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Assessment of human papillomavirus E6/E7 oncogene expression as cervical disease biomarker
BACKGROUND: The aims of this study were to detect HPV E6/E7 mRNA expression in women with high-risk genotypes (HPV-16, -18, -31, -33 and -45) analysing its relationship with tissue pathology and 2) 2-year follow-up of E6/E7 mRNA tested group. METHODS: Our samples were genotyped and classified by pat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097850/ https://www.ncbi.nlm.nih.gov/pubmed/27816058 http://dx.doi.org/10.1186/s12885-016-2885-x |
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author | Fontecha, Nerea Basaras, Miren Hernáez, Silvia Andía, Daniel Cisterna, Ramón |
author_facet | Fontecha, Nerea Basaras, Miren Hernáez, Silvia Andía, Daniel Cisterna, Ramón |
author_sort | Fontecha, Nerea |
collection | PubMed |
description | BACKGROUND: The aims of this study were to detect HPV E6/E7 mRNA expression in women with high-risk genotypes (HPV-16, -18, -31, -33 and -45) analysing its relationship with tissue pathology and 2) 2-year follow-up of E6/E7 mRNA tested group. METHODS: Our samples were genotyped and classified by pathologists according to Bethesda system. After RNA extraction, E6/E7 oncogene mRNA detection was performed by NucliSens® EasyQ® HPV v1 Test (bioMérieux). RESULTS: The results of the present study showed that E6/E7 mRNA positivity rate was 68.29 % in women tested once and 69.56 % in women tested twice. According to tissue pathology, all samples with high-grade lesions were positive for mRNA. Among women with low-grade lesions varied over the years from 89.28 to 84 % in women tested once and from 77.77 to 70 % in tested twice. Among women without lesion, positivity rate maintained in women tested once (from 50 to 41.38 %) and decreased in tested twice, from 63.63 to 44.44 %. Regarding lesion evolution, mRNA positivity was higher in women with lesion progression (53.13 %) and in women with positive results in two tested samples (83.33 %). CONCLUSION: HPV E6/E7 mRNA detection may be an effective screening test and biomarker for cervical cancer in women infected with these five genotypes. Nonetheless, further studies are needed to standardize as routine triage test. |
format | Online Article Text |
id | pubmed-5097850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50978502016-11-08 Assessment of human papillomavirus E6/E7 oncogene expression as cervical disease biomarker Fontecha, Nerea Basaras, Miren Hernáez, Silvia Andía, Daniel Cisterna, Ramón BMC Cancer Research Article BACKGROUND: The aims of this study were to detect HPV E6/E7 mRNA expression in women with high-risk genotypes (HPV-16, -18, -31, -33 and -45) analysing its relationship with tissue pathology and 2) 2-year follow-up of E6/E7 mRNA tested group. METHODS: Our samples were genotyped and classified by pathologists according to Bethesda system. After RNA extraction, E6/E7 oncogene mRNA detection was performed by NucliSens® EasyQ® HPV v1 Test (bioMérieux). RESULTS: The results of the present study showed that E6/E7 mRNA positivity rate was 68.29 % in women tested once and 69.56 % in women tested twice. According to tissue pathology, all samples with high-grade lesions were positive for mRNA. Among women with low-grade lesions varied over the years from 89.28 to 84 % in women tested once and from 77.77 to 70 % in tested twice. Among women without lesion, positivity rate maintained in women tested once (from 50 to 41.38 %) and decreased in tested twice, from 63.63 to 44.44 %. Regarding lesion evolution, mRNA positivity was higher in women with lesion progression (53.13 %) and in women with positive results in two tested samples (83.33 %). CONCLUSION: HPV E6/E7 mRNA detection may be an effective screening test and biomarker for cervical cancer in women infected with these five genotypes. Nonetheless, further studies are needed to standardize as routine triage test. BioMed Central 2016-11-05 /pmc/articles/PMC5097850/ /pubmed/27816058 http://dx.doi.org/10.1186/s12885-016-2885-x Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Fontecha, Nerea Basaras, Miren Hernáez, Silvia Andía, Daniel Cisterna, Ramón Assessment of human papillomavirus E6/E7 oncogene expression as cervical disease biomarker |
title | Assessment of human papillomavirus E6/E7 oncogene expression as cervical disease biomarker |
title_full | Assessment of human papillomavirus E6/E7 oncogene expression as cervical disease biomarker |
title_fullStr | Assessment of human papillomavirus E6/E7 oncogene expression as cervical disease biomarker |
title_full_unstemmed | Assessment of human papillomavirus E6/E7 oncogene expression as cervical disease biomarker |
title_short | Assessment of human papillomavirus E6/E7 oncogene expression as cervical disease biomarker |
title_sort | assessment of human papillomavirus e6/e7 oncogene expression as cervical disease biomarker |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097850/ https://www.ncbi.nlm.nih.gov/pubmed/27816058 http://dx.doi.org/10.1186/s12885-016-2885-x |
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