Enhancement of the proapoptotic properties of newcastle disease virus promotes tumor remission in syngeneic murine cancer models

Mol Cancer Ther. 2015 May;14(5):1247-58. doi: 10.1158/1535-7163.MCT-14-0913. Epub 2015 Mar 11.


Newcastle disease virus (NDV) is considered a promising agent for cancer therapy due to its oncolytic properties. These include preferential replication in transformed cells, induction of innate and adaptive immune responses within tumors, and cytopathic effects in infected tumor cells due to the activation of apoptosis. To enhance the latter and thus possibly enhance the overall oncolytic activity of NDV, we generated a recombinant NDV encoding the human TNF receptor Fas (rNDV-B1/Fas). rNDV-B1/Fas replicates to similar titers as its wild-type (rNDV-B1) counterpart; however, overexpression of Fas in infected cells leads to higher levels of cytotoxicity correlated with faster and increased apoptosis responses, in which both the intrinsic and extrinsic pathways are activated earlier. Furthermore, in vivo studies in syngeneic murine melanoma models show an enhancement of the oncolytic properties of rNDV-B1/Fas, with major improvements in survival and tumor remission. Altogether, our data suggest that upregulation of the proapoptotic function of NDV is a viable approach to enhance its antitumor properties and adds to the currently known, rationally based strategies to design optimized therapeutic viral vectors for the treatment of cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cell Line, Tumor
  • Chlorocebus aethiops
  • Female
  • HeLa Cells
  • Humans
  • Melanoma, Experimental / immunology
  • Melanoma, Experimental / therapy*
  • Mice
  • NIH 3T3 Cells
  • Newcastle disease virus / genetics
  • Newcastle disease virus / physiology*
  • Oncolytic Virotherapy
  • Oncolytic Viruses / genetics
  • Oncolytic Viruses / physiology
  • Skin Neoplasms / immunology
  • Skin Neoplasms / therapy*
  • Vero Cells
  • fas Receptor / genetics
  • fas Receptor / metabolism*


  • FAS protein, human
  • fas Receptor