Abstract
Induction of expression of the tumor suppressor p53 after interferon treatment has been recently demonstrated (Takaoka et al., 2003), suggesting an antiviral activity of the protein. In addition, a direct correlation between p53 levels and tumor resistance has been addressed by generating mice with an extra copy of p53 ('super p53' mice) (Garcia-Cao et al., 2002). Here, we show that vesicular stomatitis virus replication in mouse embryo fibroblasts derived from 'super p53' mice is impaired as a result of apoptosis induction via p53 activation. These findings unequivocally demonstrate an antiviral activity of p53, a process that may contribute to inhibit the spread of the virus in vivo.
| Original language | English |
|---|---|
| Pages (from-to) | 3059-3062 |
| Number of pages | 4 |
| Journal | Oncogene |
| Volume | 24 |
| Issue number | 18 |
| DOIs | |
| State | Published - 21 Apr 2005 |
| Externally published | Yes |
Keywords
- 'Super p53' mice
- Antiviral activity
- Tumor suppressor
- Vaccinia virus
- Vesicular stomatitis virus
- p53
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