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PMID: 8393818 Published · ppublish English Journal Article Review

Interactions of human papillomavirus transforming proteins with the products of tumor suppressor genes.

Vousden K

Abstract

Human papillomaviruses (HPVs) contribute to the development of almost all cervical cancers, a common and often fatal human disease. The mechanisms by which the HPVs function in malignant progression appear to be related to the activity of the two viral oncoproteins, E6 and E7, which form complexes with several cell proteins normally involved in controlling cell growth. Of particular interest has been the association of E6 with p53 and E7 with Rb, both products of tumor suppressor genes. Expression of E6 and E7 is likely to overcome the regulation of cell proliferation normally mediated by proteins like p53 and Rb, allowing uncontrolled growth and providing the potential for malignant transformation. These activities of E6 and E7 support the importance of the tumor suppressor proteins in the maintenance of normal cell proliferation and provide novel approaches to understanding the mechanisms by which they function.

MeSH Terms
Animals Cell Transformation, Viral DNA-Binding Proteins Humans Oncogene Proteins, Viral/metabolism Papillomaviridae/genetics,metabolism Papillomavirus E7 Proteins Repressor Proteins Retinoblastoma Protein/genetics,metabolism Tumor Suppressor Protein p53/genetics,metabolism
Chemicals
DNA-Binding Proteins E6 protein, Human papillomavirus type 16 E6 protein, Human papillomavirus type 18 E7 protein, Human papillomavirus type 18 Oncogene Proteins, Viral Papillomavirus E7 Proteins Repressor Proteins Retinoblastoma Protein Tumor Suppressor Protein p53 oncogene protein E7, Human papillomavirus type 16
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Vousden K
Ludwig Institute for Cancer Research, St. Mary's Hospital Medical School, London.
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
0892-6638
Published
1993-07-00
Pages
872-9
Language
English
Region
United States
NLM ID
8804484
Subset
IM
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