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The adenovirus E4orf4 protein selectively kills human cancer cells independently of p53 and thus represents a potentially promising tool for the development of novel antitumor therapies. Previous studies suggested that E4orf4 induces an arrest or a delay in mitosis and that both this effect and subsequent cell death rely largely on an interaction with the B55 regulatory subunit of protein phosphatase 2A. In the present report, we show that the death of human H1299 lung carcinoma cells induced by expression of E4orf4 is typified not by an accumulation of cells arrested in mitosis but rather by the presence of both tetraploid and diploid cells that are arrested in G1 because they are unable to initiate DNA synthesis. We believe that these E4orf4-expressing cells eventually die by various processes, including those resulting from mitotic catastrophe.

journal of virology

Adenovirus E4orf4 Protein-Induced Death of p53 <sup>−/−</sup> H1299 Human Cancer Cells Follows a G <sub>1</sub> Arrest of both Tetraploid and Diploid Cells due to a Failure To Initiate DNA Synthesis

Adenovirus E4orf4 Protein-Induced Death of p53 −/− H1299 Human Cancer Cells Follows a G 1 Arrest of both Tetraploid and Diploid Cells due to a Failure To Initiate DNA Synthesis

Adenovirus E4orf4 Protein-Induced Death of p53 ^−/− H1299 Human Cancer Cells Follows a G ₁ Arrest of both Tetraploid and Diploid Cells due to a Failure To Initiate DNA Synthesis