| Literature DB >> 22805590 |
David Pim1, Martina Bergant1, Siaw S Boon1, Ketaki Ganti1, Christian Kranjec1, Paola Massimi1, Vanitha K Subbaiah1, Miranda Thomas1, Vjekoslav Tomaić1, Lawrence Banks1.
Abstract
The human papillomavirus (HPV) E6 oncoprotein is fundamental to the ability of these viruses to induce human malignancy. A defining characteristic of the HPV E6 oncoproteins found in cancer-causing HPV types is the presence of a PDZ binding motif at their extreme C-terminus. Through this motif, E6 is able to interact with a large number of cellular proteins that contain PDZ domains. Many of these cellular proteins are involved in regulation of processes associated with the control of cell attachment, cell proliferation, cell polarity and cell signaling. How E6 targets multiple proteins containing the same recognition domain is still an open question. In this review, we highlight aspects of E6 function and biology that help to answer this question, and thereby provide insight into the role of these substrates during development of HPV-induced malignancy.Entities:
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Year: 2012 PMID: 22805590 DOI: 10.1111/j.1742-4658.2012.08709.x
Source DB: PubMed Journal: FEBS J ISSN: 1742-464X Impact factor: 5.542