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Episomal HPV16 responsible for aggressive and deadly metastatic anal squamous cell carcinoma evidenced in peripheral blood

Archival tissue samples collected longitudinally from a patient who died from HPV16-induced high-grade anal intraepithelial squamous cell carcinoma with vertebral HPV16–positive metastasis were retrospectively analyzed by the Capture-HPV method (Capt-HPV) followed by Next-Generation Sequencing (NGS)...

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Autores principales: Péré, Hélène, Vernet, Raphael, Pernot, Simon, Pavie, Juliette, Robillard, Nicolas, Puech, Julien, Lameiras, Sonia, Lucas, Marie-Laure, Nicolas, Alain, Badoual, Cécile, Rance, Bastien, Bélec, Laurent, Weiss, Laurence, Wack, Maxime, Veyer, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907240/
https://www.ncbi.nlm.nih.gov/pubmed/33633240
http://dx.doi.org/10.1038/s41598-021-84110-2
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author Péré, Hélène
Vernet, Raphael
Pernot, Simon
Pavie, Juliette
Robillard, Nicolas
Puech, Julien
Lameiras, Sonia
Lucas, Marie-Laure
Nicolas, Alain
Badoual, Cécile
Rance, Bastien
Bélec, Laurent
Weiss, Laurence
Wack, Maxime
Veyer, David
author_facet Péré, Hélène
Vernet, Raphael
Pernot, Simon
Pavie, Juliette
Robillard, Nicolas
Puech, Julien
Lameiras, Sonia
Lucas, Marie-Laure
Nicolas, Alain
Badoual, Cécile
Rance, Bastien
Bélec, Laurent
Weiss, Laurence
Wack, Maxime
Veyer, David
author_sort Péré, Hélène
collection PubMed
description Archival tissue samples collected longitudinally from a patient who died from HPV16-induced high-grade anal intraepithelial squamous cell carcinoma with vertebral HPV16–positive metastasis were retrospectively analyzed by the Capture-HPV method (Capt-HPV) followed by Next-Generation Sequencing (NGS). Full length nucleotide sequences of the same HPV16 were identified from the initial and second anal biopsy samples, from plasma sample and from vertebral metastasis biopsy. Remarkably, HPV was episomal in each sample. The HPV genome sequence was closest to the HPV16 Qv18158E variant subtype (A1 lineage) exhibiting base substitutions and deletions in 7 and 2 HPV loci, respectively. In conclusion, the powerful Capt-HPV followed by NGS allows evidencing the detailed cartography of tumoral and circulating HPV DNA, giving rise to a unique and unexpected episomal virus molecular status in a context of aggressive carcinoma, underlying the importance of HPV status and its association with clinical features for further prospective studies.
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spelling pubmed-79072402021-03-02 Episomal HPV16 responsible for aggressive and deadly metastatic anal squamous cell carcinoma evidenced in peripheral blood Péré, Hélène Vernet, Raphael Pernot, Simon Pavie, Juliette Robillard, Nicolas Puech, Julien Lameiras, Sonia Lucas, Marie-Laure Nicolas, Alain Badoual, Cécile Rance, Bastien Bélec, Laurent Weiss, Laurence Wack, Maxime Veyer, David Sci Rep Article Archival tissue samples collected longitudinally from a patient who died from HPV16-induced high-grade anal intraepithelial squamous cell carcinoma with vertebral HPV16–positive metastasis were retrospectively analyzed by the Capture-HPV method (Capt-HPV) followed by Next-Generation Sequencing (NGS). Full length nucleotide sequences of the same HPV16 were identified from the initial and second anal biopsy samples, from plasma sample and from vertebral metastasis biopsy. Remarkably, HPV was episomal in each sample. The HPV genome sequence was closest to the HPV16 Qv18158E variant subtype (A1 lineage) exhibiting base substitutions and deletions in 7 and 2 HPV loci, respectively. In conclusion, the powerful Capt-HPV followed by NGS allows evidencing the detailed cartography of tumoral and circulating HPV DNA, giving rise to a unique and unexpected episomal virus molecular status in a context of aggressive carcinoma, underlying the importance of HPV status and its association with clinical features for further prospective studies. Nature Publishing Group UK 2021-02-25 /pmc/articles/PMC7907240/ /pubmed/33633240 http://dx.doi.org/10.1038/s41598-021-84110-2 Text en © The Author(s) 2021 Open Access 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Péré, Hélène
Vernet, Raphael
Pernot, Simon
Pavie, Juliette
Robillard, Nicolas
Puech, Julien
Lameiras, Sonia
Lucas, Marie-Laure
Nicolas, Alain
Badoual, Cécile
Rance, Bastien
Bélec, Laurent
Weiss, Laurence
Wack, Maxime
Veyer, David
Episomal HPV16 responsible for aggressive and deadly metastatic anal squamous cell carcinoma evidenced in peripheral blood
title Episomal HPV16 responsible for aggressive and deadly metastatic anal squamous cell carcinoma evidenced in peripheral blood
title_full Episomal HPV16 responsible for aggressive and deadly metastatic anal squamous cell carcinoma evidenced in peripheral blood
title_fullStr Episomal HPV16 responsible for aggressive and deadly metastatic anal squamous cell carcinoma evidenced in peripheral blood
title_full_unstemmed Episomal HPV16 responsible for aggressive and deadly metastatic anal squamous cell carcinoma evidenced in peripheral blood
title_short Episomal HPV16 responsible for aggressive and deadly metastatic anal squamous cell carcinoma evidenced in peripheral blood
title_sort episomal hpv16 responsible for aggressive and deadly metastatic anal squamous cell carcinoma evidenced in peripheral blood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907240/
https://www.ncbi.nlm.nih.gov/pubmed/33633240
http://dx.doi.org/10.1038/s41598-021-84110-2
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