Antineoplastic activity of Newcastle disease virus strain D90 in oral squamous cell carcinoma

Tumour Biol. 2015 Sep;36(9):7121-31. doi: 10.1007/s13277-015-3433-z. Epub 2015 Apr 16.

Abstract

Newcastle disease virus (NDV), an avian paramyxovirus, possesses the ability to kill tumor cells. Here, we report the effects of NDV strain D90, which was isolated in China, against oral squamous cell carcinoma (OSCC) cells. In this study, we showed that the cell death induced by D90 was apoptotic. Furthermore, the apoptosis induced by D90 was dependent on the mitochondrial pathway, and the death receptor pathway may be not involved. Bax and Bcl-2 also played a role in the apoptosis induced by D90. Lymph node metastasis is a serious problem for oral cancer; we therefore evaluated the impact of D90 on the migration and invasion of OSCC cells. NDV D90 affected microtubules and microfilaments to inhibit the motility of OSCC prior to apoptosis. The effects of D90 on the migration and invasion rates of OSCC cells were evaluated by migration and invasion assays. Subsequently, the changes in sp1, RECK, MMP-2, and MMP-9 induced by a low concentration of D90 were detected by western blot and gelatin zymography. D90 significantly inhibited the invasion and metastasis of OSCC cells by decreasing the expression of sp1 and increasing the expression of RECK to suppress the expression and activity of MMP-2 and MMP-9.

Keywords: Apoptosis; Invasion; Migration; Newcastle disease virus (NDV); Oral squamous cell carcinoma (OSCC).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Carcinoma, Squamous Cell / genetics
  • Carcinoma, Squamous Cell / pathology
  • Carcinoma, Squamous Cell / therapy*
  • Cell Line, Tumor
  • Cell Movement / genetics
  • GPI-Linked Proteins / biosynthesis*
  • GPI-Linked Proteins / genetics
  • Humans
  • Lymphatic Metastasis
  • Matrix Metalloproteinase 2 / biosynthesis*
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 9 / biosynthesis*
  • Matrix Metalloproteinase 9 / genetics
  • Mitochondria / genetics
  • Mitochondria / metabolism
  • Mouth Neoplasms / genetics
  • Mouth Neoplasms / pathology
  • Mouth Neoplasms / therapy*
  • Neoplasm Invasiveness / genetics
  • Neoplasm Invasiveness / pathology
  • Newcastle disease virus / genetics*
  • Oncolytic Virotherapy
  • Sp1 Transcription Factor / biosynthesis

Substances

  • GPI-Linked Proteins
  • RECK protein, human
  • Sp1 Transcription Factor
  • SP1 protein, human
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9