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Science 6 April 1990:
Vol. 248. no. 4951, pp. 76 - 79
DOI: 10.1126/science.2157286

Articles

Science, Vol 248, Issue 4951, 76-79
Copyright © 1990 by American Association for the Advancement of Science


articles

Association of human papillomavirus types 16 and 18 E6 proteins with p53

BA Werness, AJ Levine, and PM Howley

Laboratory of Tumor Virus Biology, National Cancer Institute, Bethesda, MD 20892.

Human papillomavirus type 16 (HPV-16) is a DNA tumor virus that is associated with human anogenital cancers and encodes two transforming proteins, E6 and E7. The E7 protein has been shown to bind to the retinoblastoma tumor suppressor gene product, pRB. This study shows that the E6 protein of HPV-16 is capable of binding to the cellular p53 protein. The ability of the E6 proteins from different human papillomaviruses to form complexes with p53 was assayed and found to correlate with the in vivo clinical behavior and the in vitro transforming activity of these different papillomaviruses. The wild-type p53 protein has tumor suppressor properties and has also been found in association with large T antigen and the E1B 55-kilodalton protein in cells transformed by SV40 and by adenovirus type 5, respectively, providing further evidence that the human papillomaviruses, the adenoviruses, and SV40 may effect similar cellular pathways in transformation.


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Depletion of Langerhans Cells in Human Papillomavirus Type 16-Infected Skin Is Associated with E6-Mediated Down Regulation of E-Cadherin.
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J. Virol. 76, 13039-13048
   Abstract »    Full Text »    PDF »
The Human Papillomavirus Type 16 E5 Protein Impairs TRAIL- and FasL-Mediated Apoptosis in HaCaT Cells by Different Mechanisms.
K. Kabsch and A. Alonso (2002)
J. Virol. 76, 12162-12172
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Establishment of an HLA-A*0201 Human Papillomavirus Type 16 Tumor Model to Determine the Efficacy of Vaccination Strategies in HLA-A*0201 Transgenic Mice.
G. L. Eiben, M. P. Velders, H. Schreiber, M. C. Cassetti, J. K. Pullen, L. R. Smith, and W. M. Kast (2002)
Cancer Res. 62, 5792-5799
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Modulation of the Cell Division Cycle by Human Papillomavirus Type 18 E4.
T. Nakahara, A. Nishimura, M. Tanaka, T. Ueno, A. Ishimoto, and H. Sakai (2002)
J. Virol. 76, 10914-10920
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The Upstream Regulatory Region of Human Papillomavirus Type 31 Is Insensitive to Glucocorticoid Induction.
J. L. Bromberg-White and C. Meyers (2002)
J. Virol. 76, 9702-9715
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Transcriptional Regulation of the mdm2 Oncogene by p53 Requires TRRAP Acetyltransferase Complexes.
P. G. Ard, C. Chatterjee, S. Kunjibettu, L. R. Adside, L. E. Gralinski, and S. B. McMahon (2002)
Mol. Cell. Biol. 22, 5650-5661
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Human Papillomavirus Oncoprotein E6 Inactivates the Transcriptional Coactivator Human ADA3.
A. Kumar, Y. Zhao, G. Meng, M. Zeng, S. Srinivasan, L. M