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mRNA sequencing of novel cell lines from human papillomavirus type-16 related vulval intraepithelial neoplasia: Consequences of expression of HPV16 E4 and E5

mRNA sequencing of novel cell lines from human papillomavirus type-16 related vulval intraepithelial neoplasia: Consequences of expression of HPV16 E4 and E5
mRNA sequencing of novel cell lines from human papillomavirus type-16 related vulval intraepithelial neoplasia: Consequences of expression of HPV16 E4 and E5
Vulval intraepithelial neoplasia is a precursor of vulval cancer and is commonly caused by infection with Human Papillomavirus (HPV). Development of topical treatments for vulval intraepithelial neoplasia requires appropriate in vitro models. This study evaluated the feasibility of primary culture of vulval intraepithelial neoplasia biopsy tissue to produce cell lines for use as in vitro models. A potentially immortal cell line was produced which gave rise to three monoclonal lines. These lines were characterized for HPV genomic integration and for viral gene expression using ligation-mediated PCR and quantitative PCR. Distinct patterns of viral integration and gene expression were observed among the three lines. Integration and expression data were validated using deep sequencing of mRNA. Gene ontology analyses of these data also demonstrated that expression of the HPV16 E4 and E5 proteins resulted in substantial changes in the composition of the cell membrane and extracellular space, associated with alterations in cell adhesion and differentiation. These data illustrate the diverse patterns of HPV gene expression potentially present within a single lesion. The derived cell lines provide useful models to investigate the biology of vulval intraepithelial neoplasia and the interactions between different HPV gene products and potential therapeutic agents. J. Med. Virol. 86:1534–1541, 2014. © 2014 Wiley Periodicals, Inc.
0146-6615
Bryant, D.
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Onions, T.
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Raybould, R.
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Flynn, A.
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Tristram, Amanda
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Meyrick, S.
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Giles, P.
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Ashelford, K.
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Hibbitts, S.
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Fiander, A.
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Powell, N.
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Bryant, D.
10ed83e8-8080-4d9c-bba5-df9d4eec3a10
Onions, T.
aa150d82-f113-401d-8b3e-e44fb8f83afa
Raybould, R.
e50082d7-12bb-4e64-8cc7-0a3ec3e71431
Flynn, A.
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Tristram, Amanda
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Meyrick, S.
f4a3829e-809e-4d73-9a9c-41374d413d91
Giles, P.
39b0b62f-734f-4240-a299-f81aabcf2919
Ashelford, K.
c39b32ca-350b-4a73-89f8-43c52da360ae
Hibbitts, S.
dc5bb5c9-0925-43e8-85dd-f1f8a0ac3acc
Fiander, A.
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Powell, N.
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Bryant, D., Onions, T., Raybould, R., Flynn, A., Tristram, Amanda, Meyrick, S., Giles, P., Ashelford, K., Hibbitts, S., Fiander, A. and Powell, N. (2014) mRNA sequencing of novel cell lines from human papillomavirus type-16 related vulval intraepithelial neoplasia: Consequences of expression of HPV16 E4 and E5. Journal of Medical Virology, 58 (9). (doi:10.1002/jmv.23994).

Record type: Article

Abstract

Vulval intraepithelial neoplasia is a precursor of vulval cancer and is commonly caused by infection with Human Papillomavirus (HPV). Development of topical treatments for vulval intraepithelial neoplasia requires appropriate in vitro models. This study evaluated the feasibility of primary culture of vulval intraepithelial neoplasia biopsy tissue to produce cell lines for use as in vitro models. A potentially immortal cell line was produced which gave rise to three monoclonal lines. These lines were characterized for HPV genomic integration and for viral gene expression using ligation-mediated PCR and quantitative PCR. Distinct patterns of viral integration and gene expression were observed among the three lines. Integration and expression data were validated using deep sequencing of mRNA. Gene ontology analyses of these data also demonstrated that expression of the HPV16 E4 and E5 proteins resulted in substantial changes in the composition of the cell membrane and extracellular space, associated with alterations in cell adhesion and differentiation. These data illustrate the diverse patterns of HPV gene expression potentially present within a single lesion. The derived cell lines provide useful models to investigate the biology of vulval intraepithelial neoplasia and the interactions between different HPV gene products and potential therapeutic agents. J. Med. Virol. 86:1534–1541, 2014. © 2014 Wiley Periodicals, Inc.

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e-pub ahead of print date: 5 June 2014

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Local EPrints ID: 495030
URI: http://eprints.soton.ac.uk/id/eprint/495030
ISSN: 0146-6615
PURE UUID: 8a30372f-181b-4dec-87c7-51e25129e9b6
ORCID for D. Bryant: ORCID iD orcid.org/0000-0003-3163-608X

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Date deposited: 25 Oct 2024 17:06
Last modified: 02 Nov 2024 02:48

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Contributors

Author: D. Bryant ORCID iD
Author: T. Onions
Author: R. Raybould
Author: A. Flynn
Author: Amanda Tristram
Author: S. Meyrick
Author: P. Giles
Author: K. Ashelford
Author: S. Hibbitts
Author: A. Fiander
Author: N. Powell

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