Newcastle disease virus lasota strain kills human pancreatic cancer cells in vitro with high selectivity

Robert J. Walter, Bashar M. Attar, Asad Rafiq, Sooraj Lakshmi Tejaswi, Megan Delimata

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


Context Pancreatic cancer is highly resistant to treatment. Previously, we showed that Newcastle disease virus (NDV) strain 73-T was highly cytotoxic to a range of tumor types in vitro and in vivo but the effects of NDV on pancreatic tumors are unknown. We determined the cytotoxicity of the lentogenic LaSota strain of NDV (NDV-LS) toward 7 different human pancreatic tumor cell lines and 4 normal human cell lines (keratinocytes, fibroblasts, pancreatic ductal cells, and vascular endothelial cells). Methods Cytotoxicity assays used serially diluted NDV incubated for 96 hours post-infection. Cells were fixed, stained, and minimum cytotoxic plaque forming unit (PFU) doses were determined (n=10-24/cell line). Results Normal cells were killed only by high doses of NDV-LS. The cytotoxic doses for pancreatic ductal cells, fibroblasts, and vascular endothelial cells were 729, 626, and 1,217 plaque forming units, respectively. In contrast, most pancreatic cancer cells were killed by much lower doses. The doses for PL45, Panc 10.05, PANC-1, BxPC3, SU.86.86, Capan-1 and CFPAC-1 were 0.15, 0.41, 0.43, 0.55, 1.30, 17.1 and 153 plaque forming units, respectively. Conclusions Most pancreatic tumor cells were more than 700 times more sensitive to NDV-LS killing than normal cells. Such avirulent, lentogenic NDV strains may have therapeutic potential in the treatment of pancreatic cancers.

Original languageEnglish (US)
Pages (from-to)45-53
Number of pages9
JournalJournal of the Pancreas
Issue number1
StatePublished - Jan 2012
Externally publishedYes


  • La sota vaccine
  • Neoplasms
  • Newcastle disease virus
  • Newcastle disease virus vaccine MTH-68-H
  • Oncolytic virotherapy
  • Oncolytic viruses
  • Pancreatic neoplasms
  • Paramyxovirus
  • Serine proteases
  • Trypsin
  • V protein
  • Vaccines
  • Viral fusion proteins

ASJC Scopus subject areas

  • Endocrinology
  • Endocrinology, Diabetes and Metabolism
  • Hepatology


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