Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2114689 | Cancer Letters | 2009 | 7 Pages |
Abstract
The p53 plays critical role in cellular functions such as cell cycle arrest and apoptosis. We overexpressed wild-type p53 (wt-p53) in U87 glioblastoma cells via recombinant adenovirus Ad-GFP-P53 which encodes p53 and green fluorescent protein. The transcript profiles were investigated using cDNA amplified fragment length polymorphism approach. Semi-quantitative RT-PCR and DNA sequencing results for the selected genes showed that Cathepsin B and cell cycle associated protein-1 or Caprin-I, genes were suppressed whereas Annexin-II gene overexpressed in response to the overexpression of wt-p53 gene. Our results suggest that these genes could be important mediators of p53-dependent tumor growth suppression in glioblastoma.
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Authors
Mojtaba Saffari, Orkideh Saydi Dinehkabodi, Seyed Hamid Ghaffari, Mohammad H. Modarressi, Fatemeh Mansouri, Mansour Heidari,