MMP-7 reversed the inhibitory effect of NDV mediated migration suggested its possible involvement. Wnt/beta-catenin is an essential pathway for cell growth, differentiation, and metastasis. The involvement of the Wnt/beta-catenin pathway in NDV infection has never been reported. Our results showed that NDV dysregulates Wnt/beta-catenin by down-regulation of p-Akt and p-GSK3 beta leading to degradation of beta-catenin. Furthermore, NDV infection leads to a reduction in cytoplasmic and nuclear levels of beta-catenin. The study will provide us with a better insight into the molecular mechanism of NDV mediated oncolysis and the key cellular partners involved in the process.