PML isoforms IV and V contribute to adenovirus-mediated oncogenic transformation by functionally inhibiting the tumor-suppressor p53-Reference-Cited by-同舟云学术

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PML isoforms IV and V contribute to adenovirus-mediated oncogenic transformation by functionally inhibiting the tumor-suppressor p53

Published:2015-03-16 Issue:1 Volume:35 Page:69-82
ISSN:0950-9232
Container-title:Oncogene
language:en
Short-container-title:Oncogene

Author:

Wimmer P,Berscheminski J,Blanchette P,Groitl P,Branton P E,Hay R T,Dobner T,Schreiner S

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics,Molecular Biology

Link

http://www.nature.com/articles/onc201563.pdf

Reference139 articles.

1. Carvalho T, Seeler JS, Öhman K, Jordan P, Pettersson U, Akusjärvi G et al. Targeting of adenovirus E1A and E4-ORF3 proteins to nuclear matrix-associated PML bodies. J Cell Biol 1995; 131: 45–56.

2. Maul GG . Nuclear domain 10, the site of DNA virus transcription and replication. Bioessays 1998; 20: 660–667.

3. Ishov AM, Maul GG . The periphery of nuclear domain 10 (ND10) as site of DNA virus deposition. J Cell Biol 1996; 134: 815–826.

4. Ullman AJ, Hearing P . Cellular proteins PML and Daxx mediate an innate antiviral defense antagonized by the adenovirus E4 ORF3 protein. J Virol 2008; 82: 7325–7335.

5. Ullman AJ, Reich NC, Hearing P . Adenovirus E4 ORF3 protein inhibits the interferon-mediated antiviral response. J Virol 2007; 81: 4744–4752.

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