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Effects of human papillomavirus (HPV) type 16 oncoproteins on the expression of involucrin in human keratinocytes
BACKGROUND: The human papillomavirus (HPV) life cycle is closely linked to keratinocyte differentiation. Oncogenic HPV infection has been shown to hamper the normal differentiation of keratinocytes; however, the underlying mechanisms responsible for this phenomenon are yet to be clarified. Here, we...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296608/ https://www.ncbi.nlm.nih.gov/pubmed/22333115 http://dx.doi.org/10.1186/1743-422X-9-36 |
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author | Gyöngyösi, Eszter Szalmás, Anita Ferenczi, Annamária Kónya, József Gergely, Lajos Veress, György |
author_facet | Gyöngyösi, Eszter Szalmás, Anita Ferenczi, Annamária Kónya, József Gergely, Lajos Veress, György |
author_sort | Gyöngyösi, Eszter |
collection | PubMed |
description | BACKGROUND: The human papillomavirus (HPV) life cycle is closely linked to keratinocyte differentiation. Oncogenic HPV infection has been shown to hamper the normal differentiation of keratinocytes; however, the underlying mechanisms responsible for this phenomenon are yet to be clarified. Here, we aimed to study the effects of HPV16 E6 and E7 oncogenes on the expression of involucrin (IVL), an established marker of keratinocyte differentiation, in human foreskin keratinocyte (HFK) cells. RESULTS: The differentiation of HFK cells by serum and high calcium significantly increased both the mRNA and the protein levels of IVL. The E6 and E7 oncoproteins of HPV16 together caused strong down-regulation of IVL mRNA and protein both in proliferating and in differentiating HFK cells. To study the effects of HPV oncogenes on the IVL promoter, we made transient transfection assays and luciferase tests and found that HPV 16 E6 but not E7 repressed IVL promoter activity in proliferating HFK cells. The inhibitory effect of HPV 16 E6 on the human IVL promoter could be localised to the proximal regulatory region (PRR) of the gene. CONCLUSIONS: These results suggest that the down-regulation of IVL promoter activity by HPV 16 E6 significantly contribute to the inhibition of endogenous IVL expression by the HPV 16 oncoproteins. In contrast, the down-regulation of endogenous IVL expression by HPV16 E7 is probably not caused by a direct and specific effect of E7 on the IVL promoter. |
format | Online Article Text |
id | pubmed-3296608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32966082012-03-08 Effects of human papillomavirus (HPV) type 16 oncoproteins on the expression of involucrin in human keratinocytes Gyöngyösi, Eszter Szalmás, Anita Ferenczi, Annamária Kónya, József Gergely, Lajos Veress, György Virol J Research BACKGROUND: The human papillomavirus (HPV) life cycle is closely linked to keratinocyte differentiation. Oncogenic HPV infection has been shown to hamper the normal differentiation of keratinocytes; however, the underlying mechanisms responsible for this phenomenon are yet to be clarified. Here, we aimed to study the effects of HPV16 E6 and E7 oncogenes on the expression of involucrin (IVL), an established marker of keratinocyte differentiation, in human foreskin keratinocyte (HFK) cells. RESULTS: The differentiation of HFK cells by serum and high calcium significantly increased both the mRNA and the protein levels of IVL. The E6 and E7 oncoproteins of HPV16 together caused strong down-regulation of IVL mRNA and protein both in proliferating and in differentiating HFK cells. To study the effects of HPV oncogenes on the IVL promoter, we made transient transfection assays and luciferase tests and found that HPV 16 E6 but not E7 repressed IVL promoter activity in proliferating HFK cells. The inhibitory effect of HPV 16 E6 on the human IVL promoter could be localised to the proximal regulatory region (PRR) of the gene. CONCLUSIONS: These results suggest that the down-regulation of IVL promoter activity by HPV 16 E6 significantly contribute to the inhibition of endogenous IVL expression by the HPV 16 oncoproteins. In contrast, the down-regulation of endogenous IVL expression by HPV16 E7 is probably not caused by a direct and specific effect of E7 on the IVL promoter. BioMed Central 2012-02-14 /pmc/articles/PMC3296608/ /pubmed/22333115 http://dx.doi.org/10.1186/1743-422X-9-36 Text en Copyright ©2012 Gyöngyösi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Gyöngyösi, Eszter Szalmás, Anita Ferenczi, Annamária Kónya, József Gergely, Lajos Veress, György Effects of human papillomavirus (HPV) type 16 oncoproteins on the expression of involucrin in human keratinocytes |
title | Effects of human papillomavirus (HPV) type 16 oncoproteins on the expression of involucrin in human keratinocytes |
title_full | Effects of human papillomavirus (HPV) type 16 oncoproteins on the expression of involucrin in human keratinocytes |
title_fullStr | Effects of human papillomavirus (HPV) type 16 oncoproteins on the expression of involucrin in human keratinocytes |
title_full_unstemmed | Effects of human papillomavirus (HPV) type 16 oncoproteins on the expression of involucrin in human keratinocytes |
title_short | Effects of human papillomavirus (HPV) type 16 oncoproteins on the expression of involucrin in human keratinocytes |
title_sort | effects of human papillomavirus (hpv) type 16 oncoproteins on the expression of involucrin in human keratinocytes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296608/ https://www.ncbi.nlm.nih.gov/pubmed/22333115 http://dx.doi.org/10.1186/1743-422X-9-36 |
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