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Low expression levels of putative HPV encoded microRNAs in cervical samples

Using small RNA sequencing of libraries established from cervical samples and cervical cancer cell lines, we have previously reported identification of nine and validation of five putative microRNA species encoded by human papillomaviruses (HPV) including five microRNAs encoded by HPV 16. Here we ha...

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Autores principales: Virtanen, Elina, Pietilä, Tuuli, Nieminen, Pekka, Qian, Kui, Auvinen, Eeva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075338/
https://www.ncbi.nlm.nih.gov/pubmed/27818894
http://dx.doi.org/10.1186/s40064-016-3524-3
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author Virtanen, Elina
Pietilä, Tuuli
Nieminen, Pekka
Qian, Kui
Auvinen, Eeva
author_facet Virtanen, Elina
Pietilä, Tuuli
Nieminen, Pekka
Qian, Kui
Auvinen, Eeva
author_sort Virtanen, Elina
collection PubMed
description Using small RNA sequencing of libraries established from cervical samples and cervical cancer cell lines, we have previously reported identification of nine and validation of five putative microRNA species encoded by human papillomaviruses (HPV) including five microRNAs encoded by HPV 16. Here we have studied the expression of HPV 16 encoded microRNAs in cervical samples and in HPV 16 containing cell lines. Different sample matrices were collected for the study: 20 paraffin embedded cervical tissue samples, 16 liquid cytology samples, and 16 cervical cell samples from women attending colposcopy due to cervical abnormalities, as well as four HPV 16 containing cell lines. Total RNA was extracted, the samples were spiked with small synthetic control RNAs, and the expression of five HPV 16 encoded microRNAs was assessed by real-time PCR amplification. HPV encoded microRNAs could be frequently detected, albeit at high cycle counts. HPV16-miR-H1 was detected in 3.6 %, HPV16-miR-H3 in 23.6 %, HPV16-miR-H5 in 7.3 %, and HPV16-miR-H6 in 18.2 % of all valid samples. True positive signals for HPV16-miR-H2 could not be detected in any of the samples. Viral microRNAs were detected most frequently in paraffin-embedded samples: in one sample representing normal squamous epithelium, in one cervical intraepithelial neoplasia (CIN) grade 1, one CIN2, three CIN3, two squamous cell carcinoma, three adenocarcinoma in situ, and two adenocarcinoma samples. One liquid cytology sample from a patient with CIN3 as well as all four cell lines were positive for HPV16-miR-H3. In all cases HPV encoded microRNAs were expressed at low levels. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40064-016-3524-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-50753382016-11-04 Low expression levels of putative HPV encoded microRNAs in cervical samples Virtanen, Elina Pietilä, Tuuli Nieminen, Pekka Qian, Kui Auvinen, Eeva Springerplus Research Using small RNA sequencing of libraries established from cervical samples and cervical cancer cell lines, we have previously reported identification of nine and validation of five putative microRNA species encoded by human papillomaviruses (HPV) including five microRNAs encoded by HPV 16. Here we have studied the expression of HPV 16 encoded microRNAs in cervical samples and in HPV 16 containing cell lines. Different sample matrices were collected for the study: 20 paraffin embedded cervical tissue samples, 16 liquid cytology samples, and 16 cervical cell samples from women attending colposcopy due to cervical abnormalities, as well as four HPV 16 containing cell lines. Total RNA was extracted, the samples were spiked with small synthetic control RNAs, and the expression of five HPV 16 encoded microRNAs was assessed by real-time PCR amplification. HPV encoded microRNAs could be frequently detected, albeit at high cycle counts. HPV16-miR-H1 was detected in 3.6 %, HPV16-miR-H3 in 23.6 %, HPV16-miR-H5 in 7.3 %, and HPV16-miR-H6 in 18.2 % of all valid samples. True positive signals for HPV16-miR-H2 could not be detected in any of the samples. Viral microRNAs were detected most frequently in paraffin-embedded samples: in one sample representing normal squamous epithelium, in one cervical intraepithelial neoplasia (CIN) grade 1, one CIN2, three CIN3, two squamous cell carcinoma, three adenocarcinoma in situ, and two adenocarcinoma samples. One liquid cytology sample from a patient with CIN3 as well as all four cell lines were positive for HPV16-miR-H3. In all cases HPV encoded microRNAs were expressed at low levels. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40064-016-3524-3) contains supplementary material, which is available to authorized users. Springer International Publishing 2016-10-22 /pmc/articles/PMC5075338/ /pubmed/27818894 http://dx.doi.org/10.1186/s40064-016-3524-3 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.
spellingShingle Research
Virtanen, Elina
Pietilä, Tuuli
Nieminen, Pekka
Qian, Kui
Auvinen, Eeva
Low expression levels of putative HPV encoded microRNAs in cervical samples
title Low expression levels of putative HPV encoded microRNAs in cervical samples
title_full Low expression levels of putative HPV encoded microRNAs in cervical samples
title_fullStr Low expression levels of putative HPV encoded microRNAs in cervical samples
title_full_unstemmed Low expression levels of putative HPV encoded microRNAs in cervical samples
title_short Low expression levels of putative HPV encoded microRNAs in cervical samples
title_sort low expression levels of putative hpv encoded micrornas in cervical samples
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075338/
https://www.ncbi.nlm.nih.gov/pubmed/27818894
http://dx.doi.org/10.1186/s40064-016-3524-3
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