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Type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (CIN)
A series of 176 archival cervical intraepithelial neoplasia (CIN) was analysed for the presence, viral load and integration status of ‘high-risk’ types of human papillomavirus (HR-HPV). The samples were assayed using newly developed methods based on real-time PCR. Two methods for the extraction of D...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361820/ https://www.ncbi.nlm.nih.gov/pubmed/15942630 http://dx.doi.org/10.1038/sj.bjc.6602648 |
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author | Andersson, S Safari, H Mints, M Lewensohn- Fuchs, I Gyllensten, U Johansson, B |
author_facet | Andersson, S Safari, H Mints, M Lewensohn- Fuchs, I Gyllensten, U Johansson, B |
author_sort | Andersson, S |
collection | PubMed |
description | A series of 176 archival cervical intraepithelial neoplasia (CIN) was analysed for the presence, viral load and integration status of ‘high-risk’ types of human papillomavirus (HR-HPV). The samples were assayed using newly developed methods based on real-time PCR. Two methods for the extraction of DNA from the paraffin-embedded biopsies were compared: a protocol based on the MagNA pure system (Roche) and a Qiagen spin column kit (Qiagen). It was possible to amplify 94% (166) of the samples. Of these, 36, 63 and 80% of the CIN I, II and III cases contained HR-HPV. HPV 16 was the most prevalent, and was found in 20, 28 and 46% of the CIN I, II and III cases, respectively. The second most frequent HR-HPV was type 33 group, and in CIN II it was as prevalent as HPV 16. The median number of copies of HR-HPV per cell was not significantly different in the CIN I, II and III cases, but there was a wide range of viral load values over several magnitudes, regardless of the grade of CIN. All samples were found to contain integrated forms of HPV 16, frequently mixed with an episomal form. |
format | Text |
id | pubmed-2361820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23618202009-09-10 Type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (CIN) Andersson, S Safari, H Mints, M Lewensohn- Fuchs, I Gyllensten, U Johansson, B Br J Cancer Molecular Diagnostics A series of 176 archival cervical intraepithelial neoplasia (CIN) was analysed for the presence, viral load and integration status of ‘high-risk’ types of human papillomavirus (HR-HPV). The samples were assayed using newly developed methods based on real-time PCR. Two methods for the extraction of DNA from the paraffin-embedded biopsies were compared: a protocol based on the MagNA pure system (Roche) and a Qiagen spin column kit (Qiagen). It was possible to amplify 94% (166) of the samples. Of these, 36, 63 and 80% of the CIN I, II and III cases contained HR-HPV. HPV 16 was the most prevalent, and was found in 20, 28 and 46% of the CIN I, II and III cases, respectively. The second most frequent HR-HPV was type 33 group, and in CIN II it was as prevalent as HPV 16. The median number of copies of HR-HPV per cell was not significantly different in the CIN I, II and III cases, but there was a wide range of viral load values over several magnitudes, regardless of the grade of CIN. All samples were found to contain integrated forms of HPV 16, frequently mixed with an episomal form. Nature Publishing Group 2005-06-20 2005-06-07 /pmc/articles/PMC2361820/ /pubmed/15942630 http://dx.doi.org/10.1038/sj.bjc.6602648 Text en Copyright © 2005 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Andersson, S Safari, H Mints, M Lewensohn- Fuchs, I Gyllensten, U Johansson, B Type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (CIN) |
title | Type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (CIN) |
title_full | Type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (CIN) |
title_fullStr | Type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (CIN) |
title_full_unstemmed | Type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (CIN) |
title_short | Type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (CIN) |
title_sort | type distribution, viral load and integration status of high-risk human papillomaviruses in pre-stages of cervical cancer (cin) |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361820/ https://www.ncbi.nlm.nih.gov/pubmed/15942630 http://dx.doi.org/10.1038/sj.bjc.6602648 |
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