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E6/E7 Functional Differences among Two Natural Human Papillomavirus 18 Variants in Human Keratinocytes

It is suggested that HPV-18 variants from the A lineage have higher oncogenic potential compared to B variants. Some studies show uneven distribution of HPV-18 variants in cervical adenocarcinomas and squamous cell carcinomas. Regarding HPV-18 variants’ functions, the few studies reported focus on E...

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Autores principales: Nunes, Emily Montosa, Talpe-Nunes, Valéria, Sobrinho, João Simão, Ferreira, Silvaneide, Lino, Vanesca de Souza, Termini, Lara, Silva, Gabriela Ávila Fernandes, Boccardo, Enrique, Villa, Luisa Lina, Sichero, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228617/
https://www.ncbi.nlm.nih.gov/pubmed/34200583
http://dx.doi.org/10.3390/v13061114
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author Nunes, Emily Montosa
Talpe-Nunes, Valéria
Sobrinho, João Simão
Ferreira, Silvaneide
Lino, Vanesca de Souza
Termini, Lara
Silva, Gabriela Ávila Fernandes
Boccardo, Enrique
Villa, Luisa Lina
Sichero, Laura
author_facet Nunes, Emily Montosa
Talpe-Nunes, Valéria
Sobrinho, João Simão
Ferreira, Silvaneide
Lino, Vanesca de Souza
Termini, Lara
Silva, Gabriela Ávila Fernandes
Boccardo, Enrique
Villa, Luisa Lina
Sichero, Laura
author_sort Nunes, Emily Montosa
collection PubMed
description It is suggested that HPV-18 variants from the A lineage have higher oncogenic potential compared to B variants. Some studies show uneven distribution of HPV-18 variants in cervical adenocarcinomas and squamous cell carcinomas. Regarding HPV-18 variants’ functions, the few studies reported focus on E6, and none were performed using natural host cells. Here, we immortalized primary human keratinocytes (PHKs) with E6/E7 of HPV-18 A1 and B1 sublineages and functionally characterized these cells. PHK18A1 reached immortalization significantly faster than PHK18B1 and formed a higher number of colonies in monolayer and 3D cultures. Moreover, PHK18A1 showed greater invasion ability and higher resistance to apoptosis induced by actinomycin-D. Nevertheless, no differences were observed regarding morphology, proliferation after immortalization, migration, or epithelial development in raft cultures. Noteworthy, our study highlights qualitative differences among HPV-18 A1 and B1 immortalized PHKs: in contrast to PHK18A1, which formed more compact colonies and spheroids of firmly grouped cells and tended to invade and migrate as clustered cells, morphologically, PHK18B1 colonies and spheroids were looser, and migration and invasion of single cells were observed. Although these observations may be relevant for the association of these variants with cervical cancer of different histological subtypes, further studies are warranted to elucidate the mechanisms behind these findings.
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spelling pubmed-82286172021-06-26 E6/E7 Functional Differences among Two Natural Human Papillomavirus 18 Variants in Human Keratinocytes Nunes, Emily Montosa Talpe-Nunes, Valéria Sobrinho, João Simão Ferreira, Silvaneide Lino, Vanesca de Souza Termini, Lara Silva, Gabriela Ávila Fernandes Boccardo, Enrique Villa, Luisa Lina Sichero, Laura Viruses Article It is suggested that HPV-18 variants from the A lineage have higher oncogenic potential compared to B variants. Some studies show uneven distribution of HPV-18 variants in cervical adenocarcinomas and squamous cell carcinomas. Regarding HPV-18 variants’ functions, the few studies reported focus on E6, and none were performed using natural host cells. Here, we immortalized primary human keratinocytes (PHKs) with E6/E7 of HPV-18 A1 and B1 sublineages and functionally characterized these cells. PHK18A1 reached immortalization significantly faster than PHK18B1 and formed a higher number of colonies in monolayer and 3D cultures. Moreover, PHK18A1 showed greater invasion ability and higher resistance to apoptosis induced by actinomycin-D. Nevertheless, no differences were observed regarding morphology, proliferation after immortalization, migration, or epithelial development in raft cultures. Noteworthy, our study highlights qualitative differences among HPV-18 A1 and B1 immortalized PHKs: in contrast to PHK18A1, which formed more compact colonies and spheroids of firmly grouped cells and tended to invade and migrate as clustered cells, morphologically, PHK18B1 colonies and spheroids were looser, and migration and invasion of single cells were observed. Although these observations may be relevant for the association of these variants with cervical cancer of different histological subtypes, further studies are warranted to elucidate the mechanisms behind these findings. MDPI 2021-06-10 /pmc/articles/PMC8228617/ /pubmed/34200583 http://dx.doi.org/10.3390/v13061114 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nunes, Emily Montosa
Talpe-Nunes, Valéria
Sobrinho, João Simão
Ferreira, Silvaneide
Lino, Vanesca de Souza
Termini, Lara
Silva, Gabriela Ávila Fernandes
Boccardo, Enrique
Villa, Luisa Lina
Sichero, Laura
E6/E7 Functional Differences among Two Natural Human Papillomavirus 18 Variants in Human Keratinocytes
title E6/E7 Functional Differences among Two Natural Human Papillomavirus 18 Variants in Human Keratinocytes
title_full E6/E7 Functional Differences among Two Natural Human Papillomavirus 18 Variants in Human Keratinocytes
title_fullStr E6/E7 Functional Differences among Two Natural Human Papillomavirus 18 Variants in Human Keratinocytes
title_full_unstemmed E6/E7 Functional Differences among Two Natural Human Papillomavirus 18 Variants in Human Keratinocytes
title_short E6/E7 Functional Differences among Two Natural Human Papillomavirus 18 Variants in Human Keratinocytes
title_sort e6/e7 functional differences among two natural human papillomavirus 18 variants in human keratinocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228617/
https://www.ncbi.nlm.nih.gov/pubmed/34200583
http://dx.doi.org/10.3390/v13061114
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