Cargando…

Conditional Cell Reprogramming and Air–Liquid Interface Modeling Life Cycle of Oncogenic Viruses (HPV and EBV) in Epithelial Cells and Virus-Associated Human Carcinomas

Several oncogenic viruses are associated with approximately 20% of human cancers. Experimental models are crucial for studying the pathogenicity and biological aspects of oncogenic viruses and their potential mechanisms in tumorigenesis. Current cell models have considerable limitations such as: the...

Descripción completa

Detalles Bibliográficos
Autores principales: Rani, Abdul Qawee, Nurmemet, Dilber, Liffick, Joseph, Khan, Anam, Mitchell, Darrion, Li, Jenny, Zhao, Bo, Liu, Xuefeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302659/
https://www.ncbi.nlm.nih.gov/pubmed/37376685
http://dx.doi.org/10.3390/v15061388
_version_ 1785065095691239424
author Rani, Abdul Qawee
Nurmemet, Dilber
Liffick, Joseph
Khan, Anam
Mitchell, Darrion
Li, Jenny
Zhao, Bo
Liu, Xuefeng
author_facet Rani, Abdul Qawee
Nurmemet, Dilber
Liffick, Joseph
Khan, Anam
Mitchell, Darrion
Li, Jenny
Zhao, Bo
Liu, Xuefeng
author_sort Rani, Abdul Qawee
collection PubMed
description Several oncogenic viruses are associated with approximately 20% of human cancers. Experimental models are crucial for studying the pathogenicity and biological aspects of oncogenic viruses and their potential mechanisms in tumorigenesis. Current cell models have considerable limitations such as: their low yield, genetic and epigenetic modification, and reduction in tumor heterogeneity during long propagation. Cancer cell lines are limited and not appropriate for studying the viral life cycle, for example, natural viral life cycles of HPV and EBV, and their persistence and latency in epithelial cells are poorly understood, since these processes are highly related to epithelial differentiation. Therefore, there is an urgent need of reliable human physiological cell models to study viral life cycle and cancer initiation. Conditional cell reprogramming (CCR) is a rapid and robust cell culture system, where the cells can be established from minimally invasive or noninvasive specimens and their lineage functions preserved during the long-term culture. These CR cells retain their ability to differentiate at air–liquid interface (ALI). Here, we recapitulated the applications of CR and ALI approaches in modeling host–virus interactions and viral-mediated tumorigenesis.
format Online
Article
Text
id pubmed-10302659
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-103026592023-06-29 Conditional Cell Reprogramming and Air–Liquid Interface Modeling Life Cycle of Oncogenic Viruses (HPV and EBV) in Epithelial Cells and Virus-Associated Human Carcinomas Rani, Abdul Qawee Nurmemet, Dilber Liffick, Joseph Khan, Anam Mitchell, Darrion Li, Jenny Zhao, Bo Liu, Xuefeng Viruses Review Several oncogenic viruses are associated with approximately 20% of human cancers. Experimental models are crucial for studying the pathogenicity and biological aspects of oncogenic viruses and their potential mechanisms in tumorigenesis. Current cell models have considerable limitations such as: their low yield, genetic and epigenetic modification, and reduction in tumor heterogeneity during long propagation. Cancer cell lines are limited and not appropriate for studying the viral life cycle, for example, natural viral life cycles of HPV and EBV, and their persistence and latency in epithelial cells are poorly understood, since these processes are highly related to epithelial differentiation. Therefore, there is an urgent need of reliable human physiological cell models to study viral life cycle and cancer initiation. Conditional cell reprogramming (CCR) is a rapid and robust cell culture system, where the cells can be established from minimally invasive or noninvasive specimens and their lineage functions preserved during the long-term culture. These CR cells retain their ability to differentiate at air–liquid interface (ALI). Here, we recapitulated the applications of CR and ALI approaches in modeling host–virus interactions and viral-mediated tumorigenesis. MDPI 2023-06-17 /pmc/articles/PMC10302659/ /pubmed/37376685 http://dx.doi.org/10.3390/v15061388 Text en © 2023 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 Review
Rani, Abdul Qawee
Nurmemet, Dilber
Liffick, Joseph
Khan, Anam
Mitchell, Darrion
Li, Jenny
Zhao, Bo
Liu, Xuefeng
Conditional Cell Reprogramming and Air–Liquid Interface Modeling Life Cycle of Oncogenic Viruses (HPV and EBV) in Epithelial Cells and Virus-Associated Human Carcinomas
title Conditional Cell Reprogramming and Air–Liquid Interface Modeling Life Cycle of Oncogenic Viruses (HPV and EBV) in Epithelial Cells and Virus-Associated Human Carcinomas
title_full Conditional Cell Reprogramming and Air–Liquid Interface Modeling Life Cycle of Oncogenic Viruses (HPV and EBV) in Epithelial Cells and Virus-Associated Human Carcinomas
title_fullStr Conditional Cell Reprogramming and Air–Liquid Interface Modeling Life Cycle of Oncogenic Viruses (HPV and EBV) in Epithelial Cells and Virus-Associated Human Carcinomas
title_full_unstemmed Conditional Cell Reprogramming and Air–Liquid Interface Modeling Life Cycle of Oncogenic Viruses (HPV and EBV) in Epithelial Cells and Virus-Associated Human Carcinomas
title_short Conditional Cell Reprogramming and Air–Liquid Interface Modeling Life Cycle of Oncogenic Viruses (HPV and EBV) in Epithelial Cells and Virus-Associated Human Carcinomas
title_sort conditional cell reprogramming and air–liquid interface modeling life cycle of oncogenic viruses (hpv and ebv) in epithelial cells and virus-associated human carcinomas
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302659/
https://www.ncbi.nlm.nih.gov/pubmed/37376685
http://dx.doi.org/10.3390/v15061388
work_keys_str_mv AT raniabdulqawee conditionalcellreprogrammingandairliquidinterfacemodelinglifecycleofoncogenicviruseshpvandebvinepithelialcellsandvirusassociatedhumancarcinomas
AT nurmemetdilber conditionalcellreprogrammingandairliquidinterfacemodelinglifecycleofoncogenicviruseshpvandebvinepithelialcellsandvirusassociatedhumancarcinomas
AT liffickjoseph conditionalcellreprogrammingandairliquidinterfacemodelinglifecycleofoncogenicviruseshpvandebvinepithelialcellsandvirusassociatedhumancarcinomas
AT khananam conditionalcellreprogrammingandairliquidinterfacemodelinglifecycleofoncogenicviruseshpvandebvinepithelialcellsandvirusassociatedhumancarcinomas
AT mitchelldarrion conditionalcellreprogrammingandairliquidinterfacemodelinglifecycleofoncogenicviruseshpvandebvinepithelialcellsandvirusassociatedhumancarcinomas
AT lijenny conditionalcellreprogrammingandairliquidinterfacemodelinglifecycleofoncogenicviruseshpvandebvinepithelialcellsandvirusassociatedhumancarcinomas
AT zhaobo conditionalcellreprogrammingandairliquidinterfacemodelinglifecycleofoncogenicviruseshpvandebvinepithelialcellsandvirusassociatedhumancarcinomas
AT liuxuefeng conditionalcellreprogrammingandairliquidinterfacemodelinglifecycleofoncogenicviruseshpvandebvinepithelialcellsandvirusassociatedhumancarcinomas