Cargando…
Contributions of viral oncogenes of HPV-18 and hypoxia to oxidative stress and genetic damage in human keratinocytes
Infection with high-risk human papillomaviruses like HPV-16 and HPV-18 is highly associated with the development of cervical and other cancers. Malignant transformation requires viral oncoproteins E5, E6 and E7, which promote cell proliferation and increase DNA damage. Oxidative stress and hypoxia a...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584980/ https://www.ncbi.nlm.nih.gov/pubmed/37853061 http://dx.doi.org/10.1038/s41598-023-44880-3 |
_version_ | 1785122856063991808 |
---|---|
author | Hochmann, Jimena Millán, Magdalena Hernández, Paola Lafon-Hughes, Laura Aiuto, Natali D’ Silva, Alejandro Llaguno, Juan Alonso, Julia Fernández, Ariel Pereira-Prado, Vanesa Sotelo-Silveira, José Bologna-Molina, Ronell Arocena, Miguel |
author_facet | Hochmann, Jimena Millán, Magdalena Hernández, Paola Lafon-Hughes, Laura Aiuto, Natali D’ Silva, Alejandro Llaguno, Juan Alonso, Julia Fernández, Ariel Pereira-Prado, Vanesa Sotelo-Silveira, José Bologna-Molina, Ronell Arocena, Miguel |
author_sort | Hochmann, Jimena |
collection | PubMed |
description | Infection with high-risk human papillomaviruses like HPV-16 and HPV-18 is highly associated with the development of cervical and other cancers. Malignant transformation requires viral oncoproteins E5, E6 and E7, which promote cell proliferation and increase DNA damage. Oxidative stress and hypoxia are also key factors in cervical malignant transformation. Increased levels of reactive species of oxygen (ROS) and nitrogen (RNS) are found in the hypoxic tumor microenvironment, promoting genetic instability and invasiveness. In this work, we studied the combined effect of E5, E6 and E7 and hypoxia in increasing oxidative stress and promoting DNA damage and nuclear architecture alterations. HaCaT cells containing HPV-18 viral oncogenes (HaCaT E5/E6/E7-18) showed higher ROS levels in normoxia and higher levels of RNS in hypoxia compared to HaCaT parental cells, as well as higher genetic damage in hypoxia as measured by γH2AX and comet assays. In hypoxia, HaCaT E5/E6/E7-18 increased its nuclear dry mass and both cell types displayed marked heterogeneity in nuclear dry mass distribution and increased nuclear foci. Our results show contributions of both viral oncogenes and hypoxia to oxidative stress, DNA damage and altered nuclear architecture, exemplifying how an altered microenvironment combines with oncogenic transformation to promote tumor progression. |
format | Online Article Text |
id | pubmed-10584980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105849802023-10-20 Contributions of viral oncogenes of HPV-18 and hypoxia to oxidative stress and genetic damage in human keratinocytes Hochmann, Jimena Millán, Magdalena Hernández, Paola Lafon-Hughes, Laura Aiuto, Natali D’ Silva, Alejandro Llaguno, Juan Alonso, Julia Fernández, Ariel Pereira-Prado, Vanesa Sotelo-Silveira, José Bologna-Molina, Ronell Arocena, Miguel Sci Rep Article Infection with high-risk human papillomaviruses like HPV-16 and HPV-18 is highly associated with the development of cervical and other cancers. Malignant transformation requires viral oncoproteins E5, E6 and E7, which promote cell proliferation and increase DNA damage. Oxidative stress and hypoxia are also key factors in cervical malignant transformation. Increased levels of reactive species of oxygen (ROS) and nitrogen (RNS) are found in the hypoxic tumor microenvironment, promoting genetic instability and invasiveness. In this work, we studied the combined effect of E5, E6 and E7 and hypoxia in increasing oxidative stress and promoting DNA damage and nuclear architecture alterations. HaCaT cells containing HPV-18 viral oncogenes (HaCaT E5/E6/E7-18) showed higher ROS levels in normoxia and higher levels of RNS in hypoxia compared to HaCaT parental cells, as well as higher genetic damage in hypoxia as measured by γH2AX and comet assays. In hypoxia, HaCaT E5/E6/E7-18 increased its nuclear dry mass and both cell types displayed marked heterogeneity in nuclear dry mass distribution and increased nuclear foci. Our results show contributions of both viral oncogenes and hypoxia to oxidative stress, DNA damage and altered nuclear architecture, exemplifying how an altered microenvironment combines with oncogenic transformation to promote tumor progression. Nature Publishing Group UK 2023-10-18 /pmc/articles/PMC10584980/ /pubmed/37853061 http://dx.doi.org/10.1038/s41598-023-44880-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hochmann, Jimena Millán, Magdalena Hernández, Paola Lafon-Hughes, Laura Aiuto, Natali D’ Silva, Alejandro Llaguno, Juan Alonso, Julia Fernández, Ariel Pereira-Prado, Vanesa Sotelo-Silveira, José Bologna-Molina, Ronell Arocena, Miguel Contributions of viral oncogenes of HPV-18 and hypoxia to oxidative stress and genetic damage in human keratinocytes |
title | Contributions of viral oncogenes of HPV-18 and hypoxia to oxidative stress and genetic damage in human keratinocytes |
title_full | Contributions of viral oncogenes of HPV-18 and hypoxia to oxidative stress and genetic damage in human keratinocytes |
title_fullStr | Contributions of viral oncogenes of HPV-18 and hypoxia to oxidative stress and genetic damage in human keratinocytes |
title_full_unstemmed | Contributions of viral oncogenes of HPV-18 and hypoxia to oxidative stress and genetic damage in human keratinocytes |
title_short | Contributions of viral oncogenes of HPV-18 and hypoxia to oxidative stress and genetic damage in human keratinocytes |
title_sort | contributions of viral oncogenes of hpv-18 and hypoxia to oxidative stress and genetic damage in human keratinocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584980/ https://www.ncbi.nlm.nih.gov/pubmed/37853061 http://dx.doi.org/10.1038/s41598-023-44880-3 |
work_keys_str_mv | AT hochmannjimena contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT millanmagdalena contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT hernandezpaola contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT lafonhugheslaura contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT aiutonatalid contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT silvaalejandro contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT llagunojuan contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT alonsojulia contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT fernandezariel contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT pereirapradovanesa contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT sotelosilveirajose contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT bolognamolinaronell contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes AT arocenamiguel contributionsofviraloncogenesofhpv18andhypoxiatooxidativestressandgeneticdamageinhumankeratinocytes |