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PMID: 17854024 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Activities of human papillomavirus 16 E6 natural variants in human keratinocytes.

Journal of medical virology ·Vol. 79 ·No. 11 ·2007-11-00 ·Pages 1751-60

Asadurian Y, Kurilin H, Lichtig H, Jackman A, Gonen P, Tommasino M, Zehbe I, Sherman L

Abstract

Genetic variations in the E6 oncogene have been associated with different risk for cancer progression. In the present study, the functional significance of human papillomavirus (HPV) polymorphism in the E6 oncogene was investigated. Ten HPV16 E6 variants containing amino acid substitutions in the N-terminal region of E6 were evaluated for different biological and biochemical activities in human keratinocytes, the target cells for HPV infection. Western blot analyses of primary foreskin human keratinocytes or immortalized human keratinocytes, stably transduced with the E6 variants, revealed reduced p53 and Bax levels in all E6 expressing cultures. The reduction induced by most E6 proteins was at similar levels and comparable to the reduction induced by the E6 prototype. The ability of the proteins to induce serum/calcium-differentiation resistant colonies in primary keratinocytes was more variable. Overall activities of the variants ranged between 0.24- and 2.18-fold of the E6 prototype activity. The I27R/L83V variant showed the lowest activity whereas the R8Q variant showed the highest activity. The L83V polymorphism previously associated with risk for cancer progression in some populations, showed significant activity, comparable to that of the E6 prototype, in reducing p53 and Bax levels. Furthermore, this variant showed enhancement in the ability to induce colonies resistant to serum/calcium-triggered differentiation, however, the difference from the prototype was not statistically significant. This, and augmentation of other described functions might result in differences in L83V pathogenicity.

MeSH Terms
Animals Cell Line, Transformed Cells, Cultured Down-Regulation Genetic Variation Human papillomavirus 16/classification,genetics,metabolism,pathogenicity Humans Keratinocytes/cytology,metabolism Mice NIH 3T3 Cells Oncogene Proteins, Viral/genetics,metabolism Polymorphism, Genetic Repressor Proteins/genetics,metabolism Tumor Suppressor Protein p53/metabolism bcl-2-Associated X Protein/metabolism
Chemicals
E6 protein, Human papillomavirus type 16 Oncogene Proteins, Viral Repressor Proteins Tumor Suppressor Protein p53 bcl-2-Associated X Protein
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Asadurian Yulia
Department of Human Microbiology, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Kurilin Helena
Lichtig Hava
Jackman Anna
Gonen Pinhas
Tommasino Massimo
Zehbe Ingeborg
Sherman Levana
Article Info
Journal
Journal of medical virology
Abbr.
J Med Virol
ISSN
0146-6615
Published
2007-11-00
Pages
1751-60
Language
English
Region
United States
NLM ID
7705876
Subset
IM
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