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. 2015 Apr 22;3:55. doi: 10.3389/fbioe.2015.00055

Table 1.

In vitro evidence of H-1PV oncoselectivity.

Transformed/tumor cells (Tu) Normal cells (N) Tu versus N sensitization to H-1PV infection Reference
Spontaneously transformed human amnion Normal human amniona
  • CPE in Tu

  • No toxicity in N

Toolan and Ledinko (1965)
SV40-transformed human (fore)skin fibroblasts Normal human (fore)skin fibroblastsa
  • Efficient Tu killing: active DNA and protein synthesis; abundant NS1 phosphorylation; productive Tu infection

  • Minor cytotoxicity, no killing and abortive N infection

Chen et al. (1986, 1989), Faisst et al. (1989), Dupressoir et al. (1989), Van Pachterbeke et al. (1993, 1997), and Muharram et al. (2010)
Squamous cell carcinoma-derived human keratinocytes Normal human breast skin keratinocytesa
Breast carcinoma-derived human epithelial cells Normal human mammary gland epithelial cellsa
Hepatoma-derived human cells Normal human hepatocytesa
  • Tu killing through apoptosis

  • No NS1 expression and no N killing

Moehler et al. (2001)
Glioma-derived human cells Normal human astrocytes and gliaa
  • Cathepsin-mediated Tu death

  • Low NS1 levels and no N killing

Di Piazza et al. (2007) and Lacroix et al. (2010, 2014)
EBV-transformed and lymphoma/leukemia-derived human immune cells Normal human and rat immune cellsa
  • Efficient Tu killing and productive Tu infection

  • Retained N viability and abortive N infection

Moehler et al. (2003), Angelova et al. (2009a), Grekova et al. (2010a,b), Moralès et al. (2012), and Raykov et al. (2013)

aNon-established (low-passage-number) cultures.

CPE, cytopathic effect; EBV, Epstein–Barr virus.