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Retrieval of HPV oncogenes E6 and E7 mRNA from cervical specimens using a manual open technology protocol

BACKGROUND: HPV oncogenes mRNA detection gains momentum as an adjuvant for HPV-related cervical abnormalities diagnosis, but is based on costly detection assays not allowing viral type targeting. OBJECTIVE: To assess detection rate of HPV oncogenes E6/E7 mRNA from cervical specimens using a manual,...

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Autores principales: Campbell, Leonardo Martins, Pitta, Denise Rocha, De Assis, Angela Maria, Derchain, Sophie Francoise Mauricette, Campos, Elisabete Aparecida, Sarian, Luis Otavio Zanatta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3795203/
https://www.ncbi.nlm.nih.gov/pubmed/24130958
http://dx.doi.org/10.1186/2193-1801-2-473
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author Campbell, Leonardo Martins
Pitta, Denise Rocha
De Assis, Angela Maria
Derchain, Sophie Francoise Mauricette
Campos, Elisabete Aparecida
Sarian, Luis Otavio Zanatta
author_facet Campbell, Leonardo Martins
Pitta, Denise Rocha
De Assis, Angela Maria
Derchain, Sophie Francoise Mauricette
Campos, Elisabete Aparecida
Sarian, Luis Otavio Zanatta
author_sort Campbell, Leonardo Martins
collection PubMed
description BACKGROUND: HPV oncogenes mRNA detection gains momentum as an adjuvant for HPV-related cervical abnormalities diagnosis, but is based on costly detection assays not allowing viral type targeting. OBJECTIVE: To assess detection rate of HPV oncogenes E6/E7 mRNA from cervical specimens using a manual, open technology, fully customizable protocol and determine whether HPV-related epidemiological features influence mRNA retrieval. We reviewed literature and compared our retrieval rate with automated technologies. METHODS: We used 60 samples positive for HPV DNA types 16, 18, 31 and/or 45. We extracted mRNA with a TRizol-based protocol, and tested mRNA purity and concentration using light absorbance. We reverse-transcribed mRNA into cDNA for E6/7 detection. RESULTS: HPV oncogenes E6/E7 mRNA was retrieved from 36 (60%) out of 60 specimens. No HPV load-related clinical or epidemiological feature was significantly associated with mRNA retrieval. Presence of HPV-DNA 16/18 was associated with mRNA retrieval (OR = 9.08; 95% CI 1.26 to 65.32 for HPV 16; and 18.2; IC95% 1.86 to 391.44 for HPV 18). CONCLUSIONS: The open-technology protocol yielded an mRNA detection rate similar to that of automated technologies. Advantages are lower costs and target HPV type customization.
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spelling pubmed-37952032013-10-15 Retrieval of HPV oncogenes E6 and E7 mRNA from cervical specimens using a manual open technology protocol Campbell, Leonardo Martins Pitta, Denise Rocha De Assis, Angela Maria Derchain, Sophie Francoise Mauricette Campos, Elisabete Aparecida Sarian, Luis Otavio Zanatta Springerplus Research BACKGROUND: HPV oncogenes mRNA detection gains momentum as an adjuvant for HPV-related cervical abnormalities diagnosis, but is based on costly detection assays not allowing viral type targeting. OBJECTIVE: To assess detection rate of HPV oncogenes E6/E7 mRNA from cervical specimens using a manual, open technology, fully customizable protocol and determine whether HPV-related epidemiological features influence mRNA retrieval. We reviewed literature and compared our retrieval rate with automated technologies. METHODS: We used 60 samples positive for HPV DNA types 16, 18, 31 and/or 45. We extracted mRNA with a TRizol-based protocol, and tested mRNA purity and concentration using light absorbance. We reverse-transcribed mRNA into cDNA for E6/7 detection. RESULTS: HPV oncogenes E6/E7 mRNA was retrieved from 36 (60%) out of 60 specimens. No HPV load-related clinical or epidemiological feature was significantly associated with mRNA retrieval. Presence of HPV-DNA 16/18 was associated with mRNA retrieval (OR = 9.08; 95% CI 1.26 to 65.32 for HPV 16; and 18.2; IC95% 1.86 to 391.44 for HPV 18). CONCLUSIONS: The open-technology protocol yielded an mRNA detection rate similar to that of automated technologies. Advantages are lower costs and target HPV type customization. Springer International Publishing 2013-09-18 /pmc/articles/PMC3795203/ /pubmed/24130958 http://dx.doi.org/10.1186/2193-1801-2-473 Text en © Campbell et al.; licensee Springer. 2013 This article is published under license to BioMed Central Ltd. 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
Campbell, Leonardo Martins
Pitta, Denise Rocha
De Assis, Angela Maria
Derchain, Sophie Francoise Mauricette
Campos, Elisabete Aparecida
Sarian, Luis Otavio Zanatta
Retrieval of HPV oncogenes E6 and E7 mRNA from cervical specimens using a manual open technology protocol
title Retrieval of HPV oncogenes E6 and E7 mRNA from cervical specimens using a manual open technology protocol
title_full Retrieval of HPV oncogenes E6 and E7 mRNA from cervical specimens using a manual open technology protocol
title_fullStr Retrieval of HPV oncogenes E6 and E7 mRNA from cervical specimens using a manual open technology protocol
title_full_unstemmed Retrieval of HPV oncogenes E6 and E7 mRNA from cervical specimens using a manual open technology protocol
title_short Retrieval of HPV oncogenes E6 and E7 mRNA from cervical specimens using a manual open technology protocol
title_sort retrieval of hpv oncogenes e6 and e7 mrna from cervical specimens using a manual open technology protocol
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3795203/
https://www.ncbi.nlm.nih.gov/pubmed/24130958
http://dx.doi.org/10.1186/2193-1801-2-473
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